HP:0000001	All
HP:0000002	Abnormality of body height
HP:0000003	Multicystic kidney dysplasia
HP:0000005	Mode of inheritance
HP:0000006	Autosomal dominant inheritance
HP:0000007	Autosomal recessive inheritance
HP:0000008	Abnormality of female internal genitalia
HP:0000009	Functional abnormality of the bladder
HP:0000010	Recurrent urinary tract infections
HP:0000011	Neurogenic bladder
HP:0000012	Urinary urgency
HP:0000013	Hypoplasia of the uterus
HP:0000014	Abnormality of the bladder
HP:0000015	Bladder diverticulum
HP:0000016	Urinary retention
HP:0000017	Nocturia
HP:0000019	Urinary hesitancy
HP:0000020	Urinary incontinence
HP:0000021	Megacystis
HP:0000022	Abnormality of male internal genitalia
HP:0000023	Inguinal hernia
HP:0000024	Prostatitis
HP:0000025	Functional abnormality of male internal genitalia
HP:0000026	Male hypogonadism
HP:0000027	Azoospermia
HP:0000028	Cryptorchidism
HP:0000029	Testicular atrophy
HP:0000030	Testicular gonadoblastoma
HP:0000031	Epididymitis
HP:0000032	Abnormality of male external genitalia
HP:0000033	Ambiguous genitalia, male
HP:0000034	Hydrocele testis
HP:0000035	Abnormality of the testis
HP:0000036	Abnormality of the penis
HP:0000037	Male pseudohermaphroditism
HP:0000039	Epispadias
HP:0000040	Long penis
HP:0000041	Chordee
HP:0000042	Absent external genitalia
HP:0000044	Hypogonadotrophic hypogonadism
HP:0000045	Abnormality of the scrotum
HP:0000046	Scrotal hypoplasia
HP:0000047	Hypospadias
HP:0000048	Bifid scrotum
HP:0000049	Shawl scrotum
HP:0000050	Hypoplastic male external genitalia
HP:0000051	Perineal hypospadias
HP:0000052	Urethral atresia, male
HP:0000053	Macroorchidism
HP:0000054	Micropenis
HP:0000055	Abnormality of female external genitalia
HP:0000056	Abnormality of the clitoris
HP:0000057	obsolete Clitoromegaly
HP:0000058	Abnormality of the labia
HP:0000059	Hypoplastic labia majora
HP:0000060	Clitoral hypoplasia
HP:0000061	Ambiguous genitalia, female
HP:0000062	Ambiguous genitalia
HP:0000063	Fused labia minora
HP:0000064	Hypoplastic labia minora
HP:0000065	Labial hypertrophy
HP:0000066	Labial hypoplasia
HP:0000067	Urethral atresia, female
HP:0000068	Urethral atresia
HP:0000069	Abnormality of the ureter
HP:0000070	Ureterocele
HP:0000071	Ureteral stenosis
HP:0000072	Hydroureter
HP:0000073	Ureteral duplication
HP:0000074	Ureteropelvic junction obstruction
HP:0000075	Renal duplication
HP:0000076	Vesicoureteral reflux
HP:0000077	Abnormality of the kidney
HP:0000078	Abnormality of the genital system
HP:0000079	Abnormality of the urinary system
HP:0000080	Abnormality of reproductive system physiology
HP:0000081	Duplicated collecting system
HP:0000083	Renal insufficiency
HP:0000085	Horseshoe kidney
HP:0000086	Ectopic kidney
HP:0000089	Renal hypoplasia
HP:0000090	Nephronophthisis
HP:0000091	Abnormality of the renal tubule
HP:0000092	Tubular atrophy
HP:0000093	Proteinuria
HP:0000095	Abnormality of renal glomerulus morphology
HP:0000096	Glomerulosclerosis
HP:0000097	Focal segmental glomerulosclerosis
HP:0000098	Tall stature
HP:0000099	Glomerulonephritis
HP:0000100	Nephrotic syndrome
HP:0000103	Polyuria
HP:0000104	Renal agenesis
HP:0000105	Enlarged kidney
HP:0000107	Renal cyst
HP:0000108	Renal corticomedullary cysts
HP:0000110	Renal dysplasia
HP:0000111	Renal juxtaglomerular cell hypertrophy/hyperplasia
HP:0000112	Nephropathy
HP:0000113	Polycystic kidney dysplasia
HP:0000114	Proximal tubulopathy
HP:0000117	Renal phosphate wasting
HP:0000118	Phenotypic abnormality
HP:0000119	Abnormality of the genitourinary system
HP:0000121	Nephrocalcinosis
HP:0000122	Unilateral renal agenesis
HP:0000123	Nephritis
HP:0000124	Renal tubular dysfunction
HP:0000125	Pelvic kidney
HP:0000126	Hydronephrosis
HP:0000127	Renal salt wasting
HP:0000128	Renal potassium wasting
HP:0000130	Abnormality of the uterus
HP:0000131	Uterine leiomyoma
HP:0000132	Menorrhagia
HP:0000133	Gonadal dysgenesis
HP:0000134	Female hypogonadism
HP:0000135	Hypogonadism
HP:0000136	Bifid uterus
HP:0000137	Abnormality of the ovary
HP:0000138	Ovarian cyst
HP:0000139	Uterine prolapse
HP:0000140	Abnormality of the menstrual cycle
HP:0000141	Amenorrhea
HP:0000142	Abnormal vagina morphology
HP:0000143	Rectovaginal fistula
HP:0000144	Decreased fertility
HP:0000145	Transverse vaginal septum
HP:0000147	Polycystic ovaries
HP:0000148	Vaginal atresia
HP:0000149	Ovarian gonadoblastoma
HP:0000150	Gonadoblastoma
HP:0000151	Aplasia of the uterus
HP:0000152	Abnormality of head or neck
HP:0000153	Abnormality of the mouth
HP:0000154	Wide mouth
HP:0000155	Oral ulcer
HP:0000157	Abnormality of the tongue
HP:0000158	Macroglossia
HP:0000159	Abnormal lip morphology
HP:0000160	Narrow mouth
HP:0000161	Median cleft lip
HP:0000162	Glossoptosis
HP:0000163	Abnormal oral cavity morphology
HP:0000164	Abnormality of the dentition
HP:0000166	Severe periodontitis
HP:0000168	Abnormality of the gingiva
HP:0000169	Gingival fibromatosis
HP:0000171	Microglossia
HP:0000172	Abnormality of the uvula
HP:0000174	Abnormal palate morphology
HP:0000175	Cleft palate
HP:0000176	Submucous cleft hard palate
HP:0000177	Abnormality of upper lip
HP:0000178	Abnormality of lower lip
HP:0000179	Thick lower lip vermilion
HP:0000180	Lobulated tongue
HP:0000182	Movement abnormality of the tongue
HP:0000183	Difficulty in tongue movements
HP:0000185	Cleft soft palate
HP:0000187	Broad alveolar ridges
HP:0000188	Short upper lip
HP:0000189	Narrow palate
HP:0000190	Abnormal oral frenulum morphology
HP:0000191	Accessory oral frenulum
HP:0000193	Bifid uvula
HP:0000194	Open mouth
HP:0000196	Lower lip pit
HP:0000197	Abnormal parotid gland morphology
HP:0000198	Absence of Stensen duct
HP:0000199	Tongue nodules
HP:0000200	Short lingual frenulum
HP:0000201	Pierre-Robin sequence
HP:0000202	Oral cleft
HP:0000204	Cleft upper lip
HP:0000205	Pursed lips
HP:0000206	Glossitis
HP:0000207	Triangular mouth
HP:0000211	Trismus
HP:0000212	Gingival overgrowth
HP:0000214	Lip telangiectasia
HP:0000215	Thick upper lip vermilion
HP:0000216	Broad secondary alveolar ridge
HP:0000217	Xerostomia
HP:0000218	High palate
HP:0000219	Thin upper lip vermilion
HP:0000220	Velopharyngeal insufficiency
HP:0000221	Furrowed tongue
HP:0000222	Gingival hyperkeratosis
HP:0000223	Abnormality of taste sensation
HP:0000224	Decreased taste sensation
HP:0000225	Gingival bleeding
HP:0000227	Tongue telangiectasia
HP:0000228	Oral cavity telangiectasia
HP:0000230	Gingivitis
HP:0000232	Everted lower lip vermilion
HP:0000233	Thin vermilion border
HP:0000234	Abnormality of the head
HP:0000235	Abnormality of the fontanelles or cranial sutures
HP:0000236	Abnormality of the anterior fontanelle
HP:0000237	Small anterior fontanelle
HP:0000238	Hydrocephalus
HP:0000239	Large fontanelles
HP:0000240	Abnormality of skull size
HP:0000242	Parietal bossing
HP:0000243	Trigonocephaly
HP:0000244	Brachyturricephaly
HP:0000245	Abnormality of the paranasal sinuses
HP:0000246	Sinusitis
HP:0000248	Brachycephaly
HP:0000250	Dense calvaria
HP:0000252	Microcephaly
HP:0000253	Progressive microcephaly
HP:0000255	Acute sinusitis
HP:0000256	Macrocephaly
HP:0000260	Wide anterior fontanel
HP:0000262	Turricephaly
HP:0000263	Oxycephaly
HP:0000264	Abnormality of the mastoid
HP:0000265	Mastoiditis
HP:0000267	Cranial asymmetry
HP:0000268	Dolichocephaly
HP:0000269	Prominent occiput
HP:0000270	Delayed cranial suture closure
HP:0000271	Abnormality of the face
HP:0000272	Malar flattening
HP:0000273	Facial grimacing
HP:0000274	Small face
HP:0000275	Narrow face
HP:0000276	Long face
HP:0000277	Abnormality of the mandible
HP:0000278	Retrognathia
HP:0000280	Coarse facial features
HP:0000282	Facial edema
HP:0000283	Broad face
HP:0000284	obsolete Abnormality of the ocular region
HP:0000286	Epicanthus
HP:0000287	Increased facial adipose tissue
HP:0000288	Abnormality of the philtrum
HP:0000289	Broad philtrum
HP:0000290	Abnormality of the forehead
HP:0000291	Abnormality of facial adipose tissue
HP:0000292	Loss of facial adipose tissue
HP:0000293	Full cheeks
HP:0000294	Low anterior hairline
HP:0000295	Doll-like facies
HP:0000297	Facial hypotonia
HP:0000298	Mask-like facies
HP:0000300	Oval face
HP:0000301	Abnormality of facial musculature
HP:0000303	Mandibular prognathia
HP:0000306	Abnormality of the chin
HP:0000307	Pointed chin
HP:0000308	Microretrognathia
HP:0000309	Abnormality of the midface
HP:0000311	Round face
HP:0000315	Abnormality of the orbital region
HP:0000316	Hypertelorism
HP:0000317	Facial myokymia
HP:0000319	Smooth philtrum
HP:0000320	Bird-like facies
HP:0000321	Square face
HP:0000322	Short philtrum
HP:0000324	Facial asymmetry
HP:0000325	Triangular face
HP:0000326	Abnormality of the maxilla
HP:0000327	Hypoplasia of the maxilla
HP:0000329	Facial hemangioma
HP:0000331	Short chin
HP:0000336	Prominent supraorbital ridges
HP:0000337	Broad forehead
HP:0000338	Hypomimic face
HP:0000339	Pugilistic facies
HP:0000340	Sloping forehead
HP:0000341	Narrow forehead
HP:0000343	Long philtrum
HP:0000346	Whistling appearance
HP:0000347	Micrognathia
HP:0000348	High forehead
HP:0000349	Widow's peak
HP:0000350	Small forehead
HP:0000356	Abnormality of the outer ear
HP:0000357	Abnormal location of ears
HP:0000358	Posteriorly rotated ears
HP:0000359	Abnormality of the inner ear
HP:0000360	Tinnitus
HP:0000361	obsolete Pulsatile tinnitus (tympanic paraganglioma)
HP:0000362	Otosclerosis
HP:0000363	Abnormality of earlobe
HP:0000364	Hearing abnormality
HP:0000365	Hearing impairment
HP:0000366	Abnormality of the nose
HP:0000368	Low-set, posteriorly rotated ears
HP:0000369	Low-set ears
HP:0000370	Abnormality of the middle ear
HP:0000371	Acute otitis media
HP:0000372	Abnormality of the auditory canal
HP:0000375	Abnormal cochlea morphology
HP:0000376	Incomplete partition of the cochlea type II
HP:0000377	Abnormality of the pinna
HP:0000378	Cupped ear
HP:0000381	Stapes ankylosis
HP:0000383	Abnormality of periauricular region
HP:0000384	Preauricular skin tag
HP:0000385	Small earlobe
HP:0000387	Absent earlobe
HP:0000388	Otitis media
HP:0000389	Chronic otitis media
HP:0000391	Thickened helices
HP:0000394	Lop ear
HP:0000395	Prominent antihelix
HP:0000396	Overfolded helix
HP:0000399	Prelingual sensorineural hearing impairment
HP:0000400	Macrotia
HP:0000402	Stenosis of the external auditory canal
HP:0000403	Recurrent otitis media
HP:0000405	Conductive hearing impairment
HP:0000407	Sensorineural hearing impairment
HP:0000408	Progressive sensorineural hearing impairment
HP:0000410	Mixed hearing impairment
HP:0000411	Protruding ear
HP:0000413	Atresia of the external auditory canal
HP:0000414	Bulbous nose
HP:0000415	Abnormality of the choanae
HP:0000417	Slender nose
HP:0000418	Narrow nasal ridge
HP:0000419	Abnormality of the nasal septum
HP:0000420	Short nasal septum
HP:0000421	Epistaxis
HP:0000422	Abnormality of the nasal bridge
HP:0000426	Prominent nasal bridge
HP:0000429	Abnormality of the nasal alae
HP:0000430	Underdeveloped nasal alae
HP:0000431	Wide nasal bridge
HP:0000433	Abnormality of the nasal mucosa
HP:0000434	Nasal mucosa telangiectasia
HP:0000436	Abnormality of the nasal tip
HP:0000437	Depressed nasal tip
HP:0000444	Convex nasal ridge
HP:0000445	Wide nose
HP:0000446	Narrow nasal bridge
HP:0000447	Pear-shaped nose
HP:0000448	Prominent nose
HP:0000451	Triangular nasal tip
HP:0000452	Choanal stenosis
HP:0000453	Choanal atresia
HP:0000454	Flared nostrils
HP:0000455	Broad nasal tip
HP:0000456	Bifid nasal tip
HP:0000457	Depressed nasal ridge
HP:0000458	Anosmia
HP:0000460	Narrow nose
HP:0000463	Anteverted nares
HP:0000464	Abnormality of the neck
HP:0000465	Webbed neck
HP:0000466	Limited neck range of motion
HP:0000467	Neck muscle weakness
HP:0000468	Increased adipose tissue around the neck
HP:0000470	Short neck
HP:0000471	Gastrointestinal angiodysplasia
HP:0000472	Long neck
HP:0000473	Torticollis
HP:0000474	Thickened nuchal skin fold
HP:0000475	Broad neck
HP:0000476	Cystic hygroma
HP:0000478	Abnormality of the eye
HP:0000479	Abnormal retinal morphology
HP:0000480	Retinal coloboma
HP:0000481	Abnormal cornea morphology
HP:0000482	Microcornea
HP:0000483	Astigmatism
HP:0000484	Hyperopic astigmatism
HP:0000485	Megalocornea
HP:0000486	Strabismus
HP:0000487	obsolete Congenital strabismus
HP:0000488	Retinopathy
HP:0000489	obsolete Abnormality of globe location or size
HP:0000490	Deeply set eye
HP:0000491	Keratitis
HP:0000492	Abnormal eyelid morphology
HP:0000493	Abnormal foveal morphology
HP:0000494	Downslanted palpebral fissures
HP:0000495	Recurrent corneal erosions
HP:0000496	Abnormality of eye movement
HP:0000497	Globe retraction and deviation on abduction
HP:0000498	Blepharitis
HP:0000499	Abnormal eyelash morphology
HP:0000501	Glaucoma
HP:0000502	Abnormal conjunctiva morphology
HP:0000503	Tortuosity of conjunctival vessels
HP:0000504	Abnormality of vision
HP:0000505	Visual impairment
HP:0000506	Telecanthus
HP:0000508	Ptosis
HP:0000509	Conjunctivitis
HP:0000510	Rod-cone dystrophy
HP:0000511	Vertical supranuclear gaze palsy
HP:0000512	Abnormal electroretinogram
HP:0000514	Slow saccadic eye movements
HP:0000517	Abnormality of the lens
HP:0000518	Cataract
HP:0000519	Developmental cataract
HP:0000520	Proptosis
HP:0000522	Alacrima
HP:0000523	Subcapsular cataract
HP:0000524	Conjunctival telangiectasia
HP:0000525	Abnormality iris morphology
HP:0000526	Aniridia
HP:0000527	Long eyelashes
HP:0000528	Anophthalmia
HP:0000529	Progressive visual loss
HP:0000531	Corneal crystals
HP:0000532	Abnormal chorioretinal morphology
HP:0000533	Chorioretinal atrophy
HP:0000534	Abnormal eyebrow morphology
HP:0000535	Sparse and thin eyebrow
HP:0000537	Epicanthus inversus
HP:0000538	Pseudopapilledema
HP:0000539	Abnormality of refraction
HP:0000540	Hypermetropia
HP:0000541	Retinal detachment
HP:0000542	Impaired ocular adduction
HP:0000543	Optic disc pallor
HP:0000544	External ophthalmoplegia
HP:0000545	Myopia
HP:0000546	Retinal degeneration
HP:0000547	obsolete Tapetoretinal degeneration
HP:0000548	Cone/cone-rod dystrophy
HP:0000549	Abnormal conjugate eye movement
HP:0000550	Undetectable electroretinogram
HP:0000551	Abnormality of color vision
HP:0000552	Tritanomaly
HP:0000553	Abnormal uvea morphology
HP:0000554	Uveitis
HP:0000555	Leukocoria
HP:0000556	Retinal dystrophy
HP:0000557	Buphthalmos
HP:0000558	Rieger anomaly
HP:0000559	Corneal scarring
HP:0000561	Absent eyelashes
HP:0000563	Keratoconus
HP:0000564	Lacrimal duct atresia
HP:0000565	Esotropia
HP:0000567	Chorioretinal coloboma
HP:0000568	Microphthalmia
HP:0000570	Abnormal saccadic eye movements
HP:0000571	Hypometric saccades
HP:0000572	Visual loss
HP:0000573	Retinal hemorrhage
HP:0000574	Thick eyebrow
HP:0000575	Scotoma
HP:0000576	Centrocecal scotoma
HP:0000577	Exotropia
HP:0000579	Nasolacrimal duct obstruction
HP:0000580	Pigmentary retinopathy
HP:0000581	Blepharophimosis
HP:0000582	Upslanted palpebral fissure
HP:0000584	Punctate corneal epithelial erosions
HP:0000585	Band keratopathy
HP:0000586	Shallow orbits
HP:0000587	Abnormality of the optic nerve
HP:0000588	Optic nerve coloboma
HP:0000589	Coloboma
HP:0000590	Progressive external ophthalmoplegia
HP:0000591	Abnormal sclera morphology
HP:0000592	Blue sclerae
HP:0000593	Abnormal anterior chamber morphology
HP:0000594	Shallow anterior chamber
HP:0000597	Ophthalmoparesis
HP:0000598	Abnormality of the ear
HP:0000599	Abnormality of the frontal hairline
HP:0000600	Abnormality of the pharynx
HP:0000601	Hypotelorism
HP:0000602	Ophthalmoplegia
HP:0000603	Central scotoma
HP:0000605	Supranuclear gaze palsy
HP:0000606	Abnormality of the periorbital region
HP:0000607	Periorbital wrinkles
HP:0000608	Macular degeneration
HP:0000609	Optic nerve hypoplasia
HP:0000610	Abnormal choroid morphology
HP:0000611	obsolete Choroid coloboma
HP:0000612	Iris coloboma
HP:0000613	Photophobia
HP:0000614	Abnormal nasolacrimal system morphology
HP:0000615	Abnormal pupil morphology
HP:0000616	Miosis
HP:0000617	Abnormality of ocular smooth pursuit
HP:0000618	Blindness
HP:0000619	Impaired convergence
HP:0000620	Dacryocystitis
HP:0000621	Entropion
HP:0000622	Blurred vision
HP:0000623	Supranuclear ophthalmoplegia
HP:0000625	Eyelid coloboma
HP:0000627	Posterior embryotoxon
HP:0000629	Periorbital fullness
HP:0000630	Abnormal retinal artery morphology
HP:0000631	Retinal arterial tortuosity
HP:0000632	Lacrimation abnormality
HP:0000633	Decreased lacrimation
HP:0000634	Impaired ocular abduction
HP:0000635	Blue irides
HP:0000636	Upper eyelid coloboma
HP:0000637	Long palpebral fissure
HP:0000639	Nystagmus
HP:0000640	Gaze-evoked nystagmus
HP:0000641	Dysmetric saccades
HP:0000642	Red-green dyschromatopsia
HP:0000643	Blepharospasm
HP:0000646	Amblyopia
HP:0000647	Sclerocornea
HP:0000648	Optic atrophy
HP:0000649	Abnormality of visual evoked potentials
HP:0000650	Abnormal amplitude of pattern reversal visual evoked potentials
HP:0000651	Diplopia
HP:0000652	Lower eyelid coloboma
HP:0000653	Sparse eyelashes
HP:0000654	Decreased light- and dark-adapted electroretinogram amplitude
HP:0000655	obsolete Vitreoretinal degeneration
HP:0000656	Ectropion
HP:0000657	Oculomotor apraxia
HP:0000658	Eyelid apraxia
HP:0000659	Peters anomaly
HP:0000660	Lipemia retinalis
HP:0000661	Palpebral fissure narrowing on adduction
HP:0000662	Nyctalopia
HP:0000664	Synophrys
HP:0000666	Horizontal nystagmus
HP:0000667	Phthisis bulbi
HP:0000668	Hypodontia
HP:0000670	Carious teeth
HP:0000674	Anodontia
HP:0000675	Macrodontia of permanent maxillary central incisor
HP:0000676	Abnormality of the incisor
HP:0000677	Oligodontia
HP:0000678	Dental crowding
HP:0000679	Taurodontia
HP:0000680	Delayed eruption of primary teeth
HP:0000682	Abnormality of dental enamel
HP:0000683	Grayish enamel
HP:0000684	Delayed eruption of teeth
HP:0000685	Hypoplasia of teeth
HP:0000687	Widely spaced teeth
HP:0000689	Dental malocclusion
HP:0000690	Agenesis of maxillary lateral incisor
HP:0000691	Microdontia
HP:0000692	Misalignment of teeth
HP:0000694	Shell teeth
HP:0000695	Natal tooth
HP:0000696	Delayed eruption of permanent teeth
HP:0000698	Conical tooth
HP:0000699	Diastema
HP:0000700	Periapical bone loss
HP:0000703	Dentinogenesis imperfecta
HP:0000704	Periodontitis
HP:0000705	Amelogenesis imperfecta
HP:0000706	Unerupted tooth
HP:0000707	Abnormality of the nervous system
HP:0000708	Behavioral abnormality
HP:0000709	Psychosis
HP:0000710	Hyperorality
HP:0000711	Restlessness
HP:0000712	Emotional lability
HP:0000713	Agitation
HP:0000716	Depressivity
HP:0000717	Autism
HP:0000718	Aggressive behavior
HP:0000719	Inappropriate behavior
HP:0000720	Mood swings
HP:0000721	Lack of spontaneous play
HP:0000722	Obsessive-compulsive behavior
HP:0000723	Restrictive behavior
HP:0000725	Psychotic episodes
HP:0000726	Dementia
HP:0000727	Frontal lobe dementia
HP:0000728	Impaired ability to form peer relationships
HP:0000729	Autistic behavior
HP:0000732	Inflexible adherence to routines or rituals
HP:0000733	Stereotypy
HP:0000734	Disinhibition
HP:0000735	Impaired social interactions
HP:0000736	Short attention span
HP:0000737	Irritability
HP:0000738	Hallucinations
HP:0000739	Anxiety
HP:0000740	Episodic paroxysmal anxiety
HP:0000741	Apathy
HP:0000742	Self-mutilation
HP:0000743	Frontal release signs
HP:0000744	Low frustration tolerance
HP:0000745	Diminished motivation
HP:0000746	Delusions
HP:0000748	Inappropriate laughter
HP:0000749	Paroxysmal bursts of laughter
HP:0000750	Delayed speech and language development
HP:0000751	Personality changes
HP:0000752	Hyperactivity
HP:0000753	Autism with high cognitive abilities
HP:0000756	Agoraphobia
HP:0000757	Lack of insight
HP:0000758	Impaired use of nonverbal behaviors
HP:0000759	Abnormal peripheral nervous system morphology
HP:0000762	Decreased nerve conduction velocity
HP:0000763	Sensory neuropathy
HP:0000764	Peripheral axonal degeneration
HP:0000765	Abnormality of the thorax
HP:0000766	Abnormality of the sternum
HP:0000767	Pectus excavatum
HP:0000768	Pectus carinatum
HP:0000769	Abnormality of the breast
HP:0000771	Gynecomastia
HP:0000772	Abnormality of the ribs
HP:0000773	Short ribs
HP:0000774	Narrow chest
HP:0000775	Abnormality of the diaphragm
HP:0000776	Congenital diaphragmatic hernia
HP:0000777	Abnormality of the thymus
HP:0000778	Hypoplasia of the thymus
HP:0000782	Abnormality of the scapula
HP:0000786	Primary amenorrhea
HP:0000787	Nephrolithiasis
HP:0000789	Infertility
HP:0000790	Hematuria
HP:0000791	Uric acid nephrolithiasis
HP:0000793	Membranoproliferative glomerulonephritis
HP:0000794	IgA deposition in the glomerulus
HP:0000795	Abnormality of the urethra
HP:0000796	Urethral obstruction
HP:0000798	Oligospermia
HP:0000799	Renal steatosis
HP:0000800	Cystic renal dysplasia
HP:0000802	Impotence
HP:0000803	Renal cortical cysts
HP:0000804	Xanthine nephrolithiasis
HP:0000805	Enuresis
HP:0000807	Glandular hypospadias
HP:0000808	Penoscrotal hypospadias
HP:0000809	Urinary tract atresia
HP:0000811	Abnormal external genitalia
HP:0000812	Abnormal internal genitalia
HP:0000813	Bicornuate uterus
HP:0000815	Hypergonadotropic hypogonadism
HP:0000816	Abnormality of Krebs cycle metabolism
HP:0000817	Poor eye contact
HP:0000818	Abnormality of the endocrine system
HP:0000819	Diabetes mellitus
HP:0000820	Abnormality of the thyroid gland
HP:0000821	Hypothyroidism
HP:0000822	Hypertension
HP:0000823	Delayed puberty
HP:0000824	Growth hormone deficiency
HP:0000825	Hyperinsulinemic hypoglycemia
HP:0000826	Precocious puberty
HP:0000828	Abnormality of the parathyroid gland
HP:0000829	Hypoparathyroidism
HP:0000830	Anterior hypopituitarism
HP:0000831	Insulin-resistant diabetes mellitus
HP:0000832	Primary hypothyroidism
HP:0000833	Glucose intolerance
HP:0000834	Abnormality of the adrenal glands
HP:0000835	Adrenal hypoplasia
HP:0000836	Hyperthyroidism
HP:0000837	Increased circulating gonadotropin level
HP:0000839	Pituitary dwarfism
HP:0000840	Adrenogenital syndrome
HP:0000841	Hyperactive renin-angiotensin system
HP:0000842	Hyperinsulinemia
HP:0000843	Hyperparathyroidism
HP:0000845	Growth hormone excess
HP:0000846	Adrenal insufficiency
HP:0000847	Abnormality of renin-angiotensin system
HP:0000848	Increased circulating renin level
HP:0000849	Adrenocortical abnormality
HP:0000851	Congenital hypothyroidism
HP:0000852	Pseudohypoparathyroidism
HP:0000853	Goiter
HP:0000854	Thyroid adenoma
HP:0000855	Insulin resistance
HP:0000857	Neonatal insulin-dependent diabetes mellitus
HP:0000858	Menstrual irregularities
HP:0000859	Hyperaldosteronism
HP:0000860	Parathyroid hypoplasia
HP:0000863	Central diabetes insipidus
HP:0000864	Abnormality of the hypothalamus-pituitary axis
HP:0000866	Euthyroid multinodular goiter
HP:0000867	Secondary hyperparathyroidism
HP:0000868	Decreased fertility in females
HP:0000869	Secondary amenorrhea
HP:0000870	Prolactin excess
HP:0000871	Panhypopituitarism
HP:0000872	Hashimoto thyroiditis
HP:0000873	Diabetes insipidus
HP:0000875	Episodic hypertension
HP:0000876	Oligomenorrhea
HP:0000877	Insulin-resistant diabetes mellitus at puberty
HP:0000878	11 pairs of ribs
HP:0000879	Short sternum
HP:0000882	Hypoplastic scapulae
HP:0000883	Thin ribs
HP:0000884	Prominent sternum
HP:0000885	Broad ribs
HP:0000886	Deformed rib cage
HP:0000887	Cupped ribs
HP:0000888	Horizontal ribs
HP:0000889	Abnormality of the clavicle
HP:0000890	Long clavicles
HP:0000891	Cervical ribs
HP:0000892	Bifid ribs
HP:0000893	Bulging of the costochondral junction
HP:0000894	Short clavicles
HP:0000895	Lateral clavicle hook
HP:0000896	Rib exostoses
HP:0000897	Rachitic rosary
HP:0000900	Thickened ribs
HP:0000902	Rib fusion
HP:0000904	Flaring of rib cage
HP:0000905	Progressive clavicular acroosteolysis
HP:0000907	Anterior rib cupping
HP:0000910	Wide-cupped costochondral junctions
HP:0000911	Flat glenoid fossa
HP:0000912	Sprengel anomaly
HP:0000913	Posterior rib fusion
HP:0000914	Shield chest
HP:0000915	Pectus excavatum of inferior sternum
HP:0000916	Broad clavicles
HP:0000917	Superior pectus carinatum
HP:0000918	Scapular exostoses
HP:0000919	Abnormality of the costochondral junction
HP:0000920	Enlargement of the costochondral junction
HP:0000921	Missing ribs
HP:0000922	Posterior rib cupping
HP:0000923	Beaded ribs
HP:0000924	Abnormality of the skeletal system
HP:0000925	Abnormality of the vertebral column
HP:0000926	Platyspondyly
HP:0000927	Abnormality of skeletal maturation
HP:0000929	Abnormality of the skull
HP:0000930	Elevated imprint of the transverse sinuses
HP:0000931	Thinning and bulging of the posterior fossa bones
HP:0000932	Abnormality of the posterior cranial fossa
HP:0000933	Posterior fossa cyst at the fourth ventricle
HP:0000934	Chondrocalcinosis
HP:0000935	Thickened cortex of long bones
HP:0000938	Osteopenia
HP:0000939	Osteoporosis
HP:0000940	Abnormal diaphysis morphology
HP:0000941	Short diaphyses
HP:0000943	Dysostosis multiplex
HP:0000944	Abnormality of the metaphysis
HP:0000946	Hypoplastic ilia
HP:0000947	Dumbbell-shaped long bone
HP:0000951	Abnormality of the skin
HP:0000952	Jaundice
HP:0000953	Hyperpigmentation of the skin
HP:0000954	Single transverse palmar crease
HP:0000956	Acanthosis nigricans
HP:0000957	Cafe-au-lait spot
HP:0000958	Dry skin
HP:0000960	Sacral dimple
HP:0000961	Cyanosis
HP:0000962	Hyperkeratosis
HP:0000963	Thin skin
HP:0000964	Eczema
HP:0000965	Cutis marmorata
HP:0000966	Hypohidrosis
HP:0000967	Petechiae
HP:0000968	Ectodermal dysplasia
HP:0000969	Edema
HP:0000970	Anhidrosis
HP:0000971	Abnormality of the sweat gland
HP:0000972	Palmoplantar hyperkeratosis
HP:0000973	Cutis laxa
HP:0000974	Hyperextensible skin
HP:0000975	Hyperhidrosis
HP:0000976	Eczematoid dermatitis
HP:0000977	Soft skin
HP:0000978	Bruising susceptibility
HP:0000979	Purpura
HP:0000980	Pallor
HP:0000982	Palmoplantar keratoderma
HP:0000987	Atypical scarring of skin
HP:0000988	Skin rash
HP:0000989	Pruritus
HP:0000991	Xanthomatosis
HP:0000992	Cutaneous photosensitivity
HP:0000993	Molluscoid pseudotumors
HP:0000995	Melanocytic nevus
HP:0000996	Facial capillary hemangioma
HP:0000997	Axillary freckling
HP:0000998	Hypertrichosis
HP:0000999	Pyoderma
HP:0001000	Abnormality of skin pigmentation
HP:0001001	Abnormality of subcutaneous fat tissue
HP:0001002	obsolete Decreased subcutaneous fat
HP:0001003	Multiple lentigines
HP:0001004	Lymphedema
HP:0001005	Dermatological manifestations of systemic disorders
HP:0001006	Hypotrichosis
HP:0001007	Hirsutism
HP:0001008	Accumulation of melanosomes in melanocytes
HP:0001009	Telangiectasia
HP:0001010	Hypopigmentation of the skin
HP:0001011	obsolete Diaphoresis (with pheochromocytoma)
HP:0001012	Multiple lipomas
HP:0001013	Eruptive xanthomas
HP:0001014	Angiokeratoma
HP:0001015	Prominent superficial veins
HP:0001017	Anemic pallor
HP:0001018	Abnormal palmar dermatoglyphics
HP:0001019	Erythroderma
HP:0001022	Albinism
HP:0001024	Skin dimple over apex of long bone angulation
HP:0001025	Urticaria
HP:0001026	Penetrating foot ulcers
HP:0001027	Soft, doughy skin
HP:0001028	Hemangioma
HP:0001029	Poikiloderma
HP:0001030	Fragile skin
HP:0001031	Subcutaneous lipoma
HP:0001032	Absent distal interphalangeal creases
HP:0001033	Facial flushing after alcohol intake
HP:0001034	Hypermelanotic macule
HP:0001036	Parakeratosis
HP:0001038	Warfarin-induced skin necrosis
HP:0001039	Atheroeruptive xanthoma
HP:0001040	Multiple pterygia
HP:0001041	Facial erythema
HP:0001042	High axial triradius
HP:0001043	Prominent scalp veins
HP:0001045	Vitiligo
HP:0001046	Intermittent jaundice
HP:0001047	Atopic dermatitis
HP:0001048	Cavernous hemangioma
HP:0001049	Absent dorsal skin creases over affected joints
HP:0001050	Plethora
HP:0001051	Seborrheic dermatitis
HP:0001052	Nevus flammeus
HP:0001053	Hypopigmented skin patches
HP:0001054	Numerous nevi
HP:0001055	Erysipelas
HP:0001056	Milia
HP:0001057	Aplasia cutis congenita
HP:0001058	Poor wound healing
HP:0001059	Pterygium
HP:0001060	Axillary pterygium
HP:0001061	Acne
HP:0001062	Atypical nevus
HP:0001063	Acrocyanosis
HP:0001065	Striae distensae
HP:0001067	Neurofibromas
HP:0001069	Episodic hyperhidrosis
HP:0001070	Mottled pigmentation
HP:0001071	Angiokeratoma corporis diffusum
HP:0001072	Thickened skin
HP:0001073	Cigarette-paper scars
HP:0001074	Atypical nevi in non-sun exposed areas
HP:0001075	Atrophic scars
HP:0001076	Glabellar hemangioma
HP:0001080	Biliary tract abnormality
HP:0001081	Cholelithiasis
HP:0001082	Cholecystitis
HP:0001083	Ectopia lentis
HP:0001084	Corneal arcus
HP:0001085	Papilledema
HP:0001087	Developmental glaucoma
HP:0001088	Brushfield spots
HP:0001089	Iris atrophy
HP:0001090	Abnormally large globe
HP:0001092	Absent lacrimal punctum
HP:0001093	Optic nerve dysplasia
HP:0001094	Iridocyclitis
HP:0001095	Hypertensive retinopathy
HP:0001096	Keratoconjunctivitis
HP:0001097	Keratoconjunctivitis sicca
HP:0001098	Abnormal fundus morphology
HP:0001099	Fundus atrophy
HP:0001100	Heterochromia iridis
HP:0001101	Iritis
HP:0001102	Angioid streaks of the fundus
HP:0001103	Abnormal macular morphology
HP:0001104	Macular hypoplasia
HP:0001105	Retinal atrophy
HP:0001106	Periorbital hyperpigmentation
HP:0001107	Ocular albinism
HP:0001112	Leber optic atrophy
HP:0001113	obsolete Early cataracts
HP:0001114	Xanthelasma
HP:0001115	Posterior polar cataract
HP:0001116	Macular coloboma
HP:0001117	Sudden loss of visual acuity
HP:0001118	Juvenile cataract
HP:0001119	Keratoglobus
HP:0001120	Abnormality of corneal size
HP:0001122	obsolete Aplasia/Hypoplasia of the choroid
HP:0001123	Visual field defect
HP:0001125	Transient unilateral blurring of vision
HP:0001126	Cryptophthalmos
HP:0001128	Trichiasis
HP:0001129	Large central visual field defect
HP:0001131	Corneal dystrophy
HP:0001132	Lens subluxation
HP:0001133	Constriction of peripheral visual field
HP:0001134	Anterior polar cataract
HP:0001135	Chorioretinal dystrophy
HP:0001136	Retinal arteriolar tortuosity
HP:0001137	Alternating esotropia
HP:0001138	Optic neuropathy
HP:0001139	Choroideremia
HP:0001140	Limbal dermoid
HP:0001141	Severely reduced visual acuity
HP:0001142	Lenticonus
HP:0001144	Orbital cyst
HP:0001145	obsolete Chorioretinopathy
HP:0001146	obsolete Pigmentary retinal degeneration
HP:0001147	Retinal exudate
HP:0001149	Lattice corneal dystrophy
HP:0001150	obsolete Choroidal sclerosis
HP:0001151	Impaired horizontal smooth pursuit
HP:0001152	Saccadic smooth pursuit
HP:0001153	Septate vagina
HP:0001155	Abnormality of the hand
HP:0001156	Brachydactyly
HP:0001159	Syndactyly
HP:0001161	Hand polydactyly
HP:0001162	Postaxial hand polydactyly
HP:0001163	Abnormality of the metacarpal bones
HP:0001166	Arachnodactyly
HP:0001167	Abnormality of finger
HP:0001169	Broad palm
HP:0001171	Split hand
HP:0001172	Abnormal thumb morphology
HP:0001176	Large hands
HP:0001177	Preaxial hand polydactyly
HP:0001178	Ulnar claw
HP:0001180	Hand oligodactyly
HP:0001181	Adducted thumb
HP:0001182	Tapered finger
HP:0001187	Hyperextensibility of the finger joints
HP:0001188	Hand clenching
HP:0001191	Abnormality of the carpal bones
HP:0001193	Ulnar deviation of the hand or of fingers of the hand
HP:0001194	Abnormalities of placenta or umbilical cord
HP:0001195	Single umbilical artery
HP:0001196	Short umbilical cord
HP:0001197	Abnormality of prenatal development or birth
HP:0001199	Triphalangeal thumb
HP:0001204	Distal symphalangism of hands
HP:0001211	Abnormal fingertip morphology
HP:0001212	Prominent fingertip pads
HP:0001215	Camptodactyly of 2nd-5th fingers
HP:0001216	Delayed ossification of carpal bones
HP:0001217	Clubbing
HP:0001218	Autoamputation
HP:0001220	Interphalangeal joint contracture of finger
HP:0001222	Spatulate thumbs
HP:0001223	Pointed proximal second through fifth metacarpals
HP:0001225	Wrist swelling
HP:0001226	obsolete Acral ulceration and osteomyelitis leading to autoamputation of digits
HP:0001227	Abnormality of the thenar eminence
HP:0001230	Broad metacarpals
HP:0001231	Abnormality of the fingernails
HP:0001232	Nail bed telangiectasia
HP:0001233	2-3 finger syndactyly
HP:0001234	Hitchhiker thumb
HP:0001238	Slender finger
HP:0001239	Wrist flexion contracture
HP:0001241	Capitate-hamate fusion
HP:0001245	Small thenar eminence
HP:0001248	Short tubular bones of the hand
HP:0001249	Intellectual disability
HP:0001250	Seizures
HP:0001251	Ataxia
HP:0001252	Muscular hypotonia
HP:0001254	Lethargy
HP:0001256	Intellectual disability, mild
HP:0001257	Spasticity
HP:0001258	Spastic paraplegia
HP:0001259	Coma
HP:0001260	Dysarthria
HP:0001262	Excessive daytime somnolence
HP:0001263	Global developmental delay
HP:0001264	Spastic diplegia
HP:0001265	Hyporeflexia
HP:0001266	Choreoathetosis
HP:0001268	Mental deterioration
HP:0001269	Hemiparesis
HP:0001270	Motor delay
HP:0001271	Polyneuropathy
HP:0001272	Cerebellar atrophy
HP:0001273	Abnormal corpus callosum morphology
HP:0001274	Agenesis of corpus callosum
HP:0001276	Hypertonia
HP:0001278	Orthostatic hypotension
HP:0001279	Syncope
HP:0001281	Tetany
HP:0001283	Bulbar palsy
HP:0001284	Areflexia
HP:0001285	Spastic tetraparesis
HP:0001287	Meningitis
HP:0001288	Gait disturbance
HP:0001289	Confusion
HP:0001290	Generalized hypotonia
HP:0001291	Abnormal cranial nerve morphology
HP:0001293	Cranial nerve compression
HP:0001297	Stroke
HP:0001298	Encephalopathy
HP:0001300	Parkinsonism
HP:0001301	Chronic sensorineural polyneuropathy
HP:0001302	Pachygyria
HP:0001304	Torsion dystonia
HP:0001305	Dandy-Walker malformation
HP:0001308	Tongue fasciculations
HP:0001310	Dysmetria
HP:0001311	Abnormal nervous system electrophysiology
HP:0001312	Giant somatosensory evoked potentials
HP:0001315	Reduced tendon reflexes
HP:0001317	Abnormal cerebellum morphology
HP:0001319	Neonatal hypotonia
HP:0001320	Cerebellar vermis hypoplasia
HP:0001321	Cerebellar hypoplasia
HP:0001322	Brain very small
HP:0001324	Muscle weakness
HP:0001325	Hypoglycemic coma
HP:0001326	EEG with irregular generalized spike and wave complexes
HP:0001327	Photomyoclonic seizures
HP:0001328	Specific learning disability
HP:0001331	Absent septum pellucidum
HP:0001332	Dystonia
HP:0001334	Communicating hydrocephalus
HP:0001335	Bimanual synkinesia
HP:0001336	Myoclonus
HP:0001337	Tremor
HP:0001338	Partial agenesis of the corpus callosum
HP:0001339	Lissencephaly
HP:0001340	Enhancement of the C-reflex
HP:0001341	Olfactory lobe agenesis
HP:0001342	Cerebral hemorrhage
HP:0001343	Kernicterus
HP:0001344	Absent speech
HP:0001345	Psychotic mentation
HP:0001347	Hyperreflexia
HP:0001348	Brisk reflexes
HP:0001349	Facial diplegia
HP:0001350	Slurred speech
HP:0001351	Jerk-locked premyoclonus spikes
HP:0001355	Megalencephaly
HP:0001357	Plagiocephaly
HP:0001360	Holoprosencephaly
HP:0001361	Nystagmus-induced head nodding
HP:0001362	Calvarial skull defect
HP:0001363	Craniosynostosis
HP:0001367	Abnormal joint morphology
HP:0001369	Arthritis
HP:0001370	Rheumatoid arthritis
HP:0001371	Flexion contracture
HP:0001373	Joint dislocation
HP:0001374	Congenital hip dislocation
HP:0001376	Limitation of joint mobility
HP:0001377	Limited elbow extension
HP:0001379	obsolete Degenerative joint disease
HP:0001380	obsolete Ligamentous laxity
HP:0001382	Joint hypermobility
HP:0001384	Abnormality of the hip joint
HP:0001385	Hip dysplasia
HP:0001386	Joint swelling
HP:0001387	Joint stiffness
HP:0001388	Joint laxity
HP:0001392	Abnormality of the liver
HP:0001394	Cirrhosis
HP:0001395	Hepatic fibrosis
HP:0001396	Cholestasis
HP:0001397	Hepatic steatosis
HP:0001399	Hepatic failure
HP:0001400	obsolete Hepatic abscesses due to immunodeficiency
HP:0001401	Intrahepatic biliary dysgenesis
HP:0001402	Hepatocellular carcinoma
HP:0001403	Macrovesicular hepatic steatosis
HP:0001404	Hepatocellular necrosis
HP:0001405	Periportal fibrosis
HP:0001406	Intrahepatic cholestasis
HP:0001407	Hepatic cysts
HP:0001408	Bile duct proliferation
HP:0001409	Portal hypertension
HP:0001410	Decreased liver function
HP:0001412	Enteroviral hepatitis
HP:0001413	Micronodular cirrhosis
HP:0001414	Microvesicular hepatic steatosis
HP:0001417	X-linked inheritance
HP:0001419	X-linked recessive inheritance
HP:0001421	Abnormality of the musculature of the hand
HP:0001423	X-linked dominant inheritance
HP:0001425	Heterogeneous
HP:0001426	Multifactorial inheritance
HP:0001427	Mitochondrial inheritance
HP:0001428	Somatic mutation
HP:0001430	Abnormality of the calf musculature
HP:0001433	Hepatosplenomegaly
HP:0001435	Abnormality of the shoulder girdle musculature
HP:0001436	Abnormality of the foot musculature
HP:0001437	Abnormality of the musculature of the lower limbs
HP:0001438	Abnormality of abdomen morphology
HP:0001440	Metatarsal synostosis
HP:0001441	Abnormality of the musculature of the thigh
HP:0001442	Somatic mosaicism
HP:0001443	Abnormality of the gluteal musculature
HP:0001444	Autosomal dominant somatic cell mutation
HP:0001445	Abnormality of the hip-girdle musculature
HP:0001446	Abnormality of the musculature of the upper limbs
HP:0001449	Duplication of metatarsal bones
HP:0001450	Y-linked inheritance
HP:0001452	Autosomal dominant contiguous gene syndrome
HP:0001454	Abnormality of the upper arm
HP:0001457	Abnormality of the musculature of the upper arm
HP:0001459	1-3 toe syndactyly
HP:0001460	Aplasia/Hypoplasia involving the skeletal musculature
HP:0001464	Aplasia/Hypoplasia involving the shoulder musculature
HP:0001465	Amyotrophy involving the shoulder musculature
HP:0001466	Contiguous gene syndrome
HP:0001467	Aplasia/Hypoplasia involving the musculature of the upper limbs
HP:0001468	Aplasia/Hypoplasia involving the musculature of the upper arm
HP:0001469	Abnormality of the musculature of the pelvis
HP:0001470	Sex-limited autosomal dominant
HP:0001471	Aplasia/Hypoplasia of the musculature of the pelvis
HP:0001472	obsolete Familial predisposition
HP:0001473	Metatarsal osteolysis
HP:0001474	Sclerotic scapulae
HP:0001475	Male-limited autosomal dominant
HP:0001476	Delayed closure of the anterior fontanelle
HP:0001477	Compensatory chin elevation
HP:0001480	Freckling
HP:0001482	Subcutaneous nodule
HP:0001483	Eye poking
HP:0001487	obsolete Hypopigmented fundi
HP:0001488	Bilateral ptosis
HP:0001489	Posterior vitreous detachment
HP:0001491	Congenital fibrosis of extraocular muscles
HP:0001492	Axenfeld anomaly
HP:0001493	Falciform retinal fold
HP:0001495	Carpal osteolysis
HP:0001498	Carpal bone hypoplasia
HP:0001500	Broad finger
HP:0001501	6 metacarpals
HP:0001504	Metacarpal osteolysis
HP:0001507	Growth abnormality
HP:0001508	Failure to thrive
HP:0001510	Growth delay
HP:0001511	Intrauterine growth retardation
HP:0001513	Obesity
HP:0001518	Small for gestational age
HP:0001519	Disproportionate tall stature
HP:0001520	Large for gestational age
HP:0001522	Death in infancy
HP:0001525	Severe failure to thrive
HP:0001528	Hemihypertrophy
HP:0001530	Mild postnatal growth retardation
HP:0001531	Failure to thrive in infancy
HP:0001533	Slender build
HP:0001537	Umbilical hernia
HP:0001538	Protuberant abdomen
HP:0001539	Omphalocele
HP:0001540	Diastasis recti
HP:0001541	Ascites
HP:0001543	Gastroschisis
HP:0001544	Prominent umbilicus
HP:0001545	Anteriorly placed anus
HP:0001547	Abnormality of the rib cage
HP:0001548	Overgrowth
HP:0001549	Abnormal ileum morphology
HP:0001551	Abnormality of the umbilicus
HP:0001552	Barrel-shaped chest
HP:0001555	Asymmetry of the thorax
HP:0001557	Prenatal movement abnormality
HP:0001558	Decreased fetal movement
HP:0001560	Abnormality of the amniotic fluid
HP:0001561	Polyhydramnios
HP:0001562	Oligohydramnios
HP:0001563	Fetal polyuria
HP:0001566	Widely-spaced maxillary central incisors
HP:0001571	Multiple impacted teeth
HP:0001572	Macrodontia
HP:0001574	Abnormality of the integument
HP:0001575	Mood changes
HP:0001579	Primary hypercortisolism
HP:0001580	Pigmented micronodular adrenocortical disease
HP:0001581	Recurrent skin infections
HP:0001582	Redundant skin
HP:0001583	Rotary nystagmus
HP:0001586	Vesicovaginal fistula
HP:0001587	obsolete Primary ovarian failure
HP:0001591	Bell-shaped thorax
HP:0001592	Selective tooth agenesis
HP:0001593	Maxillary lateral incisor microdontia
HP:0001595	Abnormality of the hair
HP:0001596	Alopecia
HP:0001597	Abnormality of the nail
HP:0001598	Concave nail
HP:0001600	Abnormality of the larynx
HP:0001601	Laryngomalacia
HP:0001602	Laryngeal stenosis
HP:0001604	Vocal cord paresis
HP:0001605	Vocal cord paralysis
HP:0001606	obsolete Vocal cord paralysis (caused by tumor impingement)
HP:0001607	Subglottic stenosis
HP:0001608	Abnormality of the voice
HP:0001609	Hoarse voice
HP:0001611	Nasal speech
HP:0001612	Weak cry
HP:0001613	obsolete Hoarse voice (caused by tumor impingement)
HP:0001615	Hoarse cry
HP:0001618	Dysphonia
HP:0001620	High pitched voice
HP:0001621	Weak voice
HP:0001622	Premature birth
HP:0001623	Breech presentation
HP:0001626	Abnormality of the cardiovascular system
HP:0001627	Abnormal heart morphology
HP:0001629	Ventricular septal defect
HP:0001631	Atrial septal defect
HP:0001633	Abnormal mitral valve morphology
HP:0001634	Mitral valve prolapse
HP:0001635	Congestive heart failure
HP:0001636	Tetralogy of Fallot
HP:0001637	Abnormal myocardium morphology
HP:0001638	Cardiomyopathy
HP:0001639	Hypertrophic cardiomyopathy
HP:0001640	Cardiomegaly
HP:0001641	Abnormal pulmonary valve morphology
HP:0001642	Pulmonic stenosis
HP:0001643	Patent ductus arteriosus
HP:0001644	Dilated cardiomyopathy
HP:0001645	Sudden cardiac death
HP:0001646	Abnormal aortic valve morphology
HP:0001647	Bicuspid aortic valve
HP:0001648	Cor pulmonale
HP:0001649	Tachycardia
HP:0001650	Aortic valve stenosis
HP:0001651	Dextrocardia
HP:0001653	Mitral regurgitation
HP:0001654	Abnormal heart valve morphology
HP:0001655	Patent foramen ovale
HP:0001657	Prolonged QT interval
HP:0001658	Myocardial infarction
HP:0001659	Aortic regurgitation
HP:0001660	Truncus arteriosus
HP:0001662	Bradycardia
HP:0001663	Ventricular fibrillation
HP:0001664	Torsade de pointes
HP:0001667	Right ventricular hypertrophy
HP:0001669	Transposition of the great arteries
HP:0001670	Asymmetric septal hypertrophy
HP:0001671	Abnormal cardiac septum morphology
HP:0001673	obsolete Tachycardia (with pheochromocytoma)
HP:0001674	Complete atrioventricular canal defect
HP:0001675	obsolete Rhythm disturbances associated with pheochromocytoma
HP:0001676	obsolete Palpitations (with pheochromocytoma)
HP:0001677	Coronary artery atherosclerosis
HP:0001678	Atrioventricular block
HP:0001679	Abnormal aortic morphology
HP:0001680	Coarctation of aorta
HP:0001681	Angina pectoris
HP:0001682	Subvalvular aortic stenosis
HP:0001683	Ectopia cordis
HP:0001684	Secundum atrial septal defect
HP:0001685	Myocardial fibrosis
HP:0001686	Loss of voice
HP:0001688	Sinus bradycardia
HP:0001691	Muscular subvalvular aortic stenosis
HP:0001692	Atrial arrhythmia
HP:0001693	Cardiac shunt
HP:0001694	Right-to-left shunt
HP:0001695	Cardiac arrest
HP:0001696	Situs inversus totalis
HP:0001697	Abnormal pericardium morphology
HP:0001698	Pericardial effusion
HP:0001699	Sudden death
HP:0001700	Myocardial necrosis
HP:0001701	Pericarditis
HP:0001702	Abnormal tricuspid valve morphology
HP:0001704	Tricuspid valve prolapse
HP:0001705	Right ventricular outlet tract obstruction
HP:0001706	Endocardial fibroelastosis
HP:0001707	Abnormal right ventricle morphology
HP:0001708	Right ventricular failure
HP:0001709	Third degree atrioventricular block
HP:0001710	Conotruncal defect
HP:0001711	Abnormal left ventricle morphology
HP:0001712	Left ventricular hypertrophy
HP:0001713	Abnormal cardiac ventricle morphology
HP:0001714	Ventricular hypertrophy
HP:0001716	Wolff-Parkinson-White syndrome
HP:0001717	Coronary artery calcification
HP:0001718	Mitral stenosis
HP:0001719	Double outlet right ventricle
HP:0001722	High-output congestive heart failure
HP:0001723	Restrictive cardiomyopathy
HP:0001724	obsolete Aortic dilatation
HP:0001726	obsolete Increased prevalence of valvular disease
HP:0001727	Thromboembolic stroke
HP:0001730	Progressive hearing impairment
HP:0001732	Abnormality of the pancreas
HP:0001733	Pancreatitis
HP:0001734	Annular pancreas
HP:0001735	Acute pancreatitis
HP:0001737	Pancreatic cysts
HP:0001738	Exocrine pancreatic insufficiency
HP:0001739	Abnormality of the nasopharynx
HP:0001741	Phimosis
HP:0001742	Nasal obstruction
HP:0001743	Abnormality of the spleen
HP:0001744	Splenomegaly
HP:0001746	Asplenia
HP:0001747	Accessory spleen
HP:0001748	Polysplenia
HP:0001750	Single ventricle
HP:0001751	Vestibular dysfunction
HP:0001756	Vestibular hypofunction
HP:0001757	High-frequency sensorineural hearing impairment
HP:0001760	Abnormality of the foot
HP:0001761	Pes cavus
HP:0001762	Talipes equinovarus
HP:0001763	Pes planus
HP:0001765	Hammertoe
HP:0001769	Broad foot
HP:0001770	Toe syndactyly
HP:0001771	Achilles tendon contracture
HP:0001772	Talipes equinovalgus
HP:0001773	Short foot
HP:0001775	Tarsal osteovalgus
HP:0001776	Bilateral talipes equinovarus
HP:0001780	Abnormality of toe
HP:0001782	Bulbous tips of toes
HP:0001783	Broad metatarsal
HP:0001785	Ankle swelling
HP:0001786	Narrow foot
HP:0001787	Abnormal delivery
HP:0001788	Premature rupture of membranes
HP:0001789	Hydrops fetalis
HP:0001790	Nonimmune hydrops fetalis
HP:0001791	Fetal ascites
HP:0001792	Small nail
HP:0001795	Hyperconvex nail
HP:0001798	Anonychia
HP:0001799	Short nail
HP:0001800	Hypoplastic toenails
HP:0001802	Absent toenail
HP:0001803	Nail pits
HP:0001804	Hypoplastic fingernail
HP:0001805	Thick nail
HP:0001806	Onycholysis
HP:0001807	Ridged nail
HP:0001808	Fragile nails
HP:0001809	Split nail
HP:0001810	Dystrophic toenail
HP:0001812	Hyperconvex fingernails
HP:0001814	Deep-set nails
HP:0001816	Thin nail
HP:0001817	Absent fingernail
HP:0001818	Paronychia
HP:0001820	Leukonychia
HP:0001821	Broad nail
HP:0001822	Hallux valgus
HP:0001824	Weight loss
HP:0001827	Genital tract atresia
HP:0001829	Foot polydactyly
HP:0001830	Postaxial foot polydactyly
HP:0001831	Short toe
HP:0001832	Abnormal metatarsal morphology
HP:0001833	Long foot
HP:0001836	Camptodactyly of toe
HP:0001837	Broad toe
HP:0001838	Rocker bottom foot
HP:0001839	Split foot
HP:0001840	Metatarsus adductus
HP:0001841	Preaxial foot polydactyly
HP:0001842	Foot acroosteolysis
HP:0001844	Abnormality of the hallux
HP:0001845	Overlapping toe
HP:0001847	Long hallux
HP:0001848	Calcaneovalgus deformity
HP:0001849	Foot oligodactyly
HP:0001850	Abnormality of the tarsal bones
HP:0001852	Sandal gap
HP:0001853	Bifid distal phalanx of toe
HP:0001854	Podagra
HP:0001857	Short distal phalanx of toe
HP:0001859	Distal foot symphalangism
HP:0001862	obsolete Acral ulceration and osteomyelitis leading to autoamputation of the digits (feet)
HP:0001863	Toe clinodactyly
HP:0001864	Clinodactyly of the 5th toe
HP:0001868	Autoamputation of foot
HP:0001869	Deep plantar creases
HP:0001870	Acroosteolysis of distal phalanges (feet)
HP:0001871	Abnormality of blood and blood-forming tissues
HP:0001872	Abnormal thrombocyte morphology
HP:0001873	Thrombocytopenia
HP:0001874	Abnormality of neutrophils
HP:0001875	Neutropenia
HP:0001876	Pancytopenia
HP:0001877	Abnormal erythrocyte morphology
HP:0001878	Hemolytic anemia
HP:0001879	Abnormal eosinophil morphology
HP:0001880	Eosinophilia
HP:0001881	Abnormal leukocyte morphology
HP:0001882	Leukopenia
HP:0001883	Talipes
HP:0001884	Talipes calcaneovalgus
HP:0001885	Short 2nd toe
HP:0001886	Foot osteomyelitis
HP:0001888	Lymphopenia
HP:0001889	Megaloblastic anemia
HP:0001890	Autoimmune hemolytic anemia
HP:0001891	Iron deficiency anemia
HP:0001892	Abnormal bleeding
HP:0001894	Thrombocytosis
HP:0001895	Normochromic anemia
HP:0001896	Reticulocytopenia
HP:0001897	Normocytic anemia
HP:0001898	Increased red blood cell mass
HP:0001899	Increased hematocrit
HP:0001900	Increased hemoglobin
HP:0001901	Polycythemia
HP:0001902	Giant platelets
HP:0001903	Anemia
HP:0001904	Neutropenia in presence of anti-neutropil antibodies
HP:0001905	Congenital thrombocytopenia
HP:0001907	Thromboembolism
HP:0001908	Hypoplastic anemia
HP:0001909	Leukemia
HP:0001911	Abnormal granulocyte morphology
HP:0001912	Abnormal basophil morphology
HP:0001913	Granulocytopenia
HP:0001915	Aplastic anemia
HP:0001917	Renal amyloidosis
HP:0001919	Acute kidney injury
HP:0001920	Renal artery stenosis
HP:0001922	Vacuolated lymphocytes
HP:0001923	Reticulocytosis
HP:0001924	Sideroblastic anemia
HP:0001927	Acanthocytosis
HP:0001928	Abnormality of coagulation
HP:0001929	Reduced factor XI activity
HP:0001930	Nonspherocytic hemolytic anemia
HP:0001931	Hypochromic anemia
HP:0001933	Subcutaneous hemorrhage
HP:0001934	Persistent bleeding after trauma
HP:0001935	Microcytic anemia
HP:0001937	Microangiopathic hemolytic anemia
HP:0001939	Abnormality of metabolism/homeostasis
HP:0001941	Acidosis
HP:0001942	Metabolic acidosis
HP:0001943	Hypoglycemia
HP:0001944	Dehydration
HP:0001945	Fever
HP:0001946	Ketosis
HP:0001947	Renal tubular acidosis
HP:0001948	Alkalosis
HP:0001949	Hypokalemic alkalosis
HP:0001950	Respiratory alkalosis
HP:0001951	Episodic ammonia intoxication
HP:0001952	Abnormal glucose tolerance
HP:0001953	Diabetic ketoacidosis
HP:0001954	Episodic fever
HP:0001955	Unexplained fevers
HP:0001956	Truncal obesity
HP:0001958	Nonketotic hypoglycemia
HP:0001959	Polydipsia
HP:0001960	Hypokalemic metabolic alkalosis
HP:0001961	Hypoplastic heart
HP:0001962	Palpitations
HP:0001963	Abnormal speech discrimination
HP:0001964	Aplasia/Hypoplasia of metatarsal bones
HP:0001965	Abnormality of the scalp
HP:0001966	Mesangial abnormality
HP:0001967	Diffuse mesangial sclerosis
HP:0001969	Tubulointerstitial abnormality
HP:0001970	Tubulointerstitial nephritis
HP:0001971	Hypersplenism
HP:0001972	Macrocytic anemia
HP:0001973	Autoimmune thrombocytopenia
HP:0001974	Leukocytosis
HP:0001975	Decreased platelet glycoprotein IIb-IIIa
HP:0001976	Reduced antithrombin III activity
HP:0001977	Abnormal thrombosis
HP:0001978	Extramedullary hematopoiesis
HP:0001980	Megaloblastic bone marrow
HP:0001981	Schistocytosis
HP:0001982	Sea-blue histiocytosis
HP:0001983	Reduced lymphocyte surface expression of CD43
HP:0001984	Intolerance to protein
HP:0001985	Hypoketotic hypoglycemia
HP:0001986	Hypertonic dehydration
HP:0001987	Hyperammonemia
HP:0001988	Recurrent hypoglycemia
HP:0001989	Fetal akinesia sequence
HP:0001991	Aplasia/Hypoplasia of toe
HP:0001992	Organic aciduria
HP:0001993	Ketoacidosis
HP:0001994	Renal Fanconi syndrome
HP:0001995	Hyperchloremic acidosis
HP:0001996	Chronic metabolic acidosis
HP:0001997	Gout
HP:0001998	Neonatal hypoglycemia
HP:0001999	Abnormal facial shape
HP:0002000	Short columella
HP:0002002	Deep philtrum
HP:0002003	Large forehead
HP:0002006	Facial cleft
HP:0002007	Frontal bossing
HP:0002009	Potter facies
HP:0002010	Narrow maxilla
HP:0002011	Morphological abnormality of the central nervous system
HP:0002012	Abnormality of the abdominal organs
HP:0002013	Vomiting
HP:0002014	Diarrhea
HP:0002015	Dysphagia
HP:0002017	Nausea and vomiting
HP:0002018	Nausea
HP:0002019	Constipation
HP:0002020	Gastroesophageal reflux
HP:0002021	Pyloric stenosis
HP:0002023	Anal atresia
HP:0002024	Malabsorption
HP:0002025	Anal stenosis
HP:0002027	Abdominal pain
HP:0002028	Chronic diarrhea
HP:0002031	Abnormal esophagus morphology
HP:0002032	Esophageal atresia
HP:0002033	Poor suck
HP:0002034	Abnormality of the rectum
HP:0002035	Rectal prolapse
HP:0002036	Hiatus hernia
HP:0002037	Inflammation of the large intestine
HP:0002038	Protein avoidance
HP:0002039	Anorexia
HP:0002040	Esophageal varix
HP:0002041	Intractable diarrhea
HP:0002043	Esophageal stricture
HP:0002044	Zollinger-Ellison syndrome
HP:0002045	Hypothermia
HP:0002046	Heat intolerance
HP:0002047	Malignant hyperthermia
HP:0002048	Renal cortical atrophy
HP:0002049	Proximal renal tubular acidosis
HP:0002050	Macroorchidism, postpubertal
HP:0002054	Heavy supraorbital ridges
HP:0002055	Curved linear dimple below the lower lip
HP:0002056	Abnormality of the glabella
HP:0002057	Prominent glabella
HP:0002058	Myopathic facies
HP:0002059	Cerebral atrophy
HP:0002060	Abnormality of the cerebrum
HP:0002061	Lower limb spasticity
HP:0002062	Morphological abnormality of the pyramidal tract
HP:0002063	Rigidity
HP:0002064	Spastic gait
HP:0002066	Gait ataxia
HP:0002067	Bradykinesia
HP:0002068	Neuromuscular dysphagia
HP:0002069	Generalized tonic-clonic seizures
HP:0002070	Limb ataxia
HP:0002071	Abnormality of extrapyramidal motor function
HP:0002072	Chorea
HP:0002073	Progressive cerebellar ataxia
HP:0002074	Increased neuronal autofluorescent lipopigment
HP:0002075	Dysdiadochokinesis
HP:0002076	Migraine
HP:0002077	Migraine with aura
HP:0002078	Truncal ataxia
HP:0002079	Hypoplasia of the corpus callosum
HP:0002080	Intention tremor
HP:0002083	Migraine without aura
HP:0002084	Encephalocele
HP:0002085	Occipital encephalocele
HP:0002086	Abnormality of the respiratory system
HP:0002087	Abnormality of the upper respiratory tract
HP:0002088	Abnormal lung morphology
HP:0002089	Pulmonary hypoplasia
HP:0002090	Pneumonia
HP:0002091	Restrictive ventilatory defect
HP:0002092	Pulmonary arterial hypertension
HP:0002093	Respiratory insufficiency
HP:0002094	Dyspnea
HP:0002097	Emphysema
HP:0002098	Respiratory distress
HP:0002099	Asthma
HP:0002100	Recurrent aspiration pneumonia
HP:0002101	Abnormal lung lobation
HP:0002102	Pleuritis
HP:0002103	Abnormality of the pleura
HP:0002104	Apnea
HP:0002105	Hemoptysis
HP:0002107	Pneumothorax
HP:0002108	Spontaneous pneumothorax
HP:0002109	obsolete Abnormality of the bronchi
HP:0002110	Bronchiectasis
HP:0002111	Restrictive deficit on pulmonary function testing
HP:0002113	Pulmonary infiltrates
HP:0002118	Abnormality of the cerebral ventricles
HP:0002119	Ventriculomegaly
HP:0002120	Cerebral cortical atrophy
HP:0002121	Absence seizure
HP:0002123	Generalized myoclonic seizures
HP:0002126	Polymicrogyria
HP:0002127	Abnormal upper motor neuron morphology
HP:0002131	Episodic ataxia
HP:0002132	Porencephalic cyst
HP:0002133	Status epilepticus
HP:0002134	Abnormality of the basal ganglia
HP:0002135	Basal ganglia calcification
HP:0002136	Broad-based gait
HP:0002138	Subarachnoid hemorrhage
HP:0002139	Arrhinencephaly
HP:0002140	Ischemic stroke
HP:0002141	Gait imbalance
HP:0002143	Abnormality of the spinal cord
HP:0002144	Tethered cord
HP:0002145	Frontotemporal dementia
HP:0002148	Hypophosphatemia
HP:0002149	Hyperuricemia
HP:0002150	Hypercalciuria
HP:0002151	Increased serum lactate
HP:0002152	Hyperproteinemia
HP:0002153	Hyperkalemia
HP:0002154	Hyperglycinemia
HP:0002155	Hypertriglyceridemia
HP:0002156	Homocystinuria
HP:0002157	Azotemia
HP:0002159	Heparan sulfate excretion in urine
HP:0002160	Hyperhomocystinemia
HP:0002161	Hyperlysinemia
HP:0002162	Low posterior hairline
HP:0002164	Nail dysplasia
HP:0002165	Pterygium of nails
HP:0002166	Impaired vibration sensation in the lower limbs
HP:0002167	Neurological speech impairment
HP:0002168	Scanning speech
HP:0002169	Clonus
HP:0002170	Intracranial hemorrhage
HP:0002171	Gliosis
HP:0002172	Postural instability
HP:0002173	Hypoglycemic seizures
HP:0002174	Postural tremor
HP:0002176	Spinal cord compression
HP:0002179	Opisthotonus
HP:0002180	Neurodegeneration
HP:0002181	Cerebral edema
HP:0002183	Phonophobia
HP:0002185	Neurofibrillary tangles
HP:0002186	Apraxia
HP:0002187	Intellectual disability, profound
HP:0002188	Delayed CNS myelination
HP:0002189	Excessive daytime sleepiness
HP:0002190	Choroid plexus cyst
HP:0002191	Progressive spasticity
HP:0002193	Pseudobulbar behavioral symptoms
HP:0002194	Delayed gross motor development
HP:0002195	Dysgenesis of the cerebellar vermis
HP:0002196	Myelopathy
HP:0002197	Generalized-onset seizure
HP:0002198	Dilated fourth ventricle
HP:0002199	Hypocalcemic seizures
HP:0002200	Pseudobulbar signs
HP:0002202	Pleural effusion
HP:0002203	Respiratory paralysis
HP:0002204	Pulmonary embolism
HP:0002205	Recurrent respiratory infections
HP:0002206	Pulmonary fibrosis
HP:0002207	Diffuse reticular or finely nodular infiltrations
HP:0002208	Coarse hair
HP:0002209	Sparse scalp hair
HP:0002211	White forelock
HP:0002212	Curly hair
HP:0002213	Fine hair
HP:0002215	Sparse axillary hair
HP:0002216	Premature graying of hair
HP:0002217	Slow-growing hair
HP:0002218	Silver-gray hair
HP:0002219	Facial hypertrichosis
HP:0002220	Melanin pigment aggregation in hair shafts
HP:0002221	Absent axillary hair
HP:0002223	Absent eyebrow
HP:0002224	Woolly hair
HP:0002225	Sparse pubic hair
HP:0002226	White eyebrow
HP:0002227	White eyelashes
HP:0002229	Alopecia areata
HP:0002230	Generalized hirsutism
HP:0002231	Sparse body hair
HP:0002232	Patchy alopecia
HP:0002234	Early balding
HP:0002235	Pili canaliculi
HP:0002236	Frontal upsweep of hair
HP:0002239	Gastrointestinal hemorrhage
HP:0002240	Hepatomegaly
HP:0002242	Abnormal intestine morphology
HP:0002243	Protein-losing enteropathy
HP:0002244	Abnormality of the small intestine
HP:0002245	Meckel diverticulum
HP:0002246	Abnormality of the duodenum
HP:0002247	Duodenal atresia
HP:0002248	Hematemesis
HP:0002249	Melena
HP:0002250	Abnormal large intestine morphology
HP:0002251	Aganglionic megacolon
HP:0002253	Colonic diverticula
HP:0002254	Intermittent diarrhea
HP:0002256	Small bowel diverticula
HP:0002257	Chronic rhinitis
HP:0002263	Exaggerated cupid's bow
HP:0002265	Large fleshy ears
HP:0002266	Focal clonic seizures
HP:0002267	Exaggerated startle response
HP:0002268	Paroxysmal dystonia
HP:0002269	Abnormality of neuronal migration
HP:0002270	Abnormality of the autonomic nervous system
HP:0002271	obsolete Autonomic dysregulation
HP:0002273	Tetraparesis
HP:0002275	Poor motor coordination
HP:0002277	Horner syndrome
HP:0002280	Enlarged cisterna magna
HP:0002281	Gray matter heterotopias
HP:0002282	Heterotopia
HP:0002283	Global brain atrophy
HP:0002286	Fair hair
HP:0002287	Progressive alopecia
HP:0002289	Alopecia universalis
HP:0002290	Poliosis
HP:0002292	Frontal balding
HP:0002293	Alopecia of scalp
HP:0002296	Progressive hypotrichosis
HP:0002297	Red hair
HP:0002298	Absent hair
HP:0002299	Brittle hair
HP:0002300	Mutism
HP:0002301	Hemiplegia
HP:0002304	Akinesia
HP:0002305	Athetosis
HP:0002307	Drooling
HP:0002308	Arnold-Chiari malformation
HP:0002310	Orofacial dyskinesia
HP:0002311	Incoordination
HP:0002312	Clumsiness
HP:0002313	Spastic paraparesis
HP:0002314	Degeneration of the lateral corticospinal tracts
HP:0002315	Headache
HP:0002317	Unsteady gait
HP:0002318	Cervical myelopathy
HP:0002321	Vertigo
HP:0002322	Resting tremor
HP:0002323	Anencephaly
HP:0002324	Hydranencephaly
HP:0002326	Transient ischemic attack
HP:0002329	Drowsiness
HP:0002330	Paroxysmal drowsiness
HP:0002331	Recurrent paroxysmal headache
HP:0002332	Lack of peer relationships
HP:0002333	Motor deterioration
HP:0002334	Abnormality of the cerebellar vermis
HP:0002335	Agenesis of cerebellar vermis
HP:0002339	Abnormal caudate nucleus morphology
HP:0002340	Caudate atrophy
HP:0002341	Cervical cord compression
HP:0002342	Intellectual disability, moderate
HP:0002343	Normal pressure hydrocephalus
HP:0002344	Progressive neurologic deterioration
HP:0002345	Action tremor
HP:0002346	Head tremor
HP:0002349	Focal aware seizure
HP:0002350	Cerebellar cyst
HP:0002352	Leukoencephalopathy
HP:0002353	EEG abnormality
HP:0002354	Memory impairment
HP:0002355	Difficulty walking
HP:0002356	Writer's cramp
HP:0002357	Dysphasia
HP:0002359	Frequent falls
HP:0002360	Sleep disturbance
HP:0002361	Psychomotor deterioration
HP:0002362	Shuffling gait
HP:0002363	Abnormality of brainstem morphology
HP:0002365	Hypoplasia of the brainstem
HP:0002366	Abnormal lower motor neuron morphology
HP:0002367	Visual hallucinations
HP:0002370	Poor coordination
HP:0002371	Loss of speech
HP:0002372	Normal interictal EEG
HP:0002373	Febrile seizures
HP:0002374	Diminished movement
HP:0002375	Hypokinesia
HP:0002376	Developmental regression
HP:0002377	obsolete Paraganglioma-related cranial nerve palsy
HP:0002378	Hand tremor
HP:0002380	Fasciculations
HP:0002381	Aphasia
HP:0002383	Encephalitis
HP:0002384	Focal impaired awareness seizure
HP:0002385	Paraparesis
HP:0002389	Cavum septum pellucidum
HP:0002390	Spinal arteriovenous malformation
HP:0002392	EEG with polyspike wave complexes
HP:0002395	Lower limb hyperreflexia
HP:0002396	Cogwheel rigidity
HP:0002398	Degeneration of anterior horn cells
HP:0002401	Stroke-like episode
HP:0002403	Positive Romberg sign
HP:0002404	Thickened superior cerebellar peduncle
HP:0002406	Limb dysmetria
HP:0002408	Cerebral arteriovenous malformation
HP:0002410	Aqueductal stenosis
HP:0002411	Myokymia
HP:0002414	Spina bifida
HP:0002415	Leukodystrophy
HP:0002416	Subependymal cysts
HP:0002418	Abnormality of midbrain morphology
HP:0002419	Molar tooth sign on MRI
HP:0002421	Poor head control
HP:0002423	Long-tract signs
HP:0002425	Anarthria
HP:0002427	Motor aphasia
HP:0002435	Meningocele
HP:0002436	Occipital meningocele
HP:0002438	Cerebellar malformation
HP:0002439	Frontolimbic dementia
HP:0002442	Dyscalculia
HP:0002444	Hypothalamic hamartoma
HP:0002445	Tetraplegia
HP:0002446	Astrocytosis
HP:0002448	Progressive encephalopathy
HP:0002450	Abnormal motor neuron morphology
HP:0002451	Limb dystonia
HP:0002453	Abnormal globus pallidus morphology
HP:0002454	Eye of the tiger anomaly of globus pallidus
HP:0002457	Abnormal head movements
HP:0002459	obsolete Dysautonomia
HP:0002460	Distal muscle weakness
HP:0002461	Dense calcifications in the cerebellar dentate nucleus
HP:0002463	Language impairment
HP:0002464	Spastic dysarthria
HP:0002465	Poor speech
HP:0002470	Nonprogressive cerebellar ataxia
HP:0002472	Small cerebral cortex
HP:0002474	Expressive language delay
HP:0002475	Myelomeningocele
HP:0002476	Primitive reflex
HP:0002478	Progressive spastic quadriplegia
HP:0002480	Hepatic encephalopathy
HP:0002483	Bulbar signs
HP:0002486	Myotonia
HP:0002487	Hyperkinesis
HP:0002488	Acute leukemia
HP:0002490	Increased CSF lactate
HP:0002491	Spasticity of facial muscles
HP:0002492	Abnormality of the corticospinal tract
HP:0002493	Upper motor neuron dysfunction
HP:0002494	Abnormal rapid eye movement sleep
HP:0002495	Impaired vibratory sensation
HP:0002497	Spastic ataxia
HP:0002500	Abnormality of the cerebral white matter
HP:0002501	Spasticity of pharyngeal muscles
HP:0002503	Spinocerebellar tract degeneration
HP:0002504	Calcification of the small brain vessels
HP:0002505	Progressive inability to walk
HP:0002506	Diffuse cerebral atrophy
HP:0002507	Semilobar holoprosencephaly
HP:0002508	Brainstem dysplasia
HP:0002509	Limb hypertonia
HP:0002510	Spastic tetraplegia
HP:0002511	Alzheimer disease
HP:0002512	Brain stem compression
HP:0002514	Cerebral calcification
HP:0002515	Waddling gait
HP:0002516	Increased intracranial pressure
HP:0002518	Abnormality of the periventricular white matter
HP:0002519	Hypnagogic hallucinations
HP:0002521	Hypsarrhythmia
HP:0002522	Areflexia of lower limbs
HP:0002524	Cataplexy
HP:0002526	Deficit in nonword repetition
HP:0002527	Falls
HP:0002528	Granulovacuolar degeneration
HP:0002529	Neuronal loss in central nervous system
HP:0002530	Axial dystonia
HP:0002533	Abnormal posturing
HP:0002536	Abnormal cortical gyration
HP:0002538	Abnormality of the cerebral cortex
HP:0002539	Cortical dysplasia
HP:0002540	Inability to walk
HP:0002542	Olivopontocerebellar atrophy
HP:0002544	Retrocollis
HP:0002545	Patchy demyelination of subcortical white matter
HP:0002546	Incomprehensible speech
HP:0002548	Parkinsonism with favorable response to dopaminergic medication
HP:0002549	Deficit in phonologic short-term memory
HP:0002550	Absent facial hair
HP:0002552	Trichodysplasia
HP:0002553	Highly arched eyebrow
HP:0002555	Absent pubic hair
HP:0002557	Hypoplastic nipples
HP:0002558	Supernumerary nipple
HP:0002561	Absent nipple
HP:0002562	Low-set nipples
HP:0002563	Constrictive pericarditis
HP:0002564	obsolete Malformation of the heart and great vessels
HP:0002566	Intestinal malrotation
HP:0002570	Steatorrhea
HP:0002571	Achalasia
HP:0002572	Episodic vomiting
HP:0002573	Hematochezia
HP:0002574	Episodic abdominal pain
HP:0002575	Tracheoesophageal fistula
HP:0002576	Intussusception
HP:0002577	Abnormality of the stomach
HP:0002578	Gastroparesis
HP:0002579	Gastrointestinal dysmotility
HP:0002580	Volvulus
HP:0002582	Chronic atrophic gastritis
HP:0002583	Colitis
HP:0002584	Intestinal bleeding
HP:0002585	Abnormality of the peritoneum
HP:0002586	Peritonitis
HP:0002587	Projectile vomiting
HP:0002588	Duodenal ulcer
HP:0002589	Gastrointestinal atresia
HP:0002590	Paralytic ileus
HP:0002591	Polyphagia
HP:0002592	Gastric ulcer
HP:0002593	Intestinal lymphangiectasia
HP:0002594	Pancreatic hypoplasia
HP:0002595	Ileus
HP:0002597	Abnormality of the vasculature
HP:0002599	Head titubation
HP:0002600	Hyporeflexia of lower limbs
HP:0002601	Paresis of extensor muscles of the big toe
HP:0002604	Gastrointestinal telangiectasia
HP:0002605	Hepatic necrosis
HP:0002607	Bowel incontinence
HP:0002608	Celiac disease
HP:0002611	Cholestatic liver disease
HP:0002612	Congenital hepatic fibrosis
HP:0002613	Biliary cirrhosis
HP:0002614	Hepatic periportal necrosis
HP:0002615	Hypotension
HP:0002616	Aortic root aneurysm
HP:0002617	Dilatation
HP:0002619	Varicose veins
HP:0002621	Atherosclerosis
HP:0002622	obsolete Dissecting aortic dilatation
HP:0002623	Overriding aorta
HP:0002624	Abnormal venous morphology
HP:0002625	Deep venous thrombosis
HP:0002626	Venous varicosities of celiac and mesenteric vessels
HP:0002627	Right aortic arch with mirror image branching
HP:0002629	Gastrointestinal arteriovenous malformation
HP:0002630	Fat malabsorption
HP:0002631	obsolete Dilatation of ascending aorta
HP:0002632	Low-to-normal blood pressure
HP:0002633	Vasculitis
HP:0002634	Arteriosclerosis
HP:0002635	Type IV atherosclerotic lesion
HP:0002636	Dilatation of an abdominal artery
HP:0002637	Cerebral ischemia
HP:0002638	Superficial thrombophlebitis
HP:0002639	Budd-Chiari syndrome
HP:0002640	Hypertension associated with pheochromocytoma
HP:0002641	Peripheral thrombosis
HP:0002642	Arteriovenous fistulas of celiac and mesenteric vessels
HP:0002643	Neonatal respiratory distress
HP:0002644	Abnormality of pelvic girdle bone morphology
HP:0002645	Wormian bones
HP:0002647	Aortic dissection
HP:0002648	Abnormality of calvarial morphology
HP:0002650	Scoliosis
HP:0002651	Spondyloepimetaphyseal dysplasia
HP:0002652	Skeletal dysplasia
HP:0002653	Bone pain
HP:0002654	Multiple epiphyseal dysplasia
HP:0002655	Spondyloepiphyseal dysplasia
HP:0002656	Epiphyseal dysplasia
HP:0002657	Spondylometaphyseal dysplasia
HP:0002659	Increased susceptibility to fractures
HP:0002661	Painless fractures due to injury
HP:0002663	Delayed epiphyseal ossification
HP:0002664	Neoplasm
HP:0002665	Lymphoma
HP:0002666	Pheochromocytoma
HP:0002667	Nephroblastoma
HP:0002668	Paraganglioma
HP:0002669	Osteosarcoma
HP:0002671	Basal cell carcinoma
HP:0002672	Gastrointestinal carcinoma
HP:0002673	Coxa valga
HP:0002676	Cloverleaf skull
HP:0002677	Small foramen magnum
HP:0002678	Skull asymmetry
HP:0002679	Abnormality of the sella turcica
HP:0002680	J-shaped sella turcica
HP:0002681	Deformed sella turcica
HP:0002682	Broad skull
HP:0002683	Abnormality of the calvaria
HP:0002684	Thickened calvaria
HP:0002686	Prenatal maternal abnormality
HP:0002687	Abnormality of frontal sinus
HP:0002688	Absent frontal sinuses
HP:0002689	Absent paranasal sinuses
HP:0002690	Large sella turcica
HP:0002691	Platybasia
HP:0002692	Hypoplastic facial bones
HP:0002693	Abnormality of the skull base
HP:0002694	Sclerosis of skull base
HP:0002695	Symmetrical, oval parietal bone defects
HP:0002696	Abnormal parietal bone morphology
HP:0002697	Parietal foramina
HP:0002699	Abnormality of the foramen magnum
HP:0002700	Large foramen magnum
HP:0002703	Abnormality of skull ossification
HP:0002705	High, narrow palate
HP:0002707	Palate telangiectasia
HP:0002708	Prominent median palatal raphe
HP:0002710	Commissural lip pit
HP:0002711	Exaggerated median tongue furrow
HP:0002714	Downturned corners of mouth
HP:0002715	Abnormality of the immune system
HP:0002716	Lymphadenopathy
HP:0002717	Adrenal overactivity
HP:0002718	Recurrent bacterial infections
HP:0002719	Recurrent infections
HP:0002720	Decreased circulating IgA level
HP:0002721	Immunodeficiency
HP:0002722	Recurrent abscess formation
HP:0002723	Absence of bactericidal oxidative respiratory burst in phagocytes
HP:0002724	Recurrent Aspergillus infections
HP:0002725	Systemic lupus erythematosus
HP:0002726	Recurrent Staphylococcus aureus infections
HP:0002728	Chronic mucocutaneous candidiasis
HP:0002729	Follicular hyperplasia
HP:0002730	Chronic noninfectious lymphadenopathy
HP:0002731	Decreased lymphocyte apoptosis
HP:0002732	Lymph node hypoplasia
HP:0002733	Abnormality of the lymph nodes
HP:0002737	Thick skull base
HP:0002738	Hypoplastic frontal sinuses
HP:0002740	Recurrent E. coli infections
HP:0002741	Recurrent Serratia marcescens infections
HP:0002742	Recurrent Klebsiella infections
HP:0002743	Recurrent enteroviral infections
HP:0002744	Bilateral cleft lip and palate
HP:0002745	Oral leukoplakia
HP:0002747	Respiratory insufficiency due to muscle weakness
HP:0002748	Rickets
HP:0002749	Osteomalacia
HP:0002750	Delayed skeletal maturation
HP:0002751	Kyphoscoliosis
HP:0002752	Sparse bone trabeculae
HP:0002753	Thin bony cortex
HP:0002754	Osteomyelitis
HP:0002755	obsolete Osteomyelitis due to immunodeficiency
HP:0002756	Pathologic fracture
HP:0002757	Recurrent fractures
HP:0002758	Osteoarthritis
HP:0002761	Generalized joint laxity
HP:0002762	Multiple exostoses
HP:0002763	Abnormal cartilage morphology
HP:0002764	Stippled chondral calcification
HP:0002766	Relatively short spine
HP:0002773	obsolete Small vertebral bodies
HP:0002777	Tracheal stenosis
HP:0002778	Abnormal trachea morphology
HP:0002779	Tracheomalacia
HP:0002780	Bronchomalacia
HP:0002781	Upper airway obstruction
HP:0002783	Recurrent lower respiratory tract infections
HP:0002786	Tracheobronchomalacia
HP:0002787	Tracheal calcification
HP:0002788	Recurrent upper respiratory tract infections
HP:0002789	Tachypnea
HP:0002790	Neonatal breathing dysregulation
HP:0002791	Hypoventilation
HP:0002792	Reduced vital capacity
HP:0002793	Abnormal pattern of respiration
HP:0002795	Functional respiratory abnormality
HP:0002797	Osteolysis
HP:0002803	Congenital contracture
HP:0002804	Arthrogryposis multiplex congenita
HP:0002805	Accelerated bone age after puberty
HP:0002808	Kyphosis
HP:0002810	Dumbbell-shaped metaphyses
HP:0002812	Coxa vara
HP:0002813	Abnormality of limb bone morphology
HP:0002814	Abnormality of the lower limb
HP:0002815	Abnormality of the knee
HP:0002816	Genu recurvatum
HP:0002817	Abnormality of the upper limb
HP:0002818	Abnormality of the radius
HP:0002821	Neuropathic arthropathy
HP:0002822	Hyperplasia of the femoral trochanters
HP:0002823	Abnormality of femur morphology
HP:0002825	Caudal appendage
HP:0002826	Halberd-shaped pelvis
HP:0002827	Hip dislocation
HP:0002828	Multiple joint contractures
HP:0002829	Arthralgia
HP:0002831	Long coccyx
HP:0002832	Calcific stippling
HP:0002833	Cystic angiomatosis of bone
HP:0002834	Flared femoral metaphysis
HP:0002835	Aspiration
HP:0002836	Bladder exstrophy
HP:0002837	Recurrent bronchitis
HP:0002839	Urinary bladder sphincter dysfunction
HP:0002840	Lymphadenitis
HP:0002841	Recurrent fungal infections
HP:0002842	Recurrent Burkholderia cepacia infections
HP:0002843	Abnormal T cell morphology
HP:0002845	obsolete Increased proportion of peripheral CD3+ T cells
HP:0002846	Abnormal B cell morphology
HP:0002847	Impaired memory B cell generation
HP:0002848	Specific anti-polysaccharide antibody deficiency
HP:0002849	Absence of lymph node germinal center
HP:0002850	Decreased circulating total IgM
HP:0002851	Elevated proportion of CD4-negative, CD8-negative, alpha-beta regulatory T cells
HP:0002853	Increased proportion of HLA DR+ T cells
HP:0002857	Genu valgum
HP:0002858	Meningioma
HP:0002859	Rhabdomyosarcoma
HP:0002860	Squamous cell carcinoma
HP:0002861	Melanoma
HP:0002862	Bladder carcinoma
HP:0002863	Myelodysplasia
HP:0002864	Paraganglioma of head and neck
HP:0002865	Medullary thyroid carcinoma
HP:0002866	Hypoplastic iliac wing
HP:0002867	Abnormality of the ilium
HP:0002868	Narrow iliac wings
HP:0002869	Flared iliac wings
HP:0002870	Obstructive sleep apnea
HP:0002871	Central apnea
HP:0002872	Apneic episodes precipitated by illness, fatigue, stress
HP:0002875	Exertional dyspnea
HP:0002876	Episodic tachypnea
HP:0002877	Nocturnal hypoventilation
HP:0002878	Respiratory failure
HP:0002879	Anisospondyly
HP:0002880	obsolete Respiratory difficulties
HP:0002882	Sudden episodic apnea
HP:0002883	Hyperventilation
HP:0002884	Hepatoblastoma
HP:0002885	Medulloblastoma
HP:0002886	Vagal paraganglioma
HP:0002888	Ependymoma
HP:0002890	Thyroid carcinoma
HP:0002891	Uterine leiomyosarcoma
HP:0002893	Pituitary adenoma
HP:0002894	Neoplasm of the pancreas
HP:0002895	Papillary thyroid carcinoma
HP:0002896	Neoplasm of the liver
HP:0002897	Parathyroid adenoma
HP:0002898	Embryonal neoplasm
HP:0002900	Hypokalemia
HP:0002901	Hypocalcemia
HP:0002902	Hyponatremia
HP:0002904	Hyperbilirubinemia
HP:0002905	Hyperphosphatemia
HP:0002907	Microscopic hematuria
HP:0002908	Conjugated hyperbilirubinemia
HP:0002909	Generalized aminoaciduria
HP:0002910	Elevated hepatic transaminase
HP:0002912	Methylmalonic acidemia
HP:0002913	Myoglobinuria
HP:0002914	Hyperchloriduria
HP:0002916	Abnormality of chromosome segregation
HP:0002917	Hypomagnesemia
HP:0002918	Hypermagnesemia
HP:0002919	Ketonuria
HP:0002920	Decreased circulating ACTH level
HP:0002921	Abnormality of the cerebrospinal fluid
HP:0002922	Increased CSF protein
HP:0002923	Rheumatoid factor positive
HP:0002924	obsolete Decreased circulating aldosterone level
HP:0002925	Increased thyroid-stimulating hormone level
HP:0002926	Abnormality of thyroid physiology
HP:0002927	Histidinuria
HP:0002928	Decreased activity of the pyruvate dehydrogenase complex
HP:0002929	Leydig cell insensitivity to gonadotropin
HP:0002930	Thyroid hormone receptor defect
HP:0002932	Aldehyde oxidase deficiency
HP:0002933	Ventral hernia
HP:0002936	Distal sensory impairment
HP:0002937	Hemivertebrae
HP:0002938	Lumbar hyperlordosis
HP:0002942	Thoracic kyphosis
HP:0002943	Thoracic scoliosis
HP:0002944	Thoracolumbar scoliosis
HP:0002945	Intervertebral space narrowing
HP:0002946	Supernumerary vertebrae
HP:0002947	Cervical kyphosis
HP:0002948	Vertebral fusion
HP:0002949	Fused cervical vertebrae
HP:0002951	Partial absence of cerebellar vermis
HP:0002953	Vertebral compression fractures
HP:0002955	Granulomatosis
HP:0002958	Immune dysregulation
HP:0002959	Impaired Ig class switch recombination
HP:0002960	Autoimmunity
HP:0002961	Dysgammaglobulinemia
HP:0002963	Abnormal delayed hypersensitivity skin test
HP:0002965	Cutaneous anergy
HP:0002967	Cubitus valgus
HP:0002970	Genu varum
HP:0002971	Absent microvilli on the surface of peripheral blood lymphocytes
HP:0002972	Reduced delayed hypersensitivity
HP:0002973	Abnormality of the forearm
HP:0002974	Radioulnar synostosis
HP:0002977	Aplasia/Hypoplasia involving the central nervous system
HP:0002979	Bowing of the legs
HP:0002980	Femoral bowing
HP:0002981	Abnormality of the calf
HP:0002982	Tibial bowing
HP:0002983	Micromelia
HP:0002984	Hypoplasia of the radius
HP:0002986	Radial bowing
HP:0002987	Elbow flexion contracture
HP:0002990	Fibular aplasia
HP:0002991	Abnormality of fibula morphology
HP:0002992	Abnormality of tibia morphology
HP:0002996	Limited elbow movement
HP:0002997	Abnormality of the ulna
HP:0002999	Patellar dislocation
HP:0003001	Glomus jugular tumor
HP:0003002	Breast carcinoma
HP:0003003	Colon cancer
HP:0003005	Ganglioneuroma
HP:0003006	Neuroblastoma
HP:0003009	Enhanced neurotoxicity of vincristine
HP:0003010	Prolonged bleeding time
HP:0003011	Abnormality of the musculature
HP:0003013	Bulging epiphyses
HP:0003015	Flared metaphysis
HP:0003016	Metaphyseal widening
HP:0003019	Abnormality of the wrist
HP:0003020	Enlargement of the wrists
HP:0003021	Metaphyseal cupping
HP:0003022	Hypoplasia of the ulna
HP:0003023	Bowing of limbs due to multiple fractures
HP:0003025	Metaphyseal irregularity
HP:0003026	Short long bone
HP:0003027	Mesomelia
HP:0003028	Abnormality of the ankles
HP:0003029	Enlargement of the ankles
HP:0003031	Ulnar bowing
HP:0003034	Diaphyseal sclerosis
HP:0003037	Enlarged joints
HP:0003038	Fibular hypoplasia
HP:0003040	Arthropathy
HP:0003041	Humeroradial synostosis
HP:0003042	Elbow dislocation
HP:0003043	Abnormality of the shoulder
HP:0003044	Shoulder flexion contracture
HP:0003045	Abnormality of the patella
HP:0003048	Radial head subluxation
HP:0003049	Ulnar deviation of the wrist
HP:0003051	Enlarged metaphyses
HP:0003053	Epiphyseal deformities of tubular bones
HP:0003057	Tetraamelia
HP:0003059	Abnormality of the radioulnar joints
HP:0003063	Abnormality of the humerus
HP:0003065	Patellar hypoplasia
HP:0003066	Limited knee extension
HP:0003067	Madelung deformity
HP:0003068	Madelung-like forearm deformities
HP:0003070	Elbow ankylosis
HP:0003071	Flattened epiphysis
HP:0003072	Hypercalcemia
HP:0003073	Hypoalbuminemia
HP:0003074	Hyperglycemia
HP:0003075	Hypoproteinemia
HP:0003076	Glycosuria
HP:0003077	Hyperlipidemia
HP:0003079	Defective DNA repair after ultraviolet radiation damage
HP:0003080	Hydroxyprolinuria
HP:0003081	Increased urinary potassium
HP:0003083	Dislocated radial head
HP:0003084	Fractures of the long bones
HP:0003085	Long fibula
HP:0003086	Acromesomelia
HP:0003088	Premature osteoarthritis
HP:0003089	Hamstring contractures
HP:0003090	Hypoplasia of the capital femoral epiphysis
HP:0003091	Trophic limb changes
HP:0003093	Limited hip extension
HP:0003095	Septic arthritis
HP:0003097	Short femur
HP:0003099	Fibular overgrowth
HP:0003100	Slender long bone
HP:0003102	Increased carrying angle
HP:0003103	Abnormal cortical bone morphology
HP:0003105	Protuberances at ends of long bones
HP:0003106	Subperiosteal bone resorption
HP:0003107	Abnormality of cholesterol metabolism
HP:0003108	Hyperglycinuria
HP:0003109	Hyperphosphaturia
HP:0003110	Abnormality of urine homeostasis
HP:0003111	Abnormality of ion homeostasis
HP:0003112	Abnormality of serum amino acid level
HP:0003113	Hypochloremia
HP:0003114	obsolete Abnormal cardiological findings
HP:0003115	Abnormal EKG
HP:0003116	Abnormal echocardiogram
HP:0003117	Abnormality of circulating hormone level
HP:0003118	Increased circulating cortisol level
HP:0003119	Abnormality of lipid metabolism
HP:0003121	Limb joint contracture
HP:0003124	Hypercholesterolemia
HP:0003125	Reduced factor VIII activity
HP:0003126	Low-molecular-weight proteinuria
HP:0003127	Hypocalciuria
HP:0003128	Lactic acidosis
HP:0003130	Abnormal peripheral myelination
HP:0003131	Cystinuria
HP:0003133	Abnormality of the spinocerebellar tracts
HP:0003134	Abnormality of peripheral nerve conduction
HP:0003137	Prolinuria
HP:0003138	Increased blood urea nitrogen
HP:0003139	Panhypogammaglobulinemia
HP:0003140	T-wave inversion in the right precordial leads
HP:0003141	Increased LDL cholesterol concentration
HP:0003142	Excessive purine production
HP:0003144	Increased serum serotonin
HP:0003145	Decreased adenosylcobalamin
HP:0003146	Hypocholesterolemia
HP:0003148	Elevated serum acid phosphatase
HP:0003149	Hyperuricosuria
HP:0003150	Glutaric aciduria
HP:0003152	Increased serum 1,25-dihydroxyvitamin D3
HP:0003153	Cystathioninuria
HP:0003154	Increased circulating ACTH level
HP:0003155	Elevated alkaline phosphatase
HP:0003158	Hyposthenuria
HP:0003159	Hyperoxaluria
HP:0003160	Abnormal isoelectric focusing of serum transferrin
HP:0003161	4-Hydroxyphenylpyruvic aciduria
HP:0003162	Fasting hypoglycemia
HP:0003163	Elevated urinary delta-aminolevulinic acid
HP:0003164	Hypothalamic gonadotropin-releasing hormone deficiency
HP:0003165	Elevated circulating parathyroid hormone level
HP:0003166	Increased urinary taurine
HP:0003167	Carnosinuria
HP:0003168	Dibasicaminoaciduria
HP:0003170	Abnormality of the acetabulum
HP:0003172	Abnormality of the pubic bone
HP:0003173	Hypoplastic pubic bone
HP:0003174	Abnormality of the ischium
HP:0003175	Hypoplastic ischia
HP:0003177	Squared iliac bones
HP:0003179	Protrusio acetabuli
HP:0003180	Flat acetabular roof
HP:0003182	Shallow acetabular fossae
HP:0003183	Wide pubic symphysis
HP:0003184	Decreased hip abduction
HP:0003185	Short sacroiliac notch
HP:0003186	Inverted nipples
HP:0003187	Breast hypoplasia
HP:0003189	Long nose
HP:0003191	Cleft ala nasi
HP:0003193	Allergic rhinitis
HP:0003194	Short nasal bridge
HP:0003196	Short nose
HP:0003198	Myopathy
HP:0003199	Decreased muscle mass
HP:0003200	Ragged-red muscle fibers
HP:0003201	Rhabdomyolysis
HP:0003202	Skeletal muscle atrophy
HP:0003203	Impaired oxidative burst
HP:0003204	Intracellular accumulation of autofluorescent lipopigment storage material
HP:0003205	Curvilinear intracellular accumulation of autofluorescent lipopigment storage material
HP:0003206	Decreased activity of NADPH oxidase
HP:0003207	Arterial calcification
HP:0003208	Fingerprint intracellular accumulation of autofluorescent lipopigment storage material
HP:0003209	Decreased pyruvate carboxylase activity
HP:0003210	Decreased methylmalonyl-CoA mutase activity
HP:0003212	Increased IgE level
HP:0003213	Deficient excision of UV-induced pyrimidine dimers in DNA
HP:0003214	Prolonged G2 phase of cell cycle
HP:0003215	Dicarboxylic aciduria
HP:0003216	Generalized amyloid deposition
HP:0003217	Hyperglutaminemia
HP:0003218	Oroticaciduria
HP:0003219	Ethylmalonic aciduria
HP:0003220	Abnormality of chromosome stability
HP:0003221	Chromosomal breakage induced by crosslinking agents
HP:0003223	Decreased methylcobalamin
HP:0003224	Increased cellular sensitivity to UV light
HP:0003225	Reduced coagulation factor V activity
HP:0003226	Rectilinear intracellular accumulation of autofluorescent lipopigment storage material
HP:0003228	Hypernatremia
HP:0003231	Hypertyrosinemia
HP:0003232	Mitochondrial malic enzyme reduced
HP:0003233	Decreased HDL cholesterol concentration
HP:0003234	Decreased plasma carnitine
HP:0003235	Hypermethioninemia
HP:0003236	Elevated serum creatine phosphokinase
HP:0003237	Increased IgG level
HP:0003238	Hyperpepsinogenemia I
HP:0003239	Phosphoethanolaminuria
HP:0003240	Increased phosphoribosylpyrophosphate synthetase
HP:0003241	External genital hypoplasia
HP:0003244	Penile hypospadias
HP:0003246	Prominent scrotal raphe
HP:0003247	Overgrowth of external genitalia
HP:0003248	Gonadal tissue inappropriate for external genitalia or chromosomal sex
HP:0003249	Genital ulcers
HP:0003250	Aplasia of the vagina
HP:0003251	Male infertility
HP:0003252	Anteriorly displaced genitalia
HP:0003254	Abnormality of DNA repair
HP:0003256	Abnormality of the coagulation cascade
HP:0003258	Glyoxalase deficiency
HP:0003259	Elevated serum creatinine
HP:0003260	Hydroxyprolinemia
HP:0003261	Increased IgA level
HP:0003262	Smooth muscle antibody positivity
HP:0003264	Deficiency of N-acetylglucosamine-1-phosphotransferase
HP:0003265	Neonatal hyperbilirubinemia
HP:0003267	Reduced orotidine 5-prime phosphate decarboxylase activity
HP:0003268	Argininuria
HP:0003269	Sudanophilic leukodystrophy
HP:0003270	Abdominal distention
HP:0003271	Visceromegaly
HP:0003272	Abnormality of the hip bone
HP:0003273	Hip contracture
HP:0003274	Hypoplastic acetabulae
HP:0003275	Narrow pelvis bone
HP:0003276	Pelvic bone exostoses
HP:0003277	Constricted iliac wings
HP:0003278	Square pelvis bone
HP:0003279	Coxa magna
HP:0003281	Increased serum ferritin
HP:0003282	Low alkaline phosphatase
HP:0003286	Cystathioninemia
HP:0003287	Abnormality of mitochondrial metabolism
HP:0003288	Mitochondrial propionyl-CoA carboxylase defect
HP:0003292	Decreased serum leptin
HP:0003295	obsolete Impaired FSH and LH secretion
HP:0003296	Hyperthreoninuria
HP:0003297	Hyperlysinuria
HP:0003298	Spina bifida occulta
HP:0003300	Ovoid vertebral bodies
HP:0003301	Irregular vertebral endplates
HP:0003302	Spondylolisthesis
HP:0003304	Spondylolysis
HP:0003305	Block vertebrae
HP:0003306	Spinal rigidity
HP:0003307	Hyperlordosis
HP:0003308	Cervical subluxation
HP:0003309	Ovoid thoracolumbar vertebrae
HP:0003310	Abnormality of the odontoid process
HP:0003311	Hypoplasia of the odontoid process
HP:0003312	Abnormal form of the vertebral bodies
HP:0003316	Butterfly vertebrae
HP:0003318	Cervical spine hypermobility
HP:0003319	Abnormality of the cervical spine
HP:0003320	C1-C2 subluxation
HP:0003321	Biconcave flattened vertebrae
HP:0003323	Progressive muscle weakness
HP:0003324	Generalized muscle weakness
HP:0003325	Limb-girdle muscle weakness
HP:0003326	Myalgia
HP:0003327	Axial muscle weakness
HP:0003328	Abnormal hair laboratory examination
HP:0003329	Hair shafts flattened at irregular intervals and twisted through 180 degrees about their axes
HP:0003330	Abnormal bone structure
HP:0003332	Absent primary metaphyseal spongiosa
HP:0003333	Increased serum beta-hexosaminidase
HP:0003334	Elevated circulating catecholamine level
HP:0003335	obsolete Low gonadotropins (secondary hypogonadism)
HP:0003336	Abnormal enchondral ossification
HP:0003337	Reduced prothrombin consumption
HP:0003338	Focal necrosis of right ventricular muscle cells
HP:0003339	Pyrimidine-responsive megaloblastic anemia
HP:0003340	obsolete Abnormal dermatological laboratory findings
HP:0003341	Junctional split
HP:0003343	Glutathione synthetase deficiency
HP:0003344	3-Methylglutaric aciduria
HP:0003345	Elevated urinary norepinephrine
HP:0003347	Impaired lymphocyte transformation with phytohemagglutinin
HP:0003348	Hyperalaninemia
HP:0003349	Low cholesterol esterification rates
HP:0003351	Decreased circulating renin level
HP:0003352	Endopolyploidy on chromosome studies of bone marrow
HP:0003353	Propionyl-CoA carboxylase deficiency
HP:0003354	Hyperthreoninemia
HP:0003355	Aminoaciduria
HP:0003357	Thymic hormone decreased
HP:0003358	Elevated intracellular cystine
HP:0003359	Decreased urinary sulfate
HP:0003361	Tryptophanuria
HP:0003362	Increased VLDL cholesterol concentration
HP:0003363	Abdominal situs inversus
HP:0003365	Arthralgia of the hip
HP:0003366	Abnormality of the femoral neck or head region
HP:0003367	Abnormality of the femoral neck
HP:0003368	Abnormality of the femoral head
HP:0003370	Flat capital femoral epiphysis
HP:0003371	Enlargement of the proximal femoral epiphysis
HP:0003375	Narrow greater sacrosciatic notches
HP:0003376	Steppage gait
HP:0003378	Axonal degeneration/regeneration
HP:0003380	Decreased number of peripheral myelinated nerve fibers
HP:0003382	Hypertrophic nerve changes
HP:0003383	Onion bulb formation
HP:0003384	Peripheral axonal atrophy
HP:0003387	Decreased number of large peripheral myelinated nerve fibers
HP:0003388	Easy fatigability
HP:0003390	Sensory axonal neuropathy
HP:0003391	Gowers sign
HP:0003392	First dorsal interossei muscle weakness
HP:0003393	Thenar muscle atrophy
HP:0003394	Muscle cramps
HP:0003396	Syringomyelia
HP:0003397	Generalized hypotonia due to defect at the neuromuscular junction
HP:0003398	Abnormal synaptic transmission at the neuromuscular junction
HP:0003400	Basal lamina onion bulb formation
HP:0003401	Paresthesia
HP:0003402	Decreased miniature endplate potentials
HP:0003403	EMG: decremental response of compound muscle action potential to repetitive nerve stimulation
HP:0003405	Diffuse axonal swelling
HP:0003406	Peripheral nerve compression
HP:0003409	Distal sensory impairment of all modalities
HP:0003411	Proximal femoral metaphyseal irregularity
HP:0003413	Atlantoaxial abnormality
HP:0003414	Atlantoaxial dislocation
HP:0003416	Spinal canal stenosis
HP:0003417	Coronal cleft vertebrae
HP:0003418	Back pain
HP:0003419	Low back pain
HP:0003421	obsolete Platyspondyly (childhood)
HP:0003422	Vertebral segmentation defect
HP:0003423	Thoracolumbar kyphoscoliosis
HP:0003426	First dorsal interossei muscle atrophy
HP:0003427	Thenar muscle weakness
HP:0003429	CNS hypomyelination
HP:0003431	Decreased motor nerve conduction velocity
HP:0003434	Sensory ataxic neuropathy
HP:0003435	Cold-induced hand cramps
HP:0003436	Prolonged miniature endplate currents
HP:0003438	Absent Achilles reflex
HP:0003440	Horizontal sacrum
HP:0003443	Decreased size of nerve terminals
HP:0003444	EMG: chronic denervation signs
HP:0003445	EMG: neuropathic changes
HP:0003447	Axonal loss
HP:0003448	Decreased sensory nerve conduction velocity
HP:0003449	Cold-induced muscle cramps
HP:0003450	Axonal regeneration
HP:0003451	Increased rate of premature chromosome condensation
HP:0003452	Increased serum iron
HP:0003453	Antineutrophil antibody positivity
HP:0003454	Platelet antibody positive
HP:0003455	Elevated long chain fatty acids
HP:0003456	Low urinary cyclic AMP response to PTH administration
HP:0003457	EMG abnormality
HP:0003458	EMG: myopathic abnormalities
HP:0003459	Polyclonal elevation of IgM
HP:0003460	Decreased circulating total IgA
HP:0003461	Increased urinary O-linked sialopeptides
HP:0003462	Elevated 8-dehydrocholesterol
HP:0003463	Increased extraneuronal autofluorescent lipopigment
HP:0003464	Abnormal cholesterol homeostasis
HP:0003465	Elevated 8(9)-cholestenol
HP:0003466	Paradoxical increased cortisol secretion on dexamethasone suppression test
HP:0003467	Atlantoaxial instability
HP:0003468	Abnormal vertebral morphology
HP:0003469	Peripheral dysmyelination
HP:0003470	Paralysis
HP:0003472	Hypocalcemic tetany
HP:0003473	Fatigable weakness
HP:0003474	Sensory impairment
HP:0003477	Peripheral axonal neuropathy
HP:0003481	Segmental peripheral demyelination/remyelination
HP:0003482	EMG: axonal abnormality
HP:0003484	Upper limb muscle weakness
HP:0003487	Babinski sign
HP:0003489	Acute episodes of neuropathic symptoms
HP:0003490	Defective dehydrogenation of isovaleryl CoA and butyryl CoA
HP:0003491	Elevated urine pyrophosphate
HP:0003492	High urinary gonadotropin level
HP:0003493	Antinuclear antibody positivity
HP:0003494	obsolete Loss of heterozygosity, multiple chromosomes
HP:0003495	GM2-ganglioside accumulation
HP:0003496	Increased IgM level
HP:0003498	Disproportionate short stature
HP:0003502	Mild short stature
HP:0003508	Proportionate short stature
HP:0003510	Severe short stature
HP:0003513	Reduced ratio of renal calcium clearance to creatinine clearance
HP:0003514	Deficiency or absence of cytochrome b(-245)
HP:0003517	Birth length greater than 97th percentile
HP:0003521	Disproportionate short-trunk short stature
HP:0003524	Decreased methionine synthase activity
HP:0003526	Orotic acid crystalluria
HP:0003527	Hyperprostaglandinuria
HP:0003528	Elevated calcitonin
HP:0003529	Parathormone-independent increased renal tubular calcium reabsorption
HP:0003530	Glutaric acidemia
HP:0003532	Ornithinuria
HP:0003533	Delayed oxidation of acetaldehyde
HP:0003534	Reduced xanthine dehydrogenase activity
HP:0003535	3-Methylglutaconic aciduria
HP:0003536	Decreased fumarate hydratase activity
HP:0003537	Hypouricemia
HP:0003538	Increased serum iduronate sulfatase activity
HP:0003540	Impaired platelet aggregation
HP:0003541	Urinary glycosaminoglycan excretion
HP:0003542	Increased serum pyruvate
HP:0003546	Exercise intolerance
HP:0003547	Shoulder girdle muscle weakness
HP:0003548	Subsarcolemmal accumulations of abnormally shaped mitochondria
HP:0003549	Abnormality of connective tissue
HP:0003550	Predominantly lower limb lymphedema
HP:0003551	Difficulty climbing stairs
HP:0003552	Muscle stiffness
HP:0003553	obsolete Cellulitis due to immunodeficiency
HP:0003554	Type 2 muscle fiber atrophy
HP:0003555	Muscle fiber splitting
HP:0003557	Increased variability in muscle fiber diameter
HP:0003558	Viral infection-induced rhabdomyolysis
HP:0003559	Muscle hyperirritability
HP:0003560	Muscular dystrophy
HP:0003561	Birth length less than 3rd percentile
HP:0003562	Abnormal metaphyseal vascular invasion
HP:0003563	Decreased LDL cholesterol concentration
HP:0003564	Folate-dependent fragile site at Xq28
HP:0003565	Elevated erythrocyte sedimentation rate
HP:0003566	Increased serum prostaglandin E2
HP:0003568	Decreased glucosephosphate isomerase activity
HP:0003570	Molybdenum cofactor deficiency
HP:0003571	Propionicacidemia
HP:0003572	Low plasma citrulline
HP:0003573	Increased total bilirubin
HP:0003574	Positive regitine blocking test
HP:0003575	Increased intracellular sodium
HP:0003577	Congenital onset
HP:0003581	Adult onset
HP:0003584	Late onset
HP:0003587	Insidious onset
HP:0003593	Infantile onset
HP:0003596	Middle age onset
HP:0003606	Absent urinary urothione
HP:0003607	4-Hydroxyphenylacetic aciduria
HP:0003609	Foam cells with lamellar inclusion bodies
HP:0003610	Fibroblast metachromasia
HP:0003612	Positive ferric chloride test
HP:0003613	Antiphospholipid antibody positivity
HP:0003614	Trimethylaminuria
HP:0003616	Premature separation of centromeric heterochromatin
HP:0003621	Juvenile onset
HP:0003623	Neonatal onset
HP:0003634	Amyoplasia
HP:0003635	Loss of subcutaneous adipose tissue in limbs
HP:0003637	Reduced 4-Hydroxyphenylpyruvate dioxygenase activity
HP:0003639	Elevated urinary epinephrine
HP:0003640	Foam cells in visceral organs and CNS
HP:0003641	Hemoglobinuria
HP:0003642	Type I transferrin isoform profile
HP:0003643	Sulfite oxidase deficiency
HP:0003645	Prolonged partial thromboplastin time
HP:0003646	Bicarbonaturia
HP:0003647	Electron transfer flavoprotein-ubiquinone oxidoreductase defect
HP:0003648	Lacticaciduria
HP:0003649	Abnormality of glycoside metabolism
HP:0003651	Foam cells
HP:0003652	Recurrent myoglobinuria
HP:0003653	Cellular metachromasia
HP:0003654	Reduced dihydropyrimidine dehydrogenase activity
HP:0003655	Reduced activity of N-acetylglucosaminyltransferase II
HP:0003656	Decreased beta-glucocerebrosidase protein and activity
HP:0003657	Granular osmiophilic deposits (GROD) in cells
HP:0003658	Hypomethioninemia
HP:0003665	Amyotrophy of the musculature of the pelvis
HP:0003674	Onset
HP:0003676	Progressive
HP:0003677	Slow progression
HP:0003678	Rapidly progressive
HP:0003679	Pace of progression
HP:0003680	Nonprogressive
HP:0003682	Variable progression rate
HP:0003683	Large beaked nose
HP:0003687	Centrally nucleated skeletal muscle fibers
HP:0003688	Cytochrome C oxidase-negative muscle fibers
HP:0003689	Multiple mitochondrial DNA deletions
HP:0003690	Limb muscle weakness
HP:0003691	Scapular winging
HP:0003693	Distal amyotrophy
HP:0003694	Late-onset proximal muscle weakness
HP:0003696	Absent epiphysis of the distal phalanx of the 5th finger
HP:0003697	Scapuloperoneal amyotrophy
HP:0003698	Difficulty standing
HP:0003700	Generalized amyotrophy
HP:0003701	Proximal muscle weakness
HP:0003704	Scapuloperoneal weakness
HP:0003707	Calf muscle pseudohypertrophy
HP:0003710	Exercise-induced muscle cramps
HP:0003712	Skeletal muscle hypertrophy
HP:0003713	Muscle fiber necrosis
HP:0003715	Myofibrillar myopathy
HP:0003716	Generalized muscular appearance from birth
HP:0003717	Minimal subcutaneous fat
HP:0003719	Muscle mounding
HP:0003720	Generalized muscle hypertrophy
HP:0003722	Neck flexor weakness
HP:0003724	Shoulder girdle muscle atrophy
HP:0003725	Firm muscles
HP:0003729	Enteroviral dermatomyositis syndrome
HP:0003730	EMG: myotonic runs
HP:0003731	Quadriceps muscle weakness
HP:0003733	Thigh hypertrophy
HP:0003736	Autophagic vacuoles
HP:0003737	Mitochondrial myopathy
HP:0003738	Exercise-induced myalgia
HP:0003739	Myoclonic spasms
HP:0003740	Myotonia with warm-up phenomenon
HP:0003741	Congenital muscular dystrophy
HP:0003743	Genetic anticipation
HP:0003744	Genetic anticipation with paternal anticipation bias
HP:0003745	Sporadic
HP:0003749	Pelvic girdle muscle weakness
HP:0003750	Increased muscle fatiguability
HP:0003752	Episodic flaccid weakness
HP:0003755	Type 1 fibers relatively smaller than type 2 fibers
HP:0003756	Skeletal myopathy
HP:0003758	Reduced subcutaneous adipose tissue
HP:0003759	Hypoplasia of lymphatic vessels
HP:0003760	Percussion-induced rapid rolling muscle contractions
HP:0003761	Calcinosis
HP:0003762	Uterus didelphys
HP:0003763	Bruxism
HP:0003764	Nevus
HP:0003765	Psoriasiform dermatitis
HP:0003768	Periodic paralysis
HP:0003771	Pulp stones
HP:0003774	Stage 5 chronic kidney disease
HP:0003777	Pili torti
HP:0003778	Short mandibular rami
HP:0003779	Antegonial notching of mandible
HP:0003781	Excessive salivation
HP:0003782	Eunuchoid habitus
HP:0003783	Externally rotated/abducted legs
HP:0003784	Type 1 collagen overmodification
HP:0003785	Decreased CSF homovanillic acid
HP:0003787	Type 1 and type 2 muscle fiber minicore regions
HP:0003789	Minicore myopathy
HP:0003791	Deposits immunoreactive to beta-amyloid protein
HP:0003795	Short middle phalanx of toe
HP:0003796	Irregular iliac crest
HP:0003797	Limb-girdle muscle atrophy
HP:0003798	Nemaline bodies
HP:0003799	Marked delay in bone age
HP:0003800	Muscle abnormality related to mitochondrial dysfunction
HP:0003803	Type 1 muscle fiber predominance
HP:0003805	Rimmed vacuoles
HP:0003808	Abnormal muscle tone
HP:0003809	Reduced intrathoracic adipose tissue
HP:0003810	Late-onset distal muscle weakness
HP:0003811	Neonatal death
HP:0003812	Phenotypic variability
HP:0003819	Death in childhood
HP:0003826	Stillbirth
HP:0003828	Variable expressivity
HP:0003829	Incomplete penetrance
HP:0003831	Age-dependent penetrance
HP:0003832	Abnormality of the tibial plateaux
HP:0003833	Laterally deficient tibial plateaux
HP:0003834	Shoulder dislocation
HP:0003835	Shoulder subluxation
HP:0003836	Stippled calcification of the shoulder
HP:0003837	Soft-tissue ossification around the shoulders
HP:0003839	Abnormality of upper limb epiphysis morphology
HP:0003840	Delayed upper limb epiphyseal ossification
HP:0003841	Fragmented epiphyses of the upper limbs
HP:0003842	Irregular epiphyses of the upper limbs
HP:0003843	Round epiphyses of the upper limbs
HP:0003844	Small epiphyses of the upper limbs
HP:0003846	Wide epiphyseal plates of the upper limbs
HP:0003848	Cupped metaphyses of the upper limbs
HP:0003849	Flared upper limb metaphysis
HP:0003850	Upper-limb metaphyseal irregularity
HP:0003851	Lytic defects in metaphyses of the upper limbs
HP:0003852	Normal density transverse bands in metaphyses of the upper limbs
HP:0003853	Sclerosis with transverse striations in metaphyses of the upper limbs
HP:0003854	Sclerosis of metaphyses of the upper limbs
HP:0003855	Spurred metaphyses of the upper limbs
HP:0003856	Upper limb metaphyseal widening
HP:0003858	Cortical diaphyseal irregularity of the upper limbs
HP:0003859	Cortical diaphyseal thickening of the upper limbs
HP:0003860	Diaphyseal sclerosis of the upper limbs
HP:0003861	Broad diaphyses of the upper limbs
HP:0003862	Absent humerus
HP:0003863	Angulated humerus
HP:0003864	Bifid humerus
HP:0003865	Bowed humerus
HP:0003866	Coarse humeral trabeculae
HP:0003867	Humeral cortical irregularity
HP:0003868	Humeral cortical thickening
HP:0003869	Humeral cortical thinning
HP:0003870	Crumpled humerus
HP:0003871	Deformed humerus
HP:0003872	Humeral exostoses
HP:0003874	Humerus varus
HP:0003875	Humeral lytic defects
HP:0003876	Osteoporotic humerus
HP:0003877	Oval transradiancy of humerus
HP:0003878	Periosteal new bone of humerus
HP:0003879	Humeral pseudarthrosis
HP:0003880	Sclerotic foci of the humerus
HP:0003881	Humeral sclerosis
HP:0003882	Slender humerus
HP:0003883	Tapered humerus
HP:0003884	Triangular humerus
HP:0003885	Undermodeled humerus
HP:0003886	Wide humerus
HP:0003887	Abnormality of the humeral heads
HP:0003888	Flattened humeral heads
HP:0003889	Abnormality of the deltoid tuberosities
HP:0003890	Prominent deltoid tuberosities
HP:0003891	Abnormality of the humeral epiphysis
HP:0003892	Absent humeral epiphyseal ossification
HP:0003893	Advanced ossification of the humeral epiphysis
HP:0003894	Delayed humeral epiphyseal ossification
HP:0003895	Flattened humeral epiphyses
HP:0003896	Irregular humeral epiphyses
HP:0003897	Irregular ossification of the humeral epiphyses
HP:0003898	Large humeral epiphyses
HP:0003899	Round humeral epiphyses
HP:0003900	Small humeral epiphyses
HP:0003901	Stippled calcification of the humeral epiphyses
HP:0003902	Epiphyseal stippling of the humerus
HP:0003903	Broad humeral epiphyses
HP:0003904	Wide epiphyses of the upper limbs
HP:0003905	Abnormality of the humeral epiphyseal plate
HP:0003906	Broad humeral epiphyseal plate
HP:0003907	Abnormality of the humeral metaphyses
HP:0003908	Corner fracture of metaphysis
HP:0003909	Cortical subperiosteal resorption of humeral metaphyses
HP:0003910	Enlarged humeral metaphyses
HP:0003911	Flared humeral metaphysis
HP:0003912	Frayed humeral metaphyses
HP:0003913	Humeral metaphyseal irregularity
HP:0003914	Irregular ossification of humeral metaphyses
HP:0003915	Lytic defects of the humeral metaphysis
HP:0003916	Normal-density transverse humeral bands
HP:0003917	Pointed humeral metaphysis
HP:0003918	Sclerotic humeral metaphysis
HP:0003919	Sclerotic humeral metaphysis with longitudinal striations
HP:0003920	Sloping humeral metaphysis
HP:0003921	Laterally sloping humeral metaphysis
HP:0003922	Spurred humeral metaphysis
HP:0003923	Square humeral metaphysis
HP:0003924	Stippled calcification of humeral metaphysis
HP:0003926	Abnormality of the humeral diaphysis
HP:0003927	Cortical irregularity of humeral diaphysis
HP:0003928	Cortical thickening of humeral diaphysis
HP:0003929	Ground glass opacity of humeral diaphysis
HP:0003930	Lytic defects of humeral diaphysis
HP:0003931	Periosteal new bone of humeral diaphysis
HP:0003932	Sclerotic foci of humeral diaphysis
HP:0003933	Sclerosis of humeral diaphysis
HP:0003934	Slender humeral diaphysis
HP:0003935	Wide humeral diaphysis
HP:0003938	Synostosis involving the elbow
HP:0003939	Humeroulnar synostosis
HP:0003940	Osteoarthritis of the elbow
HP:0003941	Stippled calcification of the elbow
HP:0003942	Synovial chondromatosis of the elbow
HP:0003943	Abnormality of the joint spaces of the elbow
HP:0003944	Narrow joint spaces of the elbow
HP:0003945	Irregular articular surfaces of the elbow joints
HP:0003946	Abnormality of the epiphyses of the elbow
HP:0003947	Delayed elbow epiphyseal ossification
HP:0003948	Irregular epiphyses of the elbow
HP:0003949	Abnormality of the elbow metaphyses
HP:0003950	Flared elbow metaphyses
HP:0003951	Distal humeral metaphyseal irregularity
HP:0003952	Sclerotic foci of metaphyses of the elbow
HP:0003953	Absent forearm bone
HP:0003954	Angulated forearm bones
HP:0003955	Bone-in-a-bone appearance of forearm
HP:0003956	Bowed forearm bones
HP:0003957	Cortical thickening of the forearm bones
HP:0003958	Cross-fusion of the forearm bones
HP:0003959	Deformed forearm bones
HP:0003960	Exostoses of the forearm bones
HP:0003961	Fractured forearm bones
HP:0003963	Lytic defects of the forearm bones
HP:0003964	Osteoporotic forearm bones
HP:0003965	Pseudarthrosis of the forearm bones
HP:0003966	Sclerotic foci in forearm bones
HP:0003967	Sclerotic forearm bones
HP:0003969	Slender forearm bones
HP:0003970	Undermodelled forearm bones
HP:0003971	Broad forearm bones
HP:0003973	Wide radioulnar joints
HP:0003974	Absent radius
HP:0003975	obsolete Chevron-shaped/cone-shaped radius
HP:0003976	Constricted radius
HP:0003977	Deformed radius
HP:0003978	Fractured radius
HP:0003979	Lytic defects of the radius
HP:0003980	Pseudarthrosis of the radius
HP:0003981	Broad radius
HP:0003982	Aplasia of the ulna
HP:0003984	Posteriorly dislocated ulna
HP:0003985	Exostoses of the ulna
HP:0003986	Exostoses of the radius
HP:0003987	Fractured ulna
HP:0003988	Long ulna
HP:0003989	Notched ulna
HP:0003990	Pointed ulna
HP:0003991	Osteosclerosis of the ulna
HP:0003992	Slender ulna
HP:0003993	Broad ulna
HP:0003994	Dislocated wrist
HP:0003995	Abnormality of the radial head
HP:0003996	Flattened radial head
HP:0003997	Hypoplastic radial head
HP:0003998	Constricted radial neck
HP:0003999	Abnormality of radial epiphyses
HP:0004000	Cone-shaped distal radial epiphysis
HP:0004001	Medially deficient radial epiphyses
HP:0004002	Flattened radial epiphyses
HP:0004003	Medially flattened radial epiphyses
HP:0004004	Irregular radial epiphyses
HP:0004005	Large radial epiphyses
HP:0004006	Round radial epiphyses
HP:0004007	Sclerotic radial epiphyses
HP:0004008	Sloping radial epiphyses
HP:0004009	Medially sloping radial epiphyses
HP:0004010	Small radial epiphyses
HP:0004012	Premature fusion of the radial epiphyseal plates
HP:0004013	Medially fused radial epiphyseal plates
HP:0004014	Broad radial epiphyseal plate
HP:0004015	Abnormality of radial metaphyses
HP:0004016	Cupped radial metaphyses
HP:0004017	Exostoses of the radial metaphysis
HP:0004018	Flared radial metaphysis
HP:0004019	Radial metaphyseal irregularity
HP:0004020	Irregular ossification of the radial metaphysis
HP:0004021	Lytic defects of radial metaphysis
HP:0004022	Sclerotic radial metaphysis with longitudinal striations
HP:0004023	Sloping radial metaphysis
HP:0004024	Medially sloping radial metaphysis
HP:0004025	Spurred radial metaphysis
HP:0004026	Broad radial metaphysis
HP:0004027	Abnormality of radial diaphysis
HP:0004028	Spurs of radial diaphysis
HP:0004029	Lytic defects of radial diaphysis
HP:0004030	Patchy sclerosis of radial diaphysis
HP:0004031	Broad radial diaphysis
HP:0004032	Abnormality of the olecranon
HP:0004033	Curved olecranon
HP:0004034	Irregular olecranon
HP:0004035	Abnormality of the styloid process of ulna
HP:0004036	Long styloid process of ulna
HP:0004037	Abnormality of the ulnar epiphyses
HP:0004038	Bony spikule of ulnar epiphyseal plate
HP:0004039	Abnormality of ulnar metaphysis
HP:0004040	Corner fragments of ulnar metaphysis
HP:0004041	Cupped ulnar metaphysis
HP:0004042	Ulnar metaphyseal irregularity
HP:0004043	Lytic defects of ulnar metaphysis
HP:0004044	Pointed ulnar metaphysis
HP:0004045	Sloping ulnar metaphysis
HP:0004046	Spurred ulnar metaphysis
HP:0004047	Wide ulnar metaphysis
HP:0004048	Narrow joint spaces of wrist
HP:0004049	Decreased carpal angles of wrist
HP:0004050	Absent hand
HP:0004051	Advanced ossification of the hand bones
HP:0004052	Delayed ossification of the hand bones
HP:0004053	Dysharmonic maturation of the hand bones
HP:0004054	Sclerosis of hand bone
HP:0004057	Mitten deformity
HP:0004058	Hand monodactyly
HP:0004059	Radial club hand
HP:0004060	Trident hand
HP:0004066	obsolete Laterally deviated thumb phalanges
HP:0004083	obsolete Laterally deviated terminal thumb phalanx
HP:0004090	obsolete Advanced maturation/advanced ossification of terminal thumb phalanx epiphysis
HP:0004095	Curved fingers
HP:0004097	Deviation of finger
HP:0004099	Macrodactyly
HP:0004100	Abnormal 2nd finger morphology
HP:0004110	obsolete Radially deviated index finger phalanges
HP:0004112	Midline nasal groove
HP:0004121	obsolete Radially displaced proximal index finger phalanx
HP:0004122	Midline defect of the nose
HP:0004132	Dimple on nasal tip
HP:0004138	obsolete Metaphyseal abnormality of middle phalanx of the 2nd finger
HP:0004139	obsolete Flared metaphysis of middle phalanx of index finger
HP:0004143	obsolete Radially deviated terminal index finger phalanx
HP:0004144	obsolete Duplication of terminal index finger phalanx
HP:0004150	Abnormal 3rd finger morphology
HP:0004153	obsolete Overgrowth of middle finger
HP:0004157	obsolete Accessory middle-finger phalanges
HP:0004161	obsolete Periosteal new bone of middle finger phalanges
HP:0004162	obsolete Radially pointed middle finger phalanges
HP:0004168	obsolete Radially pointed proximal middle-finger phalanx
HP:0004172	Abnormality of the middle phalanx of the 3rd finger
HP:0004174	obsolete Accessory middle phalanx of middle finger
HP:0004175	obsolete Periosteal new bone of middle phalanx of middle-finger
HP:0004180	Short distal phalanx of the 3rd finger
HP:0004183	obsolete Abnormality of the epiphyses of the terminal phalanx of the middle finger
HP:0004184	obsolete Cone-shaped epiphysis of terminal phalanx of the middle finger
HP:0004185	obsolete Fused epiphysis of terminal phalanx of the middle finger
HP:0004186	obsolete Large epiphysis of terminal phalanx of the middle finger
HP:0004187	obsolete Prematurely fused epiphysis of terminal phalanx of the middle finger
HP:0004188	Abnormal 4th finger morphology
HP:0004192	obsolete Bracket epiphyses of the 4th finger
HP:0004193	obsolete Expanded phalanges of the ring finger
HP:0004194	obsolete Hypoplastic phalanges of the ring finger
HP:0004195	Osteolytic defects of the phalanges of the 4th finger
HP:0004196	obsolete Short phalanges of the ring finger
HP:0004197	Symphalangism of the 4th finger
HP:0004198	obsolete Wide/broad phalanges of the ring finger
HP:0004201	obsolete Expanded proximal phalanx of the ring finger
HP:0004202	obsolete Lytic defects of the proximal phalanx of the ring finger
HP:0004203	obsolete Short proximal phalanx of the ring finger
HP:0004207	Abnormal 5th finger morphology
HP:0004209	Clinodactyly of the 5th finger
HP:0004213	Abnormal 5th finger phalanx morphology
HP:0004214	Curved phalanges of the 5th finger
HP:0004216	Osteolytic defects of the phalanges of the 5th finger
HP:0004218	Symphalangism of the 5th finger
HP:0004219	Abnormality of the middle phalanx of the 5th finger
HP:0004220	Short middle phalanx of the 5th finger
HP:0004222	Cone-shaped epiphysis of the distal phalanx of the 5th finger
HP:0004223	Ivory epiphysis of the distal phalanx of the 5th finger
HP:0004224	Abnormality of the epiphysis of the middle phalanx of the 5th finger
HP:0004225	Abnormality of the distal phalanx of the 5th finger
HP:0004226	Curved distal phalanx of the 5th finger
HP:0004227	Short distal phalanx of the 5th finger
HP:0004230	Subluxation of the proximal interphalangeal joint of the little finger
HP:0004231	Carpal bone aplasia
HP:0004232	Accessory carpal bones
HP:0004233	Advanced ossification of carpal bones
HP:0004234	Bone-in-a-bone appearance of carpal bones
HP:0004235	Comma-shaped carpal bones
HP:0004236	Irregular carpal bones
HP:0004237	Large carpal bones
HP:0004238	Lytic defects of carpal bones
HP:0004239	Proximally placed carpal bones
HP:0004240	Sclerotic foci within carpal bones
HP:0004241	Stippled calcification in carpal bones
HP:0004242	Broad carpal bones
HP:0004243	Abnormality of the scaphoid
HP:0004244	Accessory scaphoid
HP:0004245	Comma-shaped scaphoid
HP:0004246	Delayed ossification of the scaphoid
HP:0004247	Small scaphoid
HP:0004248	Abnormality of the lunate bone
HP:0004249	Accessory lunate
HP:0004250	Proximally placed lunate
HP:0004251	Lunate-triquetral fusion
HP:0004252	Abnormality of the trapezium
HP:0004253	Absent trapezium
HP:0004254	Delayed ossification of the trapezium
HP:0004255	Small trapezium
HP:0004256	Abnormality of the trapezoid bone
HP:0004257	Delayed ossification of the trapezoid bone
HP:0004258	Small trapezoid bone
HP:0004259	Abnormality of the hamate bone
HP:0004260	Large hamate bone
HP:0004261	Wide hamate bone
HP:0004262	Abnormality of the capitate bone
HP:0004263	Large capitate bone
HP:0004264	Narrow carpal joint spaces
HP:0004267	Narrow small joints of the hand
HP:0004268	Osteoarthritis of the small joints of the hand
HP:0004269	Subluxation of the small joints of the hand
HP:0004271	Cortical thickening of hand bones
HP:0004272	Cortical thinning of hand bones
HP:0004273	Cupped metaphyses of hand bones
HP:0004274	Deficient ossification of hand bones
HP:0004275	Duplication of hand bones
HP:0004276	Exostoses of hand bones
HP:0004277	Fractured hand bones
HP:0004278	Synostosis involving bones of the hand
HP:0004279	Short palm
HP:0004280	Irregular ossification of hand bones
HP:0004281	Irregular sclerosis of hand bones
HP:0004283	Narrow palm
HP:0004284	Notched hand bones
HP:0004285	Overmodelled hand bones
HP:0004286	Patchy sclerosis of hand bones
HP:0004287	Pointed hand bones
HP:0004288	Pseudoepiphyses of hand bones
HP:0004289	Sclerotic foci in hand bones
HP:0004290	Sclerosis of hand bones with transverse striations
HP:0004291	Stippled calcification of hand bones
HP:0004292	Undermodelled hand bones
HP:0004293	Synostosis of second metacarpal-trapezoid
HP:0004294	Subluxation of metacarpal phalangeal joints
HP:0004295	Abnormality of the gastric mucosa
HP:0004296	Abnormality of gastrointestinal vasculature
HP:0004297	Abnormality of the biliary system
HP:0004298	Abnormality of the abdominal wall
HP:0004299	Hernia of the abdominal wall
HP:0004302	Functional motor deficit
HP:0004303	Abnormality of muscle fibers
HP:0004305	Involuntary movements
HP:0004306	Abnormal endocardium morphology
HP:0004307	Abnormal anatomic location of the heart
HP:0004308	Ventricular arrhythmia
HP:0004309	Ventricular preexcitation
HP:0004311	Abnormal macrophage morphology
HP:0004312	Abnormality of reticulocytes
HP:0004313	Decreased antibody level in blood
HP:0004315	Decreased circulating IgG level
HP:0004319	Decreased circulating aldosterone level
HP:0004320	Vaginal fistula
HP:0004321	Bladder fistula
HP:0004322	Short stature
HP:0004323	Abnormality of body weight
HP:0004324	Increased body weight
HP:0004325	Decreased body weight
HP:0004326	Cachexia
HP:0004327	Abnormal vitreous humor morphology
HP:0004328	Abnormal anterior eye segment morphology
HP:0004329	Abnormal posterior eye segment morphology
HP:0004330	Increased skull ossification
HP:0004331	Decreased skull ossification
HP:0004332	Abnormal lymphocyte morphology
HP:0004333	Bone-marrow foam cells
HP:0004334	Dermal atrophy
HP:0004336	Myelin outfoldings
HP:0004337	Abnormality of amino acid metabolism
HP:0004338	Abnormality of aromatic amino acid family metabolism
HP:0004339	Abnormality of sulfur amino acid metabolism
HP:0004340	Abnormality of vitamin B metabolism
HP:0004341	Abnormality of vitamin B12 metabolism
HP:0004342	Abnormality of galactoside metabolism
HP:0004343	Abnormality of glycosphingolipid metabolism
HP:0004344	Abnormality of cerebrosidase metabolism
HP:0004345	Abnormality of ganglioside metabolism
HP:0004347	Weakness of muscles of respiration
HP:0004348	Abnormality of bone mineral density
HP:0004349	Reduced bone mineral density
HP:0004352	Abnormality of purine metabolism
HP:0004353	Abnormality of pyrimidine metabolism
HP:0004354	Abnormality of carboxylic acid metabolism
HP:0004355	Abnormality of proteoglycan metabolism
HP:0004356	Abnormality of lysosomal metabolism
HP:0004357	Abnormality of leucine metabolism
HP:0004358	Abnormality of superoxide metabolism
HP:0004359	Abnormality of fatty-acid metabolism
HP:0004360	Abnormality of acid-base homeostasis
HP:0004361	Abnormality of circulating leptin level
HP:0004362	Abnormality of enteric ganglion morphology
HP:0004363	Abnormality of calcium homeostasis
HP:0004364	Abnormality of nitrogen compound homeostasis
HP:0004365	Abnormality of tryptophan metabolism
HP:0004366	Abnormality of glycolysis
HP:0004367	Abnormality of glycoprotein metabolism
HP:0004368	Increased purine level
HP:0004369	Decreased purine level
HP:0004370	Abnormality of temperature regulation
HP:0004371	Abnormality of glycosaminoglycan metabolism
HP:0004372	Reduced consciousness/confusion
HP:0004373	Focal dystonia
HP:0004374	Hemiplegia/hemiparesis
HP:0004375	Neoplasm of the nervous system
HP:0004376	Neuroblastic tumors
HP:0004377	Hematological neoplasm
HP:0004378	Abnormality of the anus
HP:0004379	Abnormality of alkaline phosphatase activity
HP:0004380	Aortic valve calcification
HP:0004381	Supravalvular aortic stenosis
HP:0004382	Mitral valve calcification
HP:0004383	Hypoplastic left heart
HP:0004384	Type I truncus arteriosus
HP:0004385	Protracted diarrhea
HP:0004386	Gastrointestinal inflammation
HP:0004387	Enterocolitis
HP:0004388	Microcolon
HP:0004389	Intestinal pseudo-obstruction
HP:0004390	Hamartomatous polyposis
HP:0004392	Prune belly
HP:0004394	Multiple gastric polyps
HP:0004395	Malnutrition
HP:0004396	Poor appetite
HP:0004397	Ectopic anus
HP:0004398	Peptic ulcer
HP:0004399	Congenital pyloric atresia
HP:0004400	Abnormality of the pylorus
HP:0004401	Meconium ileus
HP:0004403	Proximal esophageal atresia
HP:0004404	Abnormal nipple morphology
HP:0004405	Prominent nipples
HP:0004406	Spontaneous, recurrent epistaxis
HP:0004407	Bony paranasal bossing
HP:0004408	Abnormality of the sense of smell
HP:0004409	Hyposmia
HP:0004411	Deviated nasal septum
HP:0004414	Abnormality of the pulmonary artery
HP:0004415	Pulmonary artery stenosis
HP:0004416	Precocious atherosclerosis
HP:0004417	Intermittent claudication
HP:0004418	Thrombophlebitis
HP:0004419	Recurrent thrombophlebitis
HP:0004420	Arterial thrombosis
HP:0004421	Elevated systolic blood pressure
HP:0004422	Biparietal narrowing
HP:0004423	Cranium bifidum occultum
HP:0004425	Flat forehead
HP:0004426	Abnormality of the cheek
HP:0004428	Elfin facies
HP:0004429	Recurrent viral infections
HP:0004430	Severe combined immunodeficiency
HP:0004431	Complement deficiency
HP:0004432	Agammaglobulinemia
HP:0004433	Secretory IgA deficiency
HP:0004434	C8 deficiency
HP:0004437	Cranial hyperostosis
HP:0004438	Hyperostosis frontalis interna
HP:0004439	Craniofacial dysostosis
HP:0004440	Coronal craniosynostosis
HP:0004442	Sagittal craniosynostosis
HP:0004443	Lambdoidal craniosynostosis
HP:0004444	Spherocytosis
HP:0004445	Elliptocytosis
HP:0004446	Stomatocytosis
HP:0004447	Poikilocytosis
HP:0004448	Fulminant hepatic failure
HP:0004450	Preauricular skin furrow
HP:0004451	Postauricular skin tag
HP:0004452	Abnormality of the middle ear ossicles
HP:0004453	Overfolding of the superior helices
HP:0004454	Abnormal middle ear reflexes
HP:0004458	Dilatated internal auditory canal
HP:0004459	Exostosis of the external auditory canal
HP:0004461	Congenital earlobe sinuses
HP:0004463	Absent brainstem auditory responses
HP:0004464	Postauricular pit
HP:0004466	Prolonged brainstem auditory evoked potentials
HP:0004467	Preauricular pit
HP:0004468	Anomalous tracheal cartilage
HP:0004469	Chronic bronchitis
HP:0004470	Atretic occipital cephalocele
HP:0004471	Aplasia cutis congenita over the scalp vertex
HP:0004472	Mandibular hyperostosis
HP:0004474	Persistent open anterior fontanelle
HP:0004476	Aplasia cutis congenita over parietal area
HP:0004478	Ethmoidal encephalocele
HP:0004481	Progressive macrocephaly
HP:0004482	Relative macrocephaly
HP:0004484	Craniofacial asymmetry
HP:0004485	Cessation of head growth
HP:0004487	Acrobrachycephaly
HP:0004488	Macrocephaly at birth
HP:0004490	Calvarial hyperostosis
HP:0004491	Large posterior fontanelle
HP:0004492	Widely patent fontanelles and sutures
HP:0004493	Craniofacial hyperostosis
HP:0004495	Thin anteverted nares
HP:0004496	Posterior choanal atresia
HP:0004499	Chronic rhinitis due to narrow nasal airway
HP:0004502	Bilateral choanal atresia
HP:0004510	Pancreatic islet-cell hyperplasia
HP:0004523	Long eyebrows
HP:0004524	Temporal hypotrichosis
HP:0004527	Large clumps of pigment irregularly distributed along hair shaft
HP:0004528	Generalized hypotrichosis
HP:0004529	Atrophic, patchy alopecia
HP:0004532	Sacral hypertrichosis
HP:0004535	Anterior cervical hypertrichosis
HP:0004540	Congenital, generalized hypertrichosis
HP:0004544	Pointed frontal hairline
HP:0004552	Scarring alopecia of scalp
HP:0004554	Generalized hypertrichosis
HP:0004557	Anterior vertebral fusion
HP:0004558	Cervical platyspondyly
HP:0004562	Beaking of vertebral bodies T12-L3
HP:0004563	Increased spinal bone density
HP:0004565	Severe platyspondyly
HP:0004566	Pear-shaped vertebrae
HP:0004568	Beaking of vertebral bodies
HP:0004570	Increased vertebral height
HP:0004571	Widening of cervical spinal canal
HP:0004573	Anterior wedging of T11
HP:0004575	Fusion of midcervical facet joints
HP:0004576	Sclerotic vertebral endplates
HP:0004580	Anterior scalloping of vertebral bodies
HP:0004581	Increased anterior vertebral height
HP:0004582	Irregularity of vertebral bodies
HP:0004586	Biconcave vertebral bodies
HP:0004589	Dysplasia of second lumbar vertebra
HP:0004590	Hypoplastic sacrum
HP:0004591	Disc-like vertebral bodies
HP:0004592	Thoracic platyspondyly
HP:0004594	Hump-shaped mound of bone in central and posterior portions of vertebral endplate
HP:0004598	Supernumerary vertebral ossification centers
HP:0004599	Absent or minimally ossified vertebral bodies
HP:0004601	Spina bifida occulta at L5
HP:0004602	Cervical C2/C3 vertebral fusion
HP:0004603	Hyperconvex vertebral body endplates
HP:0004605	Absent vertebral body mineralization
HP:0004606	Unossified vertebral bodies
HP:0004607	Anterior beaking of lower thoracic vertebrae
HP:0004608	Anteriorly placed odontoid process
HP:0004609	Patchy distortion of vertebrae
HP:0004610	Lumbar spinal canal stenosis
HP:0004611	Anterior concavity of thoracic vertebrae
HP:0004614	Spina bifida occulta at S1
HP:0004616	Cleft vertebral arch
HP:0004617	Butterfly vertebral arch
HP:0004618	Sandwich appearance of vertebral bodies
HP:0004619	Lumbar kyphoscoliosis
HP:0004621	Enlarged vertebral pedicles
HP:0004622	Progressive intervertebral space narrowing
HP:0004625	Biconvex vertebral bodies
HP:0004626	Lumbar scoliosis
HP:0004629	Small cervical vertebral bodies
HP:0004630	Anterior beaking of thoracic vertebrae
HP:0004631	Decreased cervical spine flexion due to contractures of posterior cervical muscles
HP:0004632	Cervical segmentation defect
HP:0004633	Lower thoracic kyphosis
HP:0004634	Cuboid-shaped vertebral bodies
HP:0004635	Cervical C5/C6 vertebrae fusion
HP:0004637	Decreased cervical spine mobility
HP:0004639	Elevated amniotic fluid alpha-fetoprotein
HP:0004646	Hypoplasia of the nasal bone
HP:0004660	Hypoplasia of facial musculature
HP:0004661	Frontalis muscle weakness
HP:0004664	Facial midline hemangioma
HP:0004673	Decreased facial expression
HP:0004676	Prominent supraorbital arches in adult
HP:0004679	Large tarsal bones
HP:0004681	Deep longitudinal plantar crease
HP:0004684	Talipes valgus
HP:0004686	Short third metatarsal
HP:0004688	Irregular tarsal bones
HP:0004689	Short fourth metatarsal
HP:0004690	Thickened Achilles tendon
HP:0004691	2-3 toe syndactyly
HP:0004692	4-5 toe syndactyly
HP:0004695	Calcaneal epiphyseal stippling
HP:0004696	Talipes cavus equinovarus
HP:0004699	Osteoporotic metatarsal
HP:0004704	Short fifth metatarsal
HP:0004712	Renal malrotation
HP:0004713	Reversible renal failure
HP:0004717	Axial malrotation of the kidney
HP:0004719	Hyperechogenic kidneys
HP:0004722	Thickening of the glomerular basement membrane
HP:0004724	Calcium nephrolithiasis
HP:0004727	Impaired renal concentrating ability
HP:0004729	Acute tubulointerstitial nephritis
HP:0004732	Impaired renal uric acid clearance
HP:0004734	Renal cortical microcysts
HP:0004736	Crossed fused renal ectopia
HP:0004737	Global glomerulosclerosis
HP:0004742	Abnormality of the renal collecting system
HP:0004743	Chronic tubulointerstitial nephritis
HP:0004746	Glomerular subendothelial electron-dense deposits
HP:0004749	Atrial flutter
HP:0004751	Paroxysmal ventricular tachycardia
HP:0004752	Congenital atrioventricular dissociation
HP:0004754	Permanent atrial fibrillation
HP:0004755	Supraventricular tachycardia
HP:0004756	Ventricular tachycardia
HP:0004757	Paroxysmal atrial fibrillation
HP:0004758	Effort-induced polymorphic ventricular tachycardias
HP:0004759	obsolete Nodular calcific aortic valve disease
HP:0004760	obsolete Congenital septal defect
HP:0004761	Post-angioplasty coronary artery restenosis
HP:0004762	Hypoplasia of right ventricle
HP:0004763	Paroxysmal supraventricular tachycardia
HP:0004764	Myxomatous mitral valve degeneration
HP:0004768	Sparse anterior scalp hair
HP:0004771	Premature graying of body hair
HP:0004779	Brittle scalp hair
HP:0004780	Elbow hypertrichosis
HP:0004782	Hypotrichosis of the scalp
HP:0004783	Duodenal polyposis
HP:0004784	Juvenile gastrointestinal polyposis
HP:0004785	Malrotation of colon
HP:0004786	Jejunal diverticula
HP:0004787	Fulminant hepatitis
HP:0004788	Intestinal lymphedema
HP:0004789	Lactose intolerance
HP:0004790	Hypoplasia of the small intestine
HP:0004791	Esophageal ulceration
HP:0004792	Rectoperineal fistula
HP:0004794	Malrotation of small bowel
HP:0004795	Hamartomatous stomach polyps
HP:0004796	Gastrointestinal obstruction
HP:0004797	Multiple small bowel atresias
HP:0004798	Recurrent infection of the gastrointestinal tract
HP:0004799	Jejunoileal diverticula
HP:0004800	Duodenal diverticula
HP:0004802	Episodic hemolytic anemia
HP:0004804	Congenital hemolytic anemia
HP:0004808	Acute myeloid leukemia
HP:0004809	Neonatal alloimmune thrombocytopenia
HP:0004810	Congenital hypoplastic anemia
HP:0004812	B Acute Lymphoblastic Leukemia
HP:0004813	Post-transfusion thrombocytopenia
HP:0004814	Fava bean-induced hemolytic anemia
HP:0004817	Drug-sensitive hemolytic anemia
HP:0004818	Paroxysmal nocturnal hemoglobinuria
HP:0004819	Normocytic hypoplastic anemia
HP:0004820	Acute myelomonocytic leukemia
HP:0004821	Hypersegmentation of neutrophil nuclei
HP:0004822	Atypical elliptocytosis
HP:0004823	Anisopoikilocytosis
HP:0004825	Increased hemoglobin oxygen affinity
HP:0004826	Folate-unresponsive megaloblastic anemia
HP:0004828	Refractory anemia with ringed sideroblasts
HP:0004831	Recurrent thromboembolism
HP:0004835	Microspherocytosis
HP:0004836	Acute promyelocytic leukemia
HP:0004839	Pyropoikilocytosis
HP:0004840	Hypochromic microcytic anemia
HP:0004841	Reduced factor XII activity
HP:0004844	Coombs-positive hemolytic anemia
HP:0004845	Acute monocytic leukemia
HP:0004846	Prolonged bleeding after surgery
HP:0004848	Ph-positive acute lymphoblastic leukemia
HP:0004850	Recurrent deep vein thrombosis
HP:0004851	Folate-responsive megaloblastic anemia
HP:0004852	Reduced leukocyte alkaline phosphatase
HP:0004854	Intermittent thrombocytopenia
HP:0004855	Reduced protein S activity
HP:0004856	Normochromic microcytic anemia
HP:0004857	Hyperchromic macrocytic anemia
HP:0004859	Amegakaryocytic thrombocytopenia
HP:0004860	Thiamine-responsive megaloblastic anemia
HP:0004861	Refractory macrocytic anemia
HP:0004863	Compensated hemolytic anemia
HP:0004864	Refractory sideroblastic anemia
HP:0004866	Impaired ADP-induced platelet aggregation
HP:0004870	Chronic hemolytic anemia
HP:0004871	Perineal fistula
HP:0004872	Incisional hernia
HP:0004875	Neonatal inspiratory stridor
HP:0004876	Spontaneous neonatal pneumothorax
HP:0004878	Intercostal muscle weakness
HP:0004879	Intermittent hyperventilation
HP:0004880	Respiratory infections in early life
HP:0004881	Episodic hypoventilation
HP:0004885	Episodic respiratory distress
HP:0004886	Congenital laryngeal stridor
HP:0004887	Respiratory failure requiring assisted ventilation
HP:0004889	Intermittent episodes of respiratory insufficiency due to muscle weakness
HP:0004890	Elevated pulmonary artery pressure
HP:0004891	Recurrent infections due to aspiration
HP:0004894	Laryngotracheal stenosis
HP:0004897	Stress/infection-induced lactic acidosis
HP:0004898	Persistent lactic acidosis
HP:0004900	Severe lactic acidosis
HP:0004901	Exercise-induced lactic acidemia
HP:0004902	Congenital lactic acidosis
HP:0004904	Maturity-onset diabetes of the young
HP:0004905	Vitamin A deficiency
HP:0004906	Hypernatremic dehydration
HP:0004909	Hypokalemic hypochloremic metabolic alkalosis
HP:0004910	Bicarbonate-wasting renal tubular acidosis
HP:0004911	Episodic metabolic acidosis
HP:0004912	Hypophosphatemic rickets
HP:0004913	Intermittent lactic acidemia
HP:0004914	Recurrent infantile hypoglycemia
HP:0004915	Impairment of galactose metabolism
HP:0004916	Generalized distal tubular acidosis
HP:0004918	Hyperchloremic metabolic acidosis
HP:0004919	Galactose intolerance
HP:0004920	Phenylpyruvic acidemia
HP:0004921	Abnormal magnesium concentration
HP:0004922	Atypical hyperphenylalaninemia
HP:0004923	Hyperphenylalaninemia
HP:0004924	Abnormal oral glucose tolerance
HP:0004925	Chronic lactic acidosis
HP:0004926	Orthostatic hypotension due to autonomic dysfunction
HP:0004927	Pulmonary artery dilatation
HP:0004928	obsolete Peripheral arterial stenosis
HP:0004929	obsolete Coronary atherosclerosis
HP:0004930	Abnormality of the pulmonary vasculature
HP:0004931	Arteriosclerosis of small cerebral arteries
HP:0004933	Ascending aortic dissection
HP:0004934	Vascular calcification
HP:0004935	Pulmonary artery atresia
HP:0004936	Venous thrombosis
HP:0004937	Pulmonary artery aneurysm
HP:0004938	Tortuous cerebral arteries
HP:0004940	Generalized arterial calcification
HP:0004941	Extrahepatic portal hypertension
HP:0004942	Aortic aneurysm
HP:0004943	Accelerated atherosclerosis
HP:0004944	Dilatation of the cerebral artery
HP:0004945	Extracranial internal carotid artery dissection
HP:0004947	Arteriovenous fistula
HP:0004948	Vascular tortuosity
HP:0004950	Peripheral arterial stenosis
HP:0004952	Pulmonary arteriovenous fistulas
HP:0004953	obsolete Dilatation of abdominal aorta
HP:0004954	obsolete Dilatation of the descending aorta
HP:0004955	Generalized arterial tortuosity
HP:0004959	Descending thoracic aorta aneurysm
HP:0004960	Absent pulmonary artery
HP:0004961	Pulmonary artery sling
HP:0004962	Thoracic aorta calcification
HP:0004963	Calcification of the aorta
HP:0004964	Pulmonary arterial medial hypertrophy
HP:0004966	Medial calcification of large arteries
HP:0004968	Recurrent cerebral hemorrhage
HP:0004969	Peripheral pulmonary artery stenosis
HP:0004970	Ascending tubular aorta aneurysm
HP:0004971	Pulmonary artery hypoplasia
HP:0004972	Elevated mean arterial pressure
HP:0004974	Coarctation of abdominal aorta
HP:0004975	Erlenmeyer flask deformity of the femurs
HP:0004976	Knee dislocation
HP:0004977	Bilateral radial aplasia
HP:0004979	Metaphyseal sclerosis
HP:0004980	Metaphyseal rarefaction
HP:0004981	Prominent styloid process of ulna
HP:0004986	obsolete Rudimentary to absent fibulae
HP:0004987	Mesomelic leg shortening
HP:0004990	Epiphyseal streaking
HP:0004991	Rhizomelic arm shortening
HP:0004993	Slender long bones with narrow diaphyses
HP:0004997	Multicentric ossification of proximal humeral epiphyses
HP:0005001	Recurrent patellar dislocation
HP:0005003	Aplasia/Hypoplasia of the capital femoral epiphysis
HP:0005004	Flattened proximal radial epiphyses
HP:0005005	Femoral bowing present at birth, straightening with time
HP:0005008	Large joint dislocations
HP:0005009	Dumbbell-shaped humerus
HP:0005010	Osteomyelitis leading to amputation due to slow healing fractures
HP:0005011	Mesomelic arm shortening
HP:0005013	Dysplastic distal radial epiphyses
HP:0005017	Polyarticular chondrocalcinosis
HP:0005019	Diaphyseal thickening
HP:0005021	Bilateral elbow dislocations
HP:0005025	Hypoplastic distal humeri
HP:0005026	Mesomelic/rhizomelic limb shortening
HP:0005028	Widened proximal tibial metaphyses
HP:0005033	Distal ulnar hypoplasia
HP:0005035	Shortening of all phalanges of the toes
HP:0005036	Unilateral ulnar hypoplasia
HP:0005037	Proximal radio-ulnar synostosis
HP:0005039	Multiple long-bone exostoses
HP:0005041	Irregular capital femoral epiphysis
HP:0005042	Irregular, rachitic-like metaphyses
HP:0005043	Proximal humeral metaphyseal irregularity
HP:0005045	Diaphyseal cortical sclerosis
HP:0005048	Synostosis of carpal bones
HP:0005050	Anterolateral radial head dislocation
HP:0005054	Metaphyseal spurs
HP:0005059	Arthralgia/arthritis
HP:0005060	Limited elbow flexion/extension
HP:0005063	Fragmented, irregular epiphyses
HP:0005066	Cone-shaped epiphyses fused within their metaphyses
HP:0005067	Proximal fibular overgrowth
HP:0005068	Absent styloid process of ulna
HP:0005069	Rhizo-meso-acromelic limb shortening
HP:0005070	Proximal radial head dislocation
HP:0005072	Hyperextensibility at wrists
HP:0005084	Anterior radial head dislocation
HP:0005085	Limited knee flexion/extension
HP:0005086	Knee osteoarthritis
HP:0005089	Abnormal metaphyseal trabeculation
HP:0005090	Lateral femoral bowing
HP:0005092	Streaky metaphyseal sclerosis
HP:0005093	Absent proximal radial epiphyses
HP:0005096	Distal femoral bowing
HP:0005099	Severe hydrops fetalis
HP:0005100	Premature birth following premature rupture of fetal membranes
HP:0005101	High-frequency hearing impairment
HP:0005102	Cochlear degeneration
HP:0005103	Calcification of the auricular cartilage
HP:0005104	Hypoplastic nasal septum
HP:0005105	Abnormal nasal morphology
HP:0005106	Abnormality of the vertebral endplates
HP:0005107	Abnormal sacrum morphology
HP:0005108	Abnormality of the intervertebral disk
HP:0005109	Abnormality of the Achilles tendon
HP:0005110	Atrial fibrillation
HP:0005111	obsolete Dilatation of the ascending aorta
HP:0005112	Abdominal aortic aneurysm
HP:0005113	Aortic arch aneurysm
HP:0005114	obsolete Abnormalities of the peripheral arteries
HP:0005115	Supraventricular arrhythmia
HP:0005116	Arterial tortuosity
HP:0005117	Elevated diastolic blood pressure
HP:0005120	Abnormal cardiac atrium morphology
HP:0005121	Posterior scalloping of vertebral bodies
HP:0005129	Congenital hypertrophy of left ventricle
HP:0005130	Restrictive heart failure
HP:0005132	Pericardial constriction
HP:0005133	Right ventricular dilatation
HP:0005134	Absence of the pulmonary valve
HP:0005135	Abnormal T-wave
HP:0005136	Mitral annular calcification
HP:0005141	obsolete Episodes of ventricular tachycardia
HP:0005143	Anomalous origin of right pulmonary artery from ascending aorta
HP:0005144	Ventricular septal hypertrophy
HP:0005145	Coronary artery stenosis
HP:0005146	Cardiac valve calcification
HP:0005147	Bidirectional ventricular ectopy
HP:0005148	Pulmonary valve defects
HP:0005150	Abnormal atrioventricular conduction
HP:0005151	Preductal coarctation of the aorta
HP:0005152	Histiocytoid cardiomyopathy
HP:0005155	Ventricular escape rhythm
HP:0005156	Hypoplastic left atrium
HP:0005157	Concentric hypertrophic cardiomyopathy
HP:0005160	Total anomalous pulmonary venous return
HP:0005162	Left ventricular dysfunction
HP:0005164	Dysplastic pulmonary valve
HP:0005165	Shortened PR interval
HP:0005168	Elevated right atrial pressure
HP:0005170	Complete heart block with broad QRS complexes
HP:0005172	Left posterior fascicular block
HP:0005173	obsolete Calcific aortic valve stenosis
HP:0005174	Membranous subvalvular aortic stenosis
HP:0005176	Dysplastic aortic valve
HP:0005177	Premature arteriosclerosis
HP:0005178	Complete heart block with narrow QRS complexes
HP:0005180	Tricuspid regurgitation
HP:0005181	Premature coronary artery atherosclerosis
HP:0005182	Bicuspid pulmonary valve
HP:0005183	Pericardial lymphangiectasia
HP:0005184	Prolonged QTc interval
HP:0005185	Global systolic dysfunction
HP:0005186	Synovial hypertrophy
HP:0005187	Progressive joint destruction
HP:0005190	Proximal finger joint hyperextensibility
HP:0005191	Congenital knee dislocation
HP:0005193	Restricted large joint movement
HP:0005194	Flattened metatarsal heads
HP:0005195	Polyarticular arthropathy
HP:0005197	Generalized morning stiffness
HP:0005198	Stiff interphalangeal joints
HP:0005199	Aplasia of the abdominal wall musculature
HP:0005200	Retroperitoneal fibrosis
HP:0005201	Anomalous splenoportal venous system
HP:0005202	Helicobacter pylori infection
HP:0005203	Spontaneous esophageal perforation
HP:0005206	Pancreatic pseudocyst
HP:0005207	Gastric hypertrophy
HP:0005208	Secretory diarrhea
HP:0005209	Intrahepatic bile duct cysts
HP:0005210	Hypoplastic colon
HP:0005211	Midgut malrotation
HP:0005212	Anal mucosal leukoplakia
HP:0005213	Pancreatic calcification
HP:0005214	Intestinal obstruction
HP:0005215	Frequent Giardia lamblia infestation
HP:0005216	Impaired mastication
HP:0005217	Duplication of internal organs
HP:0005218	Anoperineal fistula
HP:0005219	Absence of intrinsic factor
HP:0005220	Multiple intestinal neurofibromatosis
HP:0005222	Bowel diverticulosis
HP:0005223	Duplicated colon
HP:0005224	Rectal abscess
HP:0005225	Intestinal edema
HP:0005227	Adenomatous colonic polyposis
HP:0005229	Jejunoileal ulceration
HP:0005230	Biliary tract obstruction
HP:0005231	Chronic gastritis
HP:0005232	Pancreatic dysplasia
HP:0005233	Hypoplasia of the gallbladder
HP:0005234	Neonatal intestinal obstruction
HP:0005235	Jejunal atresia
HP:0005236	Chronic calcifying pancreatitis
HP:0005237	Degenerative liver disease
HP:0005238	Discrete intestinal polyps
HP:0005240	Esophageal obstruction
HP:0005241	Total intestinal aganglionosis
HP:0005242	Extrahepatic biliary duct atresia
HP:0005243	Partial abdominal muscle agenesis
HP:0005244	Gastrointestinal infarctions
HP:0005245	Intestinal hypoplasia
HP:0005246	Giant hypertrophic gastritis
HP:0005247	Hypoplasia of the abdominal wall musculature
HP:0005248	Intrahepatic biliary atresia
HP:0005249	Functional intestinal obstruction
HP:0005250	High intestinal obstruction
HP:0005253	Increased anterioposterior diameter of thorax
HP:0005254	Unilateral chest hypoplasia
HP:0005255	Absence of pectoralis minor muscle
HP:0005256	Unilateral absence of pectoralis major muscle
HP:0005257	Thoracic hypoplasia
HP:0005258	Pectoral muscle hypoplasia/aplasia
HP:0005259	Abnormal facility in opposing the shoulders
HP:0005261	Joint hemorrhage
HP:0005262	Abnormality of the synovia
HP:0005263	Gastritis
HP:0005264	Abnormality of the gallbladder
HP:0005265	Abnormality of the jejunum
HP:0005266	Intestinal polyp
HP:0005267	Premature delivery because of cervical insufficiency or membrane fragility
HP:0005268	Spontaneous abortion
HP:0005272	Prominent nasolabial fold
HP:0005273	Absent nasal septal cartilage
HP:0005274	Prominent nasal tip
HP:0005275	Cartilaginous ossification of nose
HP:0005278	Hypoplastic nasal tip
HP:0005280	Depressed nasal bridge
HP:0005281	Hypoplastic nasal bridge
HP:0005285	Absent nasal bridge
HP:0005288	Abnormality of the nares
HP:0005289	Abnormality of the nasolabial region
HP:0005290	Internal carotid artery hypoplasia
HP:0005291	Inflammatory arteriopathy
HP:0005292	Intimal thickening in the coronary arteries
HP:0005293	Venous insufficiency
HP:0005294	Arterial dissection
HP:0005295	Pseudocoarctation of the aorta
HP:0005296	obsolete Occlusive vascular disease
HP:0005297	Premature occlusive vascular stenosis
HP:0005298	obsolete Atrioventricular canal defect with right ventricle aorta and pulmonary atresia
HP:0005299	obsolete Premature peripheral vascular disease
HP:0005300	Nodular inflammatory vasculitis
HP:0005301	Persistent left superior vena cava
HP:0005302	Carotid artery tortuosity
HP:0005303	Aortic arch calcification
HP:0005304	Hypoplastic pulmonary veins
HP:0005305	Cerebral venous thrombosis
HP:0005306	Capillary hemangioma
HP:0005307	Postural hypotension with compensatory tachycardia
HP:0005308	Pulmonary artery vasoconstriction
HP:0005309	obsolete Peripheral vascular insufficiency
HP:0005310	Large vessel vasculitis
HP:0005311	Agenesis of pulmonary vessels
HP:0005312	Pulmonary aterial intimal fibrosis
HP:0005313	Arterial fibromuscular dysplasia
HP:0005314	Anomalous branches of internal carotid artery
HP:0005315	obsolete Peripheral artery occlusive disease
HP:0005316	Peripheral pulmonary vessel aplasia
HP:0005317	Increased pulmonary vascular resistance
HP:0005318	Cerebral vasculitis
HP:0005320	Lack of facial subcutaneous fat
HP:0005321	Mandibulofacial dysostosis
HP:0005322	Prominent nasal septum
HP:0005323	Hemifacial hypertrophy
HP:0005324	Disturbance of facial expression
HP:0005325	Extension of hair growth on temples to lateral eyebrow
HP:0005326	Hypoplastic philtrum
HP:0005327	Loss of facial expression
HP:0005328	Progeroid facial appearance
HP:0005329	Fixed facial expression
HP:0005332	Recurrent mandibular subluxations
HP:0005335	Sleepy facial expression
HP:0005336	Forehead hyperpigmentation
HP:0005338	Sparse lateral eyebrow
HP:0005339	Abnormality of complement system
HP:0005340	Spastic/hyperactive bladder
HP:0005341	Autonomic bladder dysfunction
HP:0005343	Hypoplasia of the bladder
HP:0005344	Abnormal carotid artery morphology
HP:0005345	Abnormal vena cava morphology
HP:0005346	Abnormal facial expression
HP:0005347	Cartilaginous trachea
HP:0005348	Inspiratory stridor
HP:0005349	Hypoplasia of the epiglottis
HP:0005352	Severe T-cell immunodeficiency
HP:0005353	Recurrent herpes
HP:0005354	Lack of T cell function
HP:0005356	Decreased serum complement factor I
HP:0005357	Defective B cell differentiation
HP:0005359	Aplasia of the thymus
HP:0005360	Susceptibility to chickenpox
HP:0005363	Humoral immunodeficiency
HP:0005364	Severe viral infections
HP:0005365	Severe B lymphocytopenia
HP:0005366	Recurrent streptococcus pneumoniae infections
HP:0005368	Abnormality of humoral immunity
HP:0005369	Decreased serum complement factor H
HP:0005372	Abnormality of B cell physiology
HP:0005374	Cellular immunodeficiency
HP:0005375	obsolete Partial cellular immunodeficiency
HP:0005376	Recurrent Haemophilus influenzae infections
HP:0005379	obsolete Severe T lymphocytopenia
HP:0005381	Recurrent meningococcal disease
HP:0005384	Defective B cell activation
HP:0005386	Recurrent protozoan infections
HP:0005387	Combined immunodeficiency
HP:0005389	Depletion of components of the alternative complement pathway
HP:0005390	Recurrent opportunistic infections
HP:0005396	Susceptibility to coronavirus 229e
HP:0005397	obsolete Exaggerated cellular immune processes
HP:0005400	Reduction of neutrophil motility
HP:0005401	Recurrent candida infections
HP:0005402	obsolete Primary T-lymphocyte immune abnormalities
HP:0005403	Decrease in T cell count
HP:0005404	Increased B cell count
HP:0005406	Recurrent bacterial skin infections
HP:0005407	Decreased proportion of CD4-positive T cells
HP:0005409	obsolete Markedly reduced T cell function
HP:0005411	Chronic intestinal candidiasis
HP:0005413	Increased alpha-globulin
HP:0005415	Decreased proportion of CD8-positive T cells
HP:0005416	Decreased serum complement factor B
HP:0005419	Decreased T cell activation
HP:0005420	Recurrent gram-negative bacterial infections
HP:0005421	Decreased serum complement C3
HP:0005422	Absence of CD8-positive T cells
HP:0005423	Dysfunctional alternative complement pathway
HP:0005424	Absent specific antibody response
HP:0005425	Recurrent sinopulmonary infections
HP:0005428	Severe recurrent varicella
HP:0005429	Recurrent systemic pyogenic infections
HP:0005430	Recurrent Neisserial infections
HP:0005432	Transient hypogammaglobulinemia of infancy
HP:0005435	Impaired T cell function
HP:0005437	Recurrent infections in infancy and early childhood
HP:0005439	Maxillozygomatic hypoplasia
HP:0005441	Sclerotic cranial sutures
HP:0005442	Widely patent coronal suture
HP:0005445	Widened posterior fossa
HP:0005446	Obtuse angle of mandible
HP:0005449	Bridged sella turcica
HP:0005450	Calvarial osteosclerosis
HP:0005451	Decreased cranial base ossification
HP:0005453	Absent/hypoplastic paranasal sinuses
HP:0005456	Absent ethmoidal sinuses
HP:0005458	Premature closure of fontanelles
HP:0005461	Craniofacial disproportion
HP:0005462	Calcification of falx cerebri
HP:0005463	Elongated sella turcica
HP:0005464	Craniofacial osteosclerosis
HP:0005465	Facial hyperostosis
HP:0005466	Hypoplasia of the frontal bone
HP:0005469	Flat occiput
HP:0005472	Orbital craniosynostosis
HP:0005473	Fusion of middle ear ossicles
HP:0005474	Decreased calvarial ossification
HP:0005476	Widely patent sagittal suture
HP:0005477	Progressive sclerosis of skull base
HP:0005478	Prominent frontal sinuses
HP:0005479	Decreased circulating total IgE
HP:0005482	Abnormality of the alternative complement pathway
HP:0005483	Abnormal epiglottis morphology
HP:0005484	Postnatal microcephaly
HP:0005486	Small fontanelle
HP:0005487	Prominent metopic ridge
HP:0005490	Postnatal macrocephaly
HP:0005494	Premature posterior fontanelle closure
HP:0005495	Metopic suture patent to nasal root
HP:0005498	Midline skin dimples over anterior/posterior fontanelles
HP:0005502	Increased red cell osmotic fragility
HP:0005505	Refractory anemia
HP:0005506	Chronic myelogenous leukemia
HP:0005507	Hemoglobin Barts
HP:0005508	Monoclonal immunoglobulin M proteinemia
HP:0005510	Transient erythroblastopenia
HP:0005511	Heinz body anemia
HP:0005512	Impaired neutrophil killing of staphylococci
HP:0005513	Increased megakaryocyte count
HP:0005517	T-cell lymphoma/leukemia
HP:0005518	Increased mean corpuscular volume
HP:0005520	Chronic disseminated intravascular coagulation
HP:0005521	Disseminated intravascular coagulation
HP:0005522	Pyridoxine-responsive sideroblastic anemia
HP:0005523	Lymphoproliferative disorder
HP:0005524	Macrocytic hemolytic disease
HP:0005525	Spontaneous hemolytic crises
HP:0005526	Lymphoid leukemia
HP:0005527	Reduced kininogen activity
HP:0005528	Bone marrow hypocellularity
HP:0005531	Biphenotypic acute leukaemia
HP:0005532	Macrocytic dyserythropoietic anemia
HP:0005534	Transient myeloproliferative syndrome
HP:0005535	Exercise-induced hemolysis
HP:0005537	Decreased mean platelet volume
HP:0005539	T cell chronic lymphocytic lymphoma/leukemia
HP:0005540	Red blood cell keratocytosis
HP:0005541	Congenital agranulocytosis
HP:0005542	Prolonged whole-blood clotting time
HP:0005543	Reduced protein C activity
HP:0005546	Increased red cell osmotic resistance
HP:0005547	Myeloproliferative disorder
HP:0005548	Megakaryocytopenia
HP:0005549	obsolete Congenital neutropenia
HP:0005550	Chronic lymphatic leukemia
HP:0005556	Abnormality of the metopic suture
HP:0005557	Abnormality of the zygomatic arch
HP:0005558	Chronic leukemia
HP:0005559	Abnormality of the kinin-kallikrein system
HP:0005560	Imbalanced hemoglobin synthesis
HP:0005561	Abnormality of bone marrow cell morphology
HP:0005562	Multiple renal cysts
HP:0005563	Decreased numbers of nephrons
HP:0005564	Absence of renal corticomedullary differentiation
HP:0005565	Reduced renal corticomedullary differentiation
HP:0005567	Renal magnesium wasting
HP:0005571	Increased renal tubular phosphate reabsorption
HP:0005572	Decreased renal tubular phosphate excretion
HP:0005574	Non-acidotic proximal tubulopathy
HP:0005575	Hemolytic-uremic syndrome
HP:0005576	Tubulointerstitial fibrosis
HP:0005579	Impaired reabsorption of chloride
HP:0005580	Duplication of renal pelvis
HP:0005583	Tubular basement membrane disintegration
HP:0005584	Renal cell carcinoma
HP:0005585	Spotty hyperpigmentation
HP:0005586	Hyperpigmentation in sun-exposed areas
HP:0005587	Profuse pigmented skin lesions
HP:0005588	Patchy palmoplantar keratoderma
HP:0005590	Spotty hypopigmentation
HP:0005592	Giant melanosomes in melanocytes
HP:0005593	Macular hypopigmented whorls, streaks, and patches
HP:0005595	Generalized hyperkeratosis
HP:0005597	Congenital alopecia totalis
HP:0005598	Facial telangiectasia in butterfly midface distribution
HP:0005599	Hypopigmentation of hair
HP:0005600	Congenital giant melanocytic nevus
HP:0005602	Progressive vitiligo
HP:0005603	Numerous congenital melanocytic nevi
HP:0005605	Large cafe-au-lait macules with irregular margins
HP:0005606	Hyperpigmented nevi and streak
HP:0005607	Abnormal tracheobronchial morphology
HP:0005608	Bilobate gallbladder
HP:0005609	Gallbladder dysfunction
HP:0005612	Arthrogryposis-like hand anomaly
HP:0005613	Aplasia/hypoplasia of the femur
HP:0005616	Accelerated skeletal maturation
HP:0005617	Bilateral camptodactyly
HP:0005619	Thoracolumbar kyphosis
HP:0005620	Hypermobility of interphalangeal joints
HP:0005621	Trapezoidal shaped vertebral bodies
HP:0005622	Broad long bones
HP:0005623	Absent ossification of calvaria
HP:0005625	Osteoporosis of vertebrae
HP:0005626	Posterior fusion of lumbosacral vertebrae
HP:0005627	Type D brachydactyly
HP:0005632	Absent forearm
HP:0005638	Decreased anterioposterior diameter of lumbar vertebral bodies
HP:0005639	Hyperextensible hand joints
HP:0005640	Abnormal vertebral segmentation and fusion
HP:0005643	Short 3rd toe
HP:0005645	Intervertebral disk calcification
HP:0005648	Bilateral ulnar hypoplasia
HP:0005650	Cutaneous syndactyly between fingers 2 and 5
HP:0005652	Cortical sclerosis
HP:0005653	Moderate generalized osteoporosis
HP:0005655	Multiple digital exostoses
HP:0005656	Positional foot deformity
HP:0005659	Thoracic kyphoscoliosis
HP:0005661	Salmonella osteomyelitis
HP:0005665	Massively thickened long bone cortices
HP:0005667	Os odontoideum
HP:0005671	Bilateral intracranial calcifications
HP:0005676	Rudimentary postaxial polydactyly of hands
HP:0005678	Anterior atlanto-occipital dislocation
HP:0005679	Dupuytren contracture
HP:0005680	Tongue-like lumbar vertebral deformities
HP:0005681	Juvenile rheumatoid arthritis
HP:0005682	Talocalcaneal synostosis
HP:0005684	Distal arthrogryposis
HP:0005686	Patchy osteosclerosis
HP:0005687	Deformed humeral heads
HP:0005688	Dysplastic distal thumb phalanges with a central hole
HP:0005689	Dermatoglyphic ridges abnormal
HP:0005692	Joint hyperflexibility
HP:0005694	Partial fusion of proximal row of carpal bones
HP:0005696	Postaxial polydactyly type A
HP:0005700	Increased bone density with cystic changes
HP:0005701	Multiple enchondromatosis
HP:0005707	Bilateral triphalangeal thumbs
HP:0005709	2-3 toe cutaneous syndactyly
HP:0005715	Flattened knee epiphyses
HP:0005716	Lethal skeletal dysplasia
HP:0005720	Shortening of all metacarpals
HP:0005722	Hyperextensible thumb
HP:0005723	Shoe-shaped sella turcica
HP:0005725	Nonopposable triphalangeal thumb
HP:0005726	Thumbs hypoplastic with bulbous tips
HP:0005731	Cortical irregularity
HP:0005733	Spinal stenosis with reduced interpedicular distance
HP:0005736	Short tibia
HP:0005739	Posterior subluxation of radial head
HP:0005743	Avascular necrosis of the capital femoral epiphysis
HP:0005744	obsolete Generalized osteoporosis with pathologic fractures
HP:0005745	Congenital foot contractures
HP:0005746	Osteosclerosis of the base of the skull
HP:0005747	Easily subluxated first metacarpophalangeal joints
HP:0005750	Contractures of the joints of the lower limbs
HP:0005752	Flattened moderately deformed vertebrae
HP:0005756	Neonatal epiphyseal stippling
HP:0005758	Basilar impression
HP:0005759	Small flat posterior fossa
HP:0005764	Polyarticular arthritis
HP:0005765	Sacral meningocele
HP:0005766	Disproportionate shortening of the tibia
HP:0005767	1-2 toe complete cutaneous syndactyly
HP:0005768	2-4 toe cutaneous syndactyly
HP:0005769	Fifth finger distal phalanx clinodactyly
HP:0005772	Aplasia/Hypoplasia of the tibia
HP:0005773	Short forearm
HP:0005775	Multiple skeletal anomalies
HP:0005776	Carpal bone malsegmentation
HP:0005780	Absent fourth finger distal interphalangeal crease
HP:0005781	Contractures of the large joints
HP:0005787	Lumbar platyspondyly
HP:0005788	Abnormal cervical myelogram
HP:0005789	Generalized osteosclerosis
HP:0005790	Short mandibular condyles
HP:0005791	Cortical thickening of long bone diaphyses
HP:0005792	Short humerus
HP:0005793	Shortening of all distal phalanges of the toes
HP:0005794	obsolete Arterial disease of legs
HP:0005798	Posterior radial head dislocation
HP:0005802	Coalescence of tarsal bones
HP:0005807	Absent distal phalanges
HP:0005815	Supernumerary ribs
HP:0005817	Postaxial polysyndactyly of foot
HP:0005819	Short middle phalanx of finger
HP:0005820	Superior rib anomalies
HP:0005824	Clinodactyly of the 2nd toe
HP:0005825	Mixed sclerosis of humeral metaphyses
HP:0005828	Transient pulmonary infiltrates
HP:0005829	Maldevelopment of radioulnar joint
HP:0005830	Flexion contracture of toe
HP:0005831	Type B brachydactyly
HP:0005832	Dysharmonic delayed bone age
HP:0005833	obsolete Joint swelling onset late infancy
HP:0005834	obsolete Thumbs hypo/aplastic
HP:0005837	obsolete Joint dislocations in young adult
HP:0005841	Calcific stippling of infantile cartilaginous skeleton
HP:0005844	Rounded middle phalanx of finger
HP:0005848	Bifid thumb distal phalanx
HP:0005849	Diffuse cerebral calcification
HP:0005850	Congenital talipes calcaneovalgus
HP:0005852	Limited elbow extension and supination
HP:0005853	Congenital foot contraction deformities
HP:0005855	Multiple prenatal fractures
HP:0005856	Ulnar radial head dislocation
HP:0005857	Cervical spina bifida
HP:0005863	Type E brachydactyly
HP:0005864	Pseudoarthrosis
HP:0005866	Opposable triphalangeal thumb
HP:0005867	Fused fourth and fifth metacarpals
HP:0005868	Metaphyseal enchondromatosis
HP:0005871	Metaphyseal chondrodysplasia
HP:0005872	Brachytelomesophalangy
HP:0005873	Polysyndactyly of hallux
HP:0005875	Increased dermatoglyphic whorls
HP:0005876	Progressive flexion contractures
HP:0005877	Multiple small vertebral fractures
HP:0005878	Enlarged sagittal diameter of the cervical canal
HP:0005879	Congenital finger flexion contractures
HP:0005880	Metacarpophalangeal synostosis
HP:0005881	Spinal instability
HP:0005882	Dermatoglyphic variants
HP:0005885	Absent ossification of cervical vertebral bodies
HP:0005886	Aphalangy of the hands
HP:0005890	Hyperostosis cranialis interna
HP:0005891	Progressive forearm bowing
HP:0005892	Proximal tibial and fibular fusion
HP:0005894	Double first metacarpals
HP:0005895	Radial deviation of thumb terminal phalanx
HP:0005897	Severe generalized osteoporosis
HP:0005899	Metaphyseal dysostosis
HP:0005900	Fifth metacarpal with ulnar notch
HP:0005901	Chronic recurrent multifocal osteomyelitis
HP:0005905	Abnormal cervical curvature
HP:0005906	Delayed pneumatization of the mastoid process
HP:0005910	Rhomboid or triangular shaped 5th finger middle phalanx
HP:0005912	Biliary atresia
HP:0005913	Abnormality of metacarpal epiphyses
HP:0005914	Aplasia/Hypoplasia involving the metacarpal bones
HP:0005916	Abnormal metacarpal morphology
HP:0005917	Supernumerary metacarpal bones
HP:0005918	Abnormal finger phalanx morphology
HP:0005920	Abnormal epiphysis morphology of the phalanges of the hand
HP:0005921	obsolete Abnormal ossification of hand bones
HP:0005922	Abnormal hand morphology
HP:0005923	Abnormalities of the metaphyses of the hand
HP:0005924	Abnormality of the epiphyses of the hand
HP:0005925	Abnormalities of the diaphyses of the hand
HP:0005926	Abnormality of hand cortical bone
HP:0005927	Aplasia/hypoplasia involving bones of the hand
HP:0005928	Synostosis involving the fibula
HP:0005929	Synostosis involving the tibia
HP:0005930	Abnormality of epiphysis morphology
HP:0005932	Abnormal renal corticomedullary differentiation
HP:0005934	Imperfect vocal cord adduction
HP:0005938	Abnormal respiratory motile cilium morphology
HP:0005939	Multiple bilateral pneumothoraces
HP:0005941	Intermittent hyperpnea at rest
HP:0005942	Desquamative interstitial pneumonitis
HP:0005943	Respiratory arrest
HP:0005944	Bilateral lung agenesis
HP:0005945	Laryngeal obstruction
HP:0005946	Ventilator dependence with inability to wean
HP:0005947	Decreased sensitivity to hypoxemia
HP:0005948	Cystic lung disease
HP:0005949	Apneic episodes in infancy
HP:0005950	Laryngeal web
HP:0005951	Progressive inspiratory stridor
HP:0005952	Decreased pulmonary function
HP:0005954	Pulmonary capillary hemangiomatosis
HP:0005956	Anteroposteriorly shortened larynx
HP:0005957	Breathing dysregulation
HP:0005959	Impaired gluconeogenesis
HP:0005961	Hypoargininemia
HP:0005964	Intermittent hypothermia
HP:0005967	Mixed respiratory and metabolic acidosis
HP:0005968	Temperature instability
HP:0005972	Respiratory acidosis
HP:0005973	Fructose intolerance
HP:0005974	Episodic ketoacidosis
HP:0005976	Hyperkalemic metabolic acidosis
HP:0005977	Hypochloremic metabolic alkalosis
HP:0005978	Type II diabetes mellitus
HP:0005979	Metabolic ketoacidosis
HP:0005982	Reduced phenylalanine hydroxylase activity
HP:0005984	Elevated maternal serum alpha-fetoprotein
HP:0005986	Limitation of neck motion
HP:0005987	Multinodular goiter
HP:0005988	Congenital muscular torticollis
HP:0005989	Redundant neck skin
HP:0005990	Thyroid hypoplasia
HP:0005991	Limited neck flexion
HP:0005994	Nodular goiter
HP:0005995	Decreased adipose tissue around neck
HP:0005997	Restricted neck movement due to contractures
HP:0005999	Ureteral atresia
HP:0006000	Ureteral obstruction
HP:0006006	Hypotrophy of the small hand muscles
HP:0006008	Unilateral brachydactyly
HP:0006009	Broad phalanx
HP:0006011	Cuboidal metacarpal
HP:0006012	Widened metacarpal shaft
HP:0006014	Abnormally shaped carpal bones
HP:0006016	Delayed phalangeal epiphyseal ossification
HP:0006019	Reduced proximal interphalangeal joint space
HP:0006026	Rounded epiphyses
HP:0006028	Metaphyseal cupping of metacarpals
HP:0006035	Cone-shaped epiphyses of phalanges 2 to 5
HP:0006040	Long second metacarpal
HP:0006042	Y-shaped metacarpals
HP:0006045	Short pointed phalanges
HP:0006048	Distal widening of metacarpals
HP:0006051	Metacarpal periosteal thickening
HP:0006055	Ulnar deviated club hands
HP:0006059	Cone-shaped metacarpal epiphyses
HP:0006060	Tombstone-shaped proximal phalanges
HP:0006064	Limited interphalangeal movement
HP:0006067	Multiple carpal ossification centers
HP:0006069	Severe carpal ossification delay
HP:0006070	Metacarpophalangeal joint contracture
HP:0006077	Absent proximal finger flexion creases
HP:0006086	Thin metacarpal cortices
HP:0006088	1-5 finger complete cutaneous syndactyly
HP:0006089	Palmar hyperhidrosis
HP:0006092	Malaligned carpal bone
HP:0006094	Finger joint hypermobility
HP:0006095	Wide tufts of distal phalanges
HP:0006097	3-4 finger syndactyly
HP:0006099	Metacarpophalangeal joint hyperextensibility
HP:0006101	Finger syndactyly
HP:0006106	Absent trapezoid bone
HP:0006107	Fingerpad telangiectases
HP:0006108	Tapered metacarpals
HP:0006109	Absent phalangeal crease
HP:0006110	Shortening of all middle phalanges of the fingers
HP:0006112	Expanded phalanges with widened medullary cavities
HP:0006114	Multiple palmar creases
HP:0006118	Shortening of all distal phalanges of the fingers
HP:0006119	Proximal tapering of metacarpals
HP:0006121	Acral ulceration
HP:0006127	Long proximal phalanx of finger
HP:0006129	Drumstick terminal phalanges
HP:0006134	Enlarged metacarpal epiphyses
HP:0006135	Decreased finger mobility
HP:0006136	Bilateral postaxial polydactyly
HP:0006140	Premature fusion of phalangeal epiphyses
HP:0006143	Abnormal finger flexion creases
HP:0006144	Shortening of all proximal phalanges of the fingers
HP:0006145	Central Y-shaped metacarpal
HP:0006146	Broad metacarpal epiphyses
HP:0006147	Progressive fusion 2nd-5th pip joints
HP:0006149	Increased laxity of fingers
HP:0006150	Swan neck-like deformities of the fingers
HP:0006152	Proximal symphalangism of hands
HP:0006153	Disharmonious carpal bone
HP:0006155	Long phalanx of finger
HP:0006156	Ulnar deviation of thumb
HP:0006157	Prominent palmar flexion creases
HP:0006158	obsolete Finger joint hyperextensibility
HP:0006159	Mesoaxial hand polydactyly
HP:0006160	Irregular metacarpals
HP:0006161	Short metacarpals with rounded proximal ends
HP:0006162	Soft tissue swelling of interphalangeal joints
HP:0006163	Enlarged metacarpophalangeal joints
HP:0006165	Proportionate shortening of all digits
HP:0006166	Tubular metacarpal bones
HP:0006167	Prominent proximal interphalangeal joints
HP:0006169	Decreased mobility 3rd-5th fingers
HP:0006170	Chess-pawn distal phalanges
HP:0006172	Flattened, squared-off epiphyses of tubular bones
HP:0006174	Metacarpal diaphyseal endosteal sclerosis
HP:0006175	Proximal phalangeal periosteal thickening
HP:0006176	Two carpal ossification centers present at birth
HP:0006179	Pseudoepiphyses of second metacarpal
HP:0006180	Crowded carpal bones
HP:0006184	Decreased palmar creases
HP:0006185	Enlarged proximal interphalangeal joints
HP:0006187	Fusion of midphalangeal joints
HP:0006189	Prominent interdigital folds
HP:0006190	Radially deviated wrists
HP:0006191	Deep palmar crease
HP:0006192	Tapered phalanx of finger
HP:0006193	Thimble-shaped middle phalanges of hand
HP:0006200	Widened distal phalanges
HP:0006201	Hypermobility of distal interphalangeal joints
HP:0006202	Osteolysis of scaphoids
HP:0006203	Decreased movement range in interphalangeal joints
HP:0006205	Irregular phalanges
HP:0006206	Hypersegmentation of proximal phalanx of second finger
HP:0006207	Partial fusion of carpals
HP:0006208	Metaphyseal cupping of proximal phalanges
HP:0006209	Partial-complete absence of 5th phalanges
HP:0006210	Postaxial oligodactyly
HP:0006213	Thin proximal phalanges with broad epiphyses of the hand
HP:0006216	Single interphalangeal crease of fifth finger
HP:0006217	Limited mobility of proximal interphalangeal joint
HP:0006224	Tapering pointed ends of distal finger phalanges
HP:0006226	Osteoarthritis of the first carpometacarpal joint
HP:0006228	Valgus hand deformity
HP:0006230	Unilateral oligodactyly
HP:0006232	Expanded metacarpals with widened medullary cavities
HP:0006233	Osteoarthritis of the distal interphalangeal joint
HP:0006234	Osteolysis involving tarsal bones
HP:0006236	Slender metacarpals
HP:0006237	Prominent interphalangeal joints
HP:0006239	Shortening of all middle phalanges of the toes
HP:0006243	Phalangeal dislocation
HP:0006247	Enlarged interphalangeal joints
HP:0006248	Limited wrist movement
HP:0006251	Limited wrist extension
HP:0006252	Interphalangeal joint erosions
HP:0006253	Swelling of proximal interphalangeal joints
HP:0006254	Elevated alpha-fetoprotein
HP:0006256	Abnormality of hand joint mobility
HP:0006257	Abnormality of carpal bone ossification
HP:0006261	Abnormal phalangeal joint morphology of the hand
HP:0006262	Aplasia/Hypoplasia of the 5th finger
HP:0006263	Abnormality of the epiphyses of the 2nd finger
HP:0006264	Aplasia/Hypoplasia of the 2nd finger
HP:0006265	Aplasia/Hypoplasia of fingers
HP:0006266	Small placenta
HP:0006267	Large placenta
HP:0006268	Fluctuating splenomegaly
HP:0006270	Hypoplastic spleen
HP:0006273	Pancreatic lymphangiectasis
HP:0006274	Reduced pancreatic beta cells
HP:0006276	Hyperechogenic pancreas
HP:0006277	Pancreatic hyperplasia
HP:0006278	Ectopic pancreatic tissue
HP:0006279	Beta-cell dysfunction
HP:0006280	Chronic pancreatitis
HP:0006282	Generalized hypoplasia of dental enamel
HP:0006283	Multiple unerupted teeth
HP:0006285	Hypomineralization of enamel
HP:0006286	Yellow-brown discoloration of the teeth
HP:0006288	Advanced eruption of teeth
HP:0006289	Agenesis of central incisor
HP:0006290	Discolored lateral incisors
HP:0006291	Marked delay in eruption of permanent teeth
HP:0006292	Abnormality of dental eruption
HP:0006293	Agenesis of maxillary central incisor
HP:0006297	Hypoplasia of dental enamel
HP:0006298	Prolonged bleeding after dental extraction
HP:0006302	Dagger-shaped pulp calcifications
HP:0006304	Widely-spaced incisors
HP:0006308	Atrophy of alveolar ridges
HP:0006311	Generalized microdontia
HP:0006313	Widely spaced primary teeth
HP:0006315	Single median maxillary incisor
HP:0006316	Irregularly spaced teeth
HP:0006321	Multiple non-erupting secondary teeth
HP:0006323	Premature loss of primary teeth
HP:0006326	Buried teeth encased in mucopolysaccharide
HP:0006329	Alveolar process hypoplasia
HP:0006330	Rotated maxillary central incisors
HP:0006332	Supernumerary maxillary incisor
HP:0006333	Crowded maxillary incisors
HP:0006334	Hypoplasia of the primary teeth
HP:0006335	Persistence of primary teeth
HP:0006336	Short dental roots
HP:0006337	Premature eruption of permanent teeth
HP:0006338	Malformation of mandibular premolar
HP:0006339	Conical mandibular incisor
HP:0006342	Peg-shaped maxillary lateral incisors
HP:0006344	Abnormality of primary molar morphology
HP:0006346	Screwdriver-shaped incisors
HP:0006347	Microdontia of primary teeth
HP:0006349	Agenesis of permanent teeth
HP:0006350	Obliteration of the pulp chamber
HP:0006352	Failure of eruption of permanent teeth
HP:0006353	Hypoplasia of the tooth germ
HP:0006355	Agenesis of mandibular central incisor
HP:0006357	Premature loss of permanent teeth
HP:0006358	Shovel-shaped maxillary central incisors
HP:0006361	Irregular femoral epiphysis
HP:0006362	Varus deformity of humeral neck
HP:0006366	Adductor longus contractures
HP:0006367	Crumpled long bones
HP:0006368	Forearm reduction defects
HP:0006369	Irregular patellae
HP:0006370	Distal ulnar epiphyseal stippling
HP:0006371	Broad long bone diaphyses
HP:0006375	Dumbbell-shaped femur
HP:0006376	Limited elbow flexion
HP:0006378	Osteolysis of patellae
HP:0006379	Proximal tibial hypoplasia
HP:0006380	Knee flexion contracture
HP:0006381	Rudimentary fibula
HP:0006383	Progressive bowing of long bones
HP:0006384	Club-shaped distal femur
HP:0006385	Short lower limbs
HP:0006386	Hypoplastic distal radial epiphyses
HP:0006387	Wide distal femoral metaphysis
HP:0006389	Limited knee flexion
HP:0006390	Anterior tibial bowing
HP:0006391	Overtubulated long bones
HP:0006392	Increased density of long bones
HP:0006394	Limited pronation/supination of forearm
HP:0006397	Lateral displacement of patellae
HP:0006398	Flat distal femoral epiphysis
HP:0006400	Absent knee epiphyses
HP:0006402	Distal shortening of limbs
HP:0006406	Club-shaped proximal femur
HP:0006407	Irregular distal femoral epiphysis
HP:0006408	Distal tapering femur
HP:0006409	Progressive leg bowing
HP:0006413	Broad tibial metaphyses
HP:0006414	Distal tibial bowing
HP:0006415	Cortically dense long tubular bones
HP:0006417	Broad femoral metaphyses
HP:0006420	Asymmetric radial dysplasia
HP:0006423	Peg-like central prominence of distal tibial metaphyses
HP:0006424	Elongated radius
HP:0006426	Rudimentary to absent tibiae
HP:0006429	Broad femoral neck
HP:0006431	Proximal femoral metaphyseal abnormality
HP:0006432	Trapezoidal distal femoral condyles
HP:0006433	Dysplastic radii
HP:0006434	Hypoplasia of proximal radius
HP:0006436	Shortening of the tibia
HP:0006437	Disproportionate prominence of the femoral medial condyle
HP:0006438	Enlargement of the distal femoral epiphysis
HP:0006439	Radioulnar dislocation
HP:0006440	Increased density of long bone diaphyses
HP:0006441	Lateral humeral condyle aplasia
HP:0006442	Hypoplasia of proximal fibula
HP:0006443	Patellar aplasia
HP:0006446	Dysplastic patella
HP:0006449	Distal radial epiphyseal osteolysis
HP:0006450	Multicentric ossification of proximal femoral epiphyses
HP:0006453	Lateral displacement of the femoral head
HP:0006454	Delayed patellar ossification
HP:0006456	Irregular proximal tibial epiphyses
HP:0006459	Dorsal subluxation of ulna
HP:0006460	Increased laxity of ankles
HP:0006461	Proximal femoral epiphysiolysis
HP:0006462	Generalized bone demineralization
HP:0006463	Rickets of the lower limbs
HP:0006465	Periosteal thickening of long tubular bones
HP:0006466	Ankle contracture
HP:0006467	Limited shoulder movement
HP:0006470	Thin long bone diaphyses
HP:0006471	Fixed elbow flexion
HP:0006473	Anterior bowing of long bones
HP:0006476	Abnormality of the pancreatic islet cells
HP:0006477	Abnormality of the alveolar ridges
HP:0006479	Abnormality of the dental pulp
HP:0006480	Premature loss of teeth
HP:0006481	Abnormality of primary teeth
HP:0006482	Abnormality of dental morphology
HP:0006483	Abnormal number of teeth
HP:0006485	Agenesis of incisor
HP:0006486	Abnormality of the dental root
HP:0006487	Bowing of the long bones
HP:0006488	Bowing of the arm
HP:0006489	Abnormality of the femoral metaphysis
HP:0006490	Abnormality of lower-limb metaphyses
HP:0006491	Abnormality of the tibial metaphysis
HP:0006492	Aplasia/Hypoplasia of the fibula
HP:0006493	Aplasia/hypoplasia involving bones of the lower limbs
HP:0006494	Aplasia/Hypoplasia involving bones of the feet
HP:0006495	Aplasia/Hypoplasia of the ulna
HP:0006496	Aplasia/hypoplasia involving bones of the upper limbs
HP:0006498	Aplasia/Hypoplasia of the patella
HP:0006499	Abnormality of femoral epiphysis
HP:0006500	Abnormality of lower limb epiphysis morphology
HP:0006501	Aplasia/Hypoplasia of the radius
HP:0006502	Aplasia/Hypoplasia involving the carpal bones
HP:0006503	Aplasia/hypoplasia involving forearm bones
HP:0006504	Anomaly of the limb diaphyses
HP:0006505	Abnormality of limb epiphysis morphology
HP:0006507	Aplasia/hypoplasia of the humerus
HP:0006508	Abnormality of tibial epiphyses
HP:0006509	Diverticulosis of trachea
HP:0006510	Chronic obstructive pulmonary disease
HP:0006511	Laryngeal stridor
HP:0006514	Intraalveolar nodular calcifications
HP:0006515	Interstitial pneumonitis
HP:0006516	Hypersensitivity pneumonitis
HP:0006517	Alveolar proteinosis
HP:0006518	Pulmonary venous occlusion
HP:0006519	Alveolar cell carcinoma
HP:0006520	Progressive pulmonary function impairment
HP:0006521	Pulmonary lymphangiectasia
HP:0006522	Repeated pneumothoraces
HP:0006524	Tracheobronchial leiomyomatosis
HP:0006525	obsolete Lung segmentation defects
HP:0006527	Lymphoid interstitial pneumonia
HP:0006528	Chronic lung disease
HP:0006529	Abnormal pulmonary lymphatics
HP:0006530	Interstitial pulmonary abnormality
HP:0006531	Pleural lymphangiectasia
HP:0006532	Recurrent pneumonia
HP:0006533	Bronchodysplasia
HP:0006535	Recurrent intrapulmonary hemorrhage
HP:0006536	Obstructive lung disease
HP:0006538	Recurrent bronchopulmonary infections
HP:0006539	Bronchial cartilage hypoplasia
HP:0006541	Chronic obstructive airway disease from birth
HP:0006543	Cardiorespiratory arrest
HP:0006544	Extrapulmonary sequestrum
HP:0006548	Pulmonary arteriovenous malformation
HP:0006549	Unilateral primary pulmonary dysgenesis
HP:0006552	Fibrocystic lung disease
HP:0006554	Acute hepatic failure
HP:0006555	Diffuse hepatic steatosis
HP:0006557	Polycystic liver disease
HP:0006558	Decreased mitochondrial complex III activity in liver tissue
HP:0006559	Hepatic calcification
HP:0006560	Biliary hyperplasia
HP:0006561	Lipid accumulation in hepatocytes
HP:0006562	Viral hepatitis
HP:0006563	Malformation of the hepatic ductal plate
HP:0006564	Fluctuating hepatomegaly
HP:0006565	Increased hepatocellular lipid droplets
HP:0006566	Neonatal cholestatic liver disease
HP:0006568	Increased hepatic glycogen content
HP:0006571	Reduced number of intrahepatic bile ducts
HP:0006572	Subacute progressive viral hepatitis
HP:0006573	Acute hepatic steatosis
HP:0006574	Hepatic arteriovenous malformation
HP:0006575	Intrahepatic cholestasis with episodic jaundice
HP:0006576	Hepatic vascular malformations
HP:0006577	Macronodular cirrhosis
HP:0006579	Prolonged neonatal jaundice
HP:0006580	Portal fibrosis
HP:0006581	Depletion of mitochondrial DNA in liver
HP:0006582	Reye syndrome-like episodes
HP:0006583	Fatal liver failure in infancy
HP:0006584	Small abnormally formed scapulae
HP:0006585	Congenital pseudoarthrosis of the clavicle
HP:0006587	Straight clavicles
HP:0006589	Flaring of lower rib cage
HP:0006590	Premature sternal synostosis
HP:0006591	Absent glenoid fossa
HP:0006593	Anomalous rib insertion to vertebrae
HP:0006595	Scapulohumeral synostosis
HP:0006596	Restricted chest movement
HP:0006597	Diaphragmatic paralysis
HP:0006598	Irregular ossification at anterior rib ends
HP:0006599	Medial widening of clavicles
HP:0006600	Progressive calcification of costochondral cartilage
HP:0006603	Flared, irregular rib ends
HP:0006606	Irregular chondrocostal junctions
HP:0006607	Precocious costochondral ossification
HP:0006608	Midclavicular hypoplasia
HP:0006610	Wide intermamillary distance
HP:0006611	Decreased number of sternal ossification centers
HP:0006615	Absent in utero rib ossification
HP:0006619	Anterior rib punctate calcifications
HP:0006623	Costochondral joint sclerosis
HP:0006625	Multifocal breast carcinoma
HP:0006628	Absent sternal ossification
HP:0006631	Hypoplastic distal segments of scapulae
HP:0006633	Glenoid fossa hypoplasia
HP:0006634	Osteosclerosis of ribs
HP:0006637	Sternal punctate calcifications
HP:0006638	Midclavicular aplasia
HP:0006640	Multiple rib fractures
HP:0006641	Prominent floating ribs
HP:0006642	Large sternal ossification centers
HP:0006643	Fused sternal ossification centers
HP:0006644	Thoracic dysplasia
HP:0006645	Thin clavicles
HP:0006646	Costal cartilage calcification
HP:0006647	Congenital microthorax
HP:0006649	Costochondral pain
HP:0006650	Thickening of the lateral border of the scapula
HP:0006655	Rib segmentation abnormalities
HP:0006657	Hypoplasia of first ribs
HP:0006659	Internally rotated shoulders
HP:0006660	Aplastic clavicle
HP:0006665	Coat hanger sign of ribs
HP:0006668	Twelfth rib hypoplasia
HP:0006670	Impaired myocardial contractility
HP:0006671	Paroxysmal atrial tachycardia
HP:0006673	Reduced systolic function
HP:0006677	Prolonged QRS complex
HP:0006679	Granulomatous coronary arteritis
HP:0006681	Absent atrioventricular node
HP:0006682	Ventricular extrasystoles
HP:0006683	Abnormal ventricular filling
HP:0006684	Ventricular preexcitation with multiple accessory pathways
HP:0006685	Endocardial fibrosis
HP:0006687	Aortic tortuosity
HP:0006688	Paroxysmal tachycardia
HP:0006689	Bacterial endocarditis
HP:0006690	Myocardial calcification
HP:0006691	Pulmonic valve myxoma
HP:0006692	Short chordae tendineae of the tricuspid valve
HP:0006693	Myocardial steatosis
HP:0006694	Early progressive calcific cardiac valvular disease
HP:0006695	Atrioventricular canal defect
HP:0006696	Polymorphic and polytopic ventricular extrasystoles
HP:0006698	Dilatation of the ventricular cavity
HP:0006699	Premature atrial contractions
HP:0006702	Coronary artery dissection
HP:0006703	Aplasia/Hypoplasia of the lungs
HP:0006704	Abnormal coronary artery morphology
HP:0006705	Abnormal atrioventricular valve morphology
HP:0006706	Cystic liver disease
HP:0006707	Abnormality of the hepatic vasculature
HP:0006709	Aplasia/Hypoplasia of the nipples
HP:0006710	Aplasia/Hypoplasia of the clavicles
HP:0006711	Aplasia/Hypoplasia involving bones of the thorax
HP:0006712	Aplasia/Hypoplasia of the ribs
HP:0006713	Aplasia/Hypoplasia of the scapulae
HP:0006714	Aplasia/Hypoplasia of the sternum
HP:0006715	Glomus tympanicum paraganglioma
HP:0006716	Hereditary nonpolyposis colorectal carcinoma
HP:0006717	Peripheral neuroepithelioma
HP:0006719	Benign gastrointestinal tract tumors
HP:0006721	Acute lymphoblastic leukemia
HP:0006722	Small intestine carcinoid
HP:0006723	Intestinal carcinoid
HP:0006725	Pancreatic adenocarcinoma
HP:0006727	T-cell acute lymphoblastic leukemias
HP:0006729	Retroperitoneal chemodectomas
HP:0006731	Follicular thyroid carcinoma
HP:0006732	Papillary renal cell carcinoma type 2
HP:0006733	Acute megakaryocytic leukemia
HP:0006735	Renal cortical adenoma
HP:0006737	Extraadrenal pheochromocytoma
HP:0006739	Squamous cell carcinoma of the skin
HP:0006740	Transitional cell carcinoma of the bladder
HP:0006742	Congenital neuroblastoma
HP:0006743	Embryonal rhabdomyosarcoma
HP:0006744	Adrenocortical carcinoma
HP:0006747	Ganglioneuroblastoma
HP:0006748	Adrenal pheochromocytoma
HP:0006749	Malignant gastrointestinal tract tumors
HP:0006751	Paraspinal neurofibromas
HP:0006753	Neoplasm of the stomach
HP:0006755	Cutaneous leiomyosarcoma
HP:0006756	Diffuse leiomyomatosis
HP:0006758	Malignant genitourinary tract tumor
HP:0006762	Renal pelvic carcinoma
HP:0006763	Anal canal squamous carcinoma
HP:0006765	Chondrosarcoma
HP:0006766	Papillary renal cell carcinoma
HP:0006767	Pituitary prolactin cell adenoma
HP:0006768	Localized neuroblastoma
HP:0006769	Myxoid subcutaneous tumors
HP:0006770	Clear cell renal cell carcinoma
HP:0006771	Duodenal adenocarcinoma
HP:0006772	Renal angiomyolipoma
HP:0006773	Cutaneous angiolipomas
HP:0006774	Ovarian papillary adenocarcinoma
HP:0006775	Multiple myeloma
HP:0006778	Benign genitourinary tract neoplasm
HP:0006779	Alveolar rhabdomyosarcoma
HP:0006780	Parathyroid carcinoma
HP:0006781	Hurthle cell thyroid adenoma
HP:0006782	Malignant eosinophil proliferation
HP:0006783	Posterior pharyngeal cleft
HP:0006784	Paranasal sinus hypoplasia
HP:0006785	Limb-girdle muscular dystrophy
HP:0006789	Mitochondrial encephalopathy
HP:0006790	Cerebral cortex with spongiform changes
HP:0006794	Loss of ability to walk in first decade
HP:0006799	Basal ganglia cysts
HP:0006801	Hyperactive deep tendon reflexes
HP:0006802	Abnormal anterior horn cell morphology
HP:0006803	Vivid hallucinations
HP:0006808	Cerebral hypomyelination
HP:0006812	White mater abnormalities in the posterior periventricular region
HP:0006813	Hemiclonic seizures
HP:0006817	Aplasia/Hypoplasia of the cerebellar vermis
HP:0006818	Type I lissencephaly
HP:0006821	Polymicrogyria, anterior to posterior gradient
HP:0006824	Cranial nerve paralysis
HP:0006825	Pallor of dorsal columns of the spinal cord
HP:0006827	Atrophy of the spinal cord
HP:0006829	Severe muscular hypotonia
HP:0006830	obsolete Severe neonatal hypotonia in males
HP:0006834	Developmental stagnation at onset of seizures
HP:0006837	Congenital Horner syndrome
HP:0006844	Absent patellar reflexes
HP:0006846	Acute encephalopathy
HP:0006849	Hypodysplasia of the corpus callosum
HP:0006850	Hypoplasia of the ventral pons
HP:0006851	Symmetric spinal nerve root neurofibromas
HP:0006852	Episodic generalized hypotonia
HP:0006855	Cerebellar vermis atrophy
HP:0006858	Impaired distal proprioception
HP:0006859	Posterior leukoencephalopathy
HP:0006863	Severe expressive language delay
HP:0006865	Sensorimotor polyneuropathy affecting arms more than legs
HP:0006866	Midline central nervous system lipomas
HP:0006870	Lobar holoprosencephaly
HP:0006872	Cerebral hypoplasia
HP:0006873	Symmetrical progressive peripheral demyelination
HP:0006877	obsolete Mental retardation, in some
HP:0006879	Pontocerebellar atrophy
HP:0006880	Cerebellar hemangioblastoma
HP:0006881	Diffuse peripheral demyelination
HP:0006882	Severe hydrocephalus
HP:0006886	Impaired distal vibration sensation
HP:0006887	Intellectual disability, progressive
HP:0006888	Meningoencephalocele
HP:0006889	Intellectual disability, borderline
HP:0006891	Thick cerebral cortex
HP:0006892	Frontotemporal cerebral atrophy
HP:0006893	Severely dysplastic cerebellum
HP:0006894	Hypoplastic olfactory lobes
HP:0006895	Lower limb hypertonia
HP:0006896	Hypnopompic hallucinations
HP:0006897	Cranial nerve VI palsy
HP:0006899	Fusion of the cerebellar hemispheres
HP:0006901	Impaired thermal sensitivity
HP:0006903	Congenital peripheral neuropathy
HP:0006904	Late-onset spinocerebellar degeneration
HP:0006906	Congenital intracerebral calcification
HP:0006913	Frontal cortical atrophy
HP:0006915	Inability to walk by childhood/adolescence
HP:0006916	Intraaxonal accumulation of curvilinear autofluorescent lipopigment storage material
HP:0006918	Diffuse cerebral sclerosis
HP:0006919	Abnormal aggressive, impulsive or violent behavior
HP:0006921	Axial muscle stiffness
HP:0006926	Metachromatic leukodystrophy variant
HP:0006927	Unilateral polymicrogyria
HP:0006929	Hypoglycemic encephalopathy
HP:0006930	Frontoparietal cortical dysplasia
HP:0006931	Lipoma of corpus callosum
HP:0006932	Transient psychotic episodes
HP:0006934	Congenital nystagmus
HP:0006937	Impaired distal tactile sensation
HP:0006938	Impaired vibration sensation at ankles
HP:0006943	Diffuse spongiform leukoencephalopathy
HP:0006944	Abolished vibration sense
HP:0006946	Recurrent meningitis
HP:0006949	Episodic peripheral neuropathy
HP:0006951	Retrocerebellar cyst
HP:0006955	Olivopontocerebellar hypoplasia
HP:0006956	Dilation of lateral ventricles
HP:0006957	Loss of ability to walk
HP:0006958	Abnormal auditory evoked potentials
HP:0006959	Proximal spinal muscular atrophy
HP:0006960	Choroid plexus calcification
HP:0006961	Jerky head movements
HP:0006962	Gait instability, worse in the dark
HP:0006964	Cerebral cortical neurodegeneration
HP:0006965	Acute necrotizing encephalopathy
HP:0006970	Periventricular leukomalacia
HP:0006976	Necrotizing encephalopathy
HP:0006977	Grammar-specific speech disorder
HP:0006978	Dysmyelinating leukodystrophy
HP:0006979	Sleep-wake cycle disturbance
HP:0006980	Progressive leukoencephalopathy
HP:0006983	Slowly progressive spastic quadriparesis
HP:0006984	Distal sensory loss of all modalities
HP:0006986	Upper limb spasticity
HP:0006988	Alobar holoprosencephaly
HP:0006989	Dysplastic corpus callosum
HP:0006990	Myelin-dependent gliosis
HP:0006992	Anterior basal encephalocele
HP:0006994	Diffuse leukoencephalopathy
HP:0006999	Basal ganglia gliosis
HP:0007000	Morning myoclonic jerks
HP:0007001	Loss of Purkinje cells in the cerebellar vermis
HP:0007002	Motor axonal neuropathy
HP:0007006	Dorsal column degeneration
HP:0007007	Cavitation of the basal ganglia
HP:0007009	Central nervous system degeneration
HP:0007010	Poor fine motor coordination
HP:0007011	Fourth cranial nerve palsy
HP:0007015	Poor gross motor coordination
HP:0007016	Corticospinal tract hypoplasia
HP:0007017	Progressive forgetfulness
HP:0007018	Attention deficit hyperactivity disorder
HP:0007020	Progressive spastic paraplegia
HP:0007021	Pain insensitivity
HP:0007023	Antenatal intracerebral hemorrhage
HP:0007024	Pseudobulbar paralysis
HP:0007027	Poorly formed metencephalon
HP:0007029	Cerebral berry aneurysm
HP:0007030	Nonprogressive encephalopathy
HP:0007033	Cerebellar dysplasia
HP:0007034	Generalized hyperreflexia
HP:0007035	Anterior encephalocele
HP:0007036	Hypoplasia of olfactory tract
HP:0007039	Symmetric lesions of the basal ganglia
HP:0007041	Chronic lymphocytic meningitis
HP:0007042	Focal white matter lesions
HP:0007045	Midline brain calcifications
HP:0007047	Atrophy of the dentate nucleus
HP:0007048	Large basal ganglia
HP:0007052	Multifocal cerebral white matter abnormalities
HP:0007054	Hyperreflexia proximally
HP:0007057	Poor hand-eye coordination
HP:0007058	Generalized cerebral atrophy/hypoplasia
HP:0007063	Aplasia of the inferior half of the cerebellar vermis
HP:0007064	Progressive language deterioration
HP:0007065	Disorganization of the anterior cerebellar vermis
HP:0007066	Proximal limb muscle stiffness
HP:0007067	Distal peripheral sensory neuropathy
HP:0007068	Inferior vermis hypoplasia
HP:0007069	Profound static encephalopathy
HP:0007074	Thick corpus callosum
HP:0007076	Extrapyramidal muscular rigidity
HP:0007078	Decreased amplitude of sensory action potentials
HP:0007081	Late-onset muscular dystrophy
HP:0007082	Dilated third ventricle
HP:0007083	Hyperactive patellar reflex
HP:0007086	Social and occupational deterioration
HP:0007087	obsolete Involuntary jerking movements
HP:0007089	Facial-lingual fasciculations
HP:0007095	Frontoparietal polymicrogyria
HP:0007096	Hypoplasia of the optic tract
HP:0007097	Cranial nerve motor loss
HP:0007098	Paroxysmal choreoathetosis
HP:0007099	Arnold-Chiari type I malformation
HP:0007100	Progressive ventriculomegaly
HP:0007103	Hypointensity of cerebral white matter on MRI
HP:0007104	Prolonged somatosensory evoked potentials
HP:0007105	Infantile encephalopathy
HP:0007107	Segmental peripheral demyelination
HP:0007108	Demyelinating peripheral neuropathy
HP:0007109	Periventricular cysts
HP:0007110	Central hypoventilation
HP:0007111	Chronic hepatic encephalopathy
HP:0007112	Temporal cortical atrophy
HP:0007115	Orbital encephalocele
HP:0007117	Corticospinal tract atrophy
HP:0007123	Subcortical dementia
HP:0007126	Proximal amyotrophy
HP:0007129	Cerebellar medulloblastoma
HP:0007131	Acute demyelinating polyneuropathy
HP:0007132	Pallidal degeneration
HP:0007133	Progressive peripheral neuropathy
HP:0007141	Sensorimotor neuropathy
HP:0007146	Bilateral basal ganglia lesions
HP:0007149	Distal upper limb amyotrophy
HP:0007153	Progressive extrapyramidal movement disorder
HP:0007156	Asymmetric limb muscle stiffness
HP:0007158	Progressive extrapyramidal muscular rigidity
HP:0007159	Fluctuations in consciousness
HP:0007162	Diffuse demyelination of the cerebral white matter
HP:0007163	obsolete Corticospinal tract disease in lower limbs
HP:0007164	Slowed slurred speech
HP:0007165	Periventricular gray matter heterotopia
HP:0007166	Paroxysmal dyskinesia
HP:0007178	Motor polyneuropathy
HP:0007179	Absent smooth pursuit
HP:0007181	Interosseus muscle atrophy
HP:0007182	Peripheral hypomyelination
HP:0007183	Focal T2 hyperintense basal ganglia lesion
HP:0007185	Loss of consciousness
HP:0007187	Focal lissencephaly
HP:0007188	Congenital facial diplegia
HP:0007190	Neuronal loss in the cerebral cortex
HP:0007193	Generalized tonic-clonic seizures on awakening
HP:0007199	Progressive spastic paraparesis
HP:0007200	Episodic hypersomnia
HP:0007201	Cerebral artery atherosclerosis
HP:0007204	Diffuse white matter abnormalities
HP:0007206	Hemimegalencephaly
HP:0007207	Photosensitive tonic-clonic seizures
HP:0007208	Irregular myelin loops
HP:0007209	Facial paralysis
HP:0007210	Lower limb amyotrophy
HP:0007215	Periodic hyperkalemic paralysis
HP:0007220	Demyelinating motor neuropathy
HP:0007221	Progressive truncal ataxia
HP:0007227	Macrogyria
HP:0007229	Intracerebral periventricular calcifications
HP:0007230	Decreased distal sensory nerve action potential
HP:0007232	Spinocerebellar tract disease in lower limbs
HP:0007233	Clusters of axonal regeneration
HP:0007236	Recurrent subcortical infarcts
HP:0007238	Nonarteriosclerotic cerebral calcification
HP:0007239	Congenital encephalopathy
HP:0007240	Progressive gait ataxia
HP:0007249	Decreased number of small peripheral myelinated nerve fibers
HP:0007250	Recurrent external ophthalmoplegia
HP:0007256	Abnormal pyramidal sign
HP:0007258	Severe demyelination of the white matter
HP:0007260	Type II lissencephaly
HP:0007262	Symmetric peripheral demyelination
HP:0007263	Spinocerebellar atrophy
HP:0007265	Absent mesencephalon
HP:0007266	Cerebral dysmyelination
HP:0007267	Chronic axonal neuropathy
HP:0007268	Aprosencephaly
HP:0007269	Spinal muscular atrophy
HP:0007270	Atypical absence seizure
HP:0007271	Occipital myelomeningocele
HP:0007272	Progressive psychomotor deterioration
HP:0007274	Recurrent bacterial meningitis
HP:0007277	Paucity of anterior horn motor neurons
HP:0007280	Acute infantile spinal muscular atrophy
HP:0007281	Developmental stagnation
HP:0007285	Facial palsy secondary to cranial hyperostosis
HP:0007286	Horizontal jerk nystagmus
HP:0007289	Limb fasciculations
HP:0007291	Posterior fossa cyst
HP:0007293	Anterior sacral meningocele
HP:0007295	Chaotic rapid conjugate ocular movements
HP:0007299	Dysfunction of lateral corticospinal tracts
HP:0007301	Oromotor apraxia
HP:0007302	Bipolar affective disorder
HP:0007305	CNS demyelination
HP:0007307	Rapid neurologic deterioration
HP:0007308	Extrapyramidal dyskinesia
HP:0007311	Short stepped shuffling gait
HP:0007313	Cerebral degeneration
HP:0007314	White matter neuronal heterotopia
HP:0007316	obsolete Involuntary writhing movements
HP:0007321	Deep white matter hypodensities
HP:0007325	Generalized dystonia
HP:0007326	Progressive choreoathetosis
HP:0007327	Mixed demyelinating and axonal polyneuropathy
HP:0007328	Impaired pain sensation
HP:0007330	Frontal encephalocele
HP:0007332	Hemifacial seizures
HP:0007333	Hypoplasia of the frontal lobes
HP:0007334	Generalized tonic-clonic seizures with focal onset
HP:0007335	Recurrent encephalopathy
HP:0007338	Hypermetric saccades
HP:0007340	Lower limb muscle weakness
HP:0007341	Diffuse swelling of cerebral white matter
HP:0007343	Abnormal morphology of the limbic system
HP:0007344	Atrophy/Degeneration involving the spinal cord
HP:0007346	Subcortical white matter calcifications
HP:0007348	Hypoplasia of the pyramidal tract
HP:0007350	Hyperreflexia in upper limbs
HP:0007351	Upper limb postural tremor
HP:0007352	Cerebellar calcifications
HP:0007354	Amyotrophic lateral sclerosis
HP:0007359	Focal-onset seizure
HP:0007360	Aplasia/Hypoplasia of the cerebellum
HP:0007361	Abnormality of the pons
HP:0007362	Aplasia/Hypoplasia of the brainstem
HP:0007363	Aplasia/Hypoplasia of the pyramidal tract
HP:0007364	Aplasia/Hypoplasia of the cerebrum
HP:0007365	Aplasia/Hypoplasia involving the corticospinal tracts
HP:0007366	Atrophy/Degeneration affecting the brainstem
HP:0007367	Atrophy/Degeneration affecting the central nervous system
HP:0007369	Atrophy/Degeneration affecting the cerebrum
HP:0007370	Aplasia/Hypoplasia of the corpus callosum
HP:0007371	Corpus callosum atrophy
HP:0007372	Atrophy/Degeneration involving the corticospinal tracts
HP:0007373	Motor neuron atrophy
HP:0007374	Atrophy/Degeneration involving the caudate nucleus
HP:0007375	Abnormality of the septum pellucidum
HP:0007376	Abnormality of the choroid plexus
HP:0007377	Abnormality of somatosensory evoked potentials
HP:0007378	Neoplasm of the gastrointestinal tract
HP:0007379	Neoplasm of the genitourinary tract
HP:0007380	Facial telangiectasia
HP:0007381	Congenital exfoliative erythroderma
HP:0007383	Congenital localized absence of skin
HP:0007384	Aberrant melanosome maturation
HP:0007385	Aplasia cutis congenita of scalp
HP:0007387	Hypoplastic sweat glands
HP:0007390	Hyperkeratosis with erythema
HP:0007392	Excessive wrinkled skin
HP:0007394	Prominent superficial blood vessels
HP:0007395	Postnatal-onset ichthyosiform erythroderma
HP:0007396	Early cutaneous photosensitivity
HP:0007397	Axillary apocrine gland hypoplasia
HP:0007398	Asymmetric, linear skin defects
HP:0007400	Irregular hyperpigmentation
HP:0007401	Macular atrophy
HP:0007402	Areas of hypopigmentation and hyperpigmentation that do not follow Blaschko lines
HP:0007403	Hypertrophy of skin of soles
HP:0007404	Nonepidermolytic palmoplantar keratoderma
HP:0007406	Hyperpigmentation of eyelids
HP:0007407	Excessive skin wrinkling on dorsum of hands and fingers
HP:0007408	Tegumentary leishmaniasis susceptibility
HP:0007409	obsolete Absence of subcutaneous fat over entire body except buttocks, hips, and thighs
HP:0007410	Palmoplantar hyperhidrosis
HP:0007411	Hypoplastic-absent sebaceous glands
HP:0007412	Macular hyperpigmented dermopathy
HP:0007413	Nevus flammeus of the forehead
HP:0007414	Neonatal wrinkled skin of hands and feet
HP:0007417	Discoid lupus rash
HP:0007418	Alopecia totalis
HP:0007420	Spontaneous hematomas
HP:0007421	Telangiectases of the cheeks
HP:0007425	Hyperextensible skin of face
HP:0007427	Reticulated skin pigmentation
HP:0007428	Telangiectasia of the oral mucosa
HP:0007429	Few cafe-au-lait spots
HP:0007430	Generalized edema
HP:0007431	Congenital ichthyosiform erythroderma
HP:0007432	Intermittent generalized erythematous papular rash
HP:0007434	Plaque-like facial hemangioma
HP:0007435	Diffuse palmoplantar keratoderma
HP:0007436	Hair-nail ectodermal dysplasia
HP:0007437	Multiple cutaneous leiomyomas
HP:0007438	Mottled pigmentation of the trunk and proximal extremities
HP:0007439	Generalized keratosis follicularis
HP:0007440	Generalized hyperpigmentation
HP:0007441	Hyperpigmented/hypopigmented macules
HP:0007443	Partial albinism
HP:0007446	Palmoplantar blistering
HP:0007447	Diffuse palmoplantar hyperkeratosis
HP:0007448	Hyperkeratosis over edematous areas
HP:0007449	Confetti-like hypopigmented macules
HP:0007450	Increased groin pigmentation with raindrop depigmentation
HP:0007451	Ipsilateral lack of facial sweating
HP:0007452	Midface capillary hemangioma
HP:0007453	Flexural lichenification
HP:0007455	Adermatoglyphia
HP:0007456	Progressive reticulate hyperpigmentation
HP:0007457	Prominent veins on trunk
HP:0007458	Focal hyperextensible skin
HP:0007459	Generalized anhidrosis
HP:0007460	Autoamputation of digits
HP:0007461	Hemangiomatosis
HP:0007462	Bitot spots of the conjunctiva
HP:0007464	Sparse facial hair
HP:0007465	Honeycomb palmoplantar keratoderma
HP:0007466	Midfrontal capillary hemangioma
HP:0007468	Perifollicular hyperkeratosis
HP:0007469	Palmoplantar cutis gyrata
HP:0007470	Periarticular subcutaneous nodules
HP:0007471	Axillary and groin hyperpigmentation and hypopigmentation
HP:0007473	Crusting erythematous dermatitis
HP:0007475	Congenital bullous ichthyosiform erythroderma
HP:0007476	Anhidrotic ectodermal dysplasia
HP:0007477	Abnormal dermatoglyphics
HP:0007479	Congenital nonbullous ichthyosiform erythroderma
HP:0007480	Decreased sweating due to autonomic dysfunction
HP:0007481	Hyperpigmented nevi
HP:0007482	Generalized papillary lesions
HP:0007483	Depigmentation/hyperpigmentation of skin
HP:0007485	Absence of subcutaneous fat
HP:0007486	Cavernous hemangioma of the face
HP:0007488	Diffuse skin atrophy
HP:0007489	Diffuse telangiectasia
HP:0007490	Linear arrays of macular hyperkeratoses in flexural areas
HP:0007494	Discrete 2 to 5-mm hyper- and hypopigmented macules
HP:0007495	Prematurely aged appearance
HP:0007497	Focal friction-related palmoplantar hyperkeratosis
HP:0007499	Recurrent staphylococcal infections
HP:0007500	Decreased number of sweat glands
HP:0007501	Streaks of hyperkeratosis along each finger onto the palm
HP:0007502	Follicular hyperkeratosis
HP:0007503	Generalized ichthyosis
HP:0007504	Diffuse slow skin atrophy
HP:0007505	Progressive hyperpigmentation
HP:0007506	Congenital absence of skin of limbs
HP:0007508	Punctate palmar hyperkeratosis
HP:0007509	Patchy hypo- and hyperpigmentation
HP:0007510	Focal dermal aplasia/hypoplasia
HP:0007511	Mottled pigmentation of photoexposed areas
HP:0007513	Generalized hypopigmentation
HP:0007514	Edema of the dorsum of hands
HP:0007515	Hypoplastic pilosebaceous units
HP:0007516	Redundant skin on fingers
HP:0007517	Palmoplantar cutis laxa
HP:0007519	Lack of subcutaneous fatty tissue
HP:0007521	Irregular hyperpigmentation of back
HP:0007522	Increased number of skin folds
HP:0007524	Atypical neurofibromatosis
HP:0007525	Yellow subcutaneous tissue covered by thin, scaly skin
HP:0007526	Hypopigmented skin patches on arms
HP:0007529	Hidrotic ectodermal dysplasia
HP:0007530	Punctate palmoplantar hyperkeratosis
HP:0007534	Congenital posterior occipital alopecia
HP:0007535	Hypopigmented streaks
HP:0007536	Aplasia cutis congenita of midline scalp vertex
HP:0007537	Severe photosensitivity
HP:0007541	Frontal cutaneous lipoma
HP:0007542	Absent pigmentation of the ventral chest
HP:0007543	Epidermal hyperkeratosis
HP:0007544	Piebaldism
HP:0007545	Congenital palmoplantar keratosis
HP:0007546	Linear hyperpigmentation
HP:0007548	Palmoplantar keratosis with erythema and scale
HP:0007549	Desquamation of skin soon after birth
HP:0007550	Hypohidrosis or hyperhidrosis
HP:0007552	Abnormal subcutaneous fat tissue distribution
HP:0007553	Congenital symmetrical palmoplantar keratosis
HP:0007554	Confetti hypopigmentation pattern of lower leg skin
HP:0007556	Plantar hyperkeratosis
HP:0007559	Localized epidermolytic hyperkeratosis
HP:0007560	Unusual dermatoglyphics
HP:0007561	Telangiectases in sun-exposed and nonexposed skin
HP:0007565	Multiple cafe-au-lait spots
HP:0007566	Index finger dermatoglyphic radial loop
HP:0007569	Generalized seborrheic dermatitis
HP:0007570	Hyperkeratosis lenticularis perstans
HP:0007572	Hyperpigmented streaks
HP:0007573	Late onset atopic dermatitis
HP:0007574	Generalized bronze hyperpigmentation
HP:0007576	Palmar neurofibromas
HP:0007581	Mediosternal, longitudinal streak of hypopigmentation
HP:0007583	Telangiectasia macularis eruptiva perstans
HP:0007585	Skin fragility with non-scarring blistering
HP:0007586	Telangiectases producing 'marbled' skin
HP:0007587	Numerous pigmented freckles
HP:0007588	Reticular hyperpigmentation
HP:0007589	Aplasia cutis congenita on trunk or limbs
HP:0007590	Aplasia cutis congenita over posterior parietal area
HP:0007592	Aplasia/Hypoplastia of the eccrine sweat glands
HP:0007595	Redundant skin in infancy
HP:0007596	Painful subcutaneous lipomas
HP:0007597	Congenital palmoplantar keratodermia
HP:0007598	Bilateral single transverse palmar creases
HP:0007599	Generalized reticulate brown pigmentation
HP:0007601	Midline facial capillary hemangioma
HP:0007602	Complex palmar dermatoglyphic pattern
HP:0007603	Freckles in sun-exposed areas
HP:0007605	Excessive wrinkling of palmar skin
HP:0007606	Multiple cutaneous malignancies
HP:0007607	Hypohidrotic ectodermal dysplasia
HP:0007608	Abnormal palmar dermal ridges
HP:0007609	Hypoproteinemic edema
HP:0007610	Blotching pigmentation of the skin
HP:0007613	Spinous keratoses of palms and soles
HP:0007616	Nevus flammeus nuchae
HP:0007617	Fine, reticulate skin pigmentation
HP:0007618	Subcutaneous calcification
HP:0007620	Cutaneous leiomyoma
HP:0007621	Telangiectasia of extensor surfaces
HP:0007623	Pigmentation anomalies of sun-exposed skin
HP:0007626	Mandibular osteomyelitis
HP:0007627	Mandibular condyle aplasia
HP:0007628	Mandibular condyle hypoplasia
HP:0007633	Bilateral microphthalmos
HP:0007634	Nonarteritic anterior ischemic optic neuropathy
HP:0007641	Dyschromatopsia
HP:0007642	Congenital stationary night blindness
HP:0007643	Peripheral tractional retinal detachment
HP:0007646	Absent lower eyelashes
HP:0007647	Congenital extraocular muscle anomaly
HP:0007648	Punctate cataract
HP:0007649	Congenital hypertrophy of retinal pigment epithelium
HP:0007650	Progressive ophthalmoplegia
HP:0007651	Ectropion of lower eyelids
HP:0007654	obsolete Retinal striation
HP:0007655	Eversion of lateral third of lower eyelids
HP:0007656	Lacrimal gland aplasia
HP:0007657	Diffuse nuclear cataract
HP:0007658	Large hyperpigmented retinal spots
HP:0007659	obsolete Decreased retinal pigmentation with dispersion
HP:0007661	Abnormality of chorioretinal pigmentation
HP:0007663	Reduced visual acuity
HP:0007665	Curly eyelashes
HP:0007667	Peripheral cystoid retinal degeneration
HP:0007668	Impaired pursuit initiation and maintenance
HP:0007670	Abnormal vestibulo-ocular reflex
HP:0007675	Progressive night blindness
HP:0007676	Hypoplasia of the iris
HP:0007677	Vitelliform-like macular lesions
HP:0007678	Lacrimal duct stenosis
HP:0007680	Depigmented fundus
HP:0007685	Peripheral retinal avascularization
HP:0007686	Abnormal pupillary function
HP:0007687	Unilateral ptosis
HP:0007688	Undetectable light- and dark-adapted electroretinogram
HP:0007690	Map-dot-fingerprint corneal dystrophy
HP:0007691	obsolete Short curly eyelashes
HP:0007692	obsolete Nonnuclear polymorphic congenital cataract
HP:0007695	Abnormal pupillary light reflex
HP:0007697	Hypoplasia of the lower eyelids
HP:0007698	obsolete Retinal pigment epithelial atrophy
HP:0007700	Anterior segment developmental abnormality
HP:0007702	obsolete Pigmentary retinal deposits
HP:0007703	Abnormality of retinal pigmentation
HP:0007704	Paroxysmal involuntary eye movements
HP:0007705	Corneal degeneration
HP:0007707	Congenital aphakia
HP:0007708	Absent inner eyelashes
HP:0007709	Band-shaped corneal dystrophy
HP:0007710	Peripheral vitreous opacities
HP:0007712	obsolete Choroidal dystrophy
HP:0007713	obsolete Juvenile zonular cataracts
HP:0007715	Weak extraocular muscles
HP:0007716	Uveal melanoma
HP:0007717	Chronic irritative conjunctivitis
HP:0007720	Flat cornea
HP:0007721	Saccular conjunctival dilatations
HP:0007722	Retinal pigment epithelial atrophy
HP:0007727	Opacification of the corneal epithelium
HP:0007728	Congenital miosis
HP:0007730	Iris hypopigmentation
HP:0007731	Chorioretinal dysplasia
HP:0007732	Lacrimal gland hypoplasia
HP:0007733	Laterally curved eyebrow
HP:0007734	Enlarged lacrimal glands
HP:0007736	obsolete Pericentral retinal dystrophy
HP:0007737	Bone spicule pigmentation of the retina
HP:0007738	Uncontrolled eye movements
HP:0007739	obsolete Mildly reduced visual acuity
HP:0007740	Long eyelashes in irregular rows
HP:0007744	obsolete Iridoretinal coloboma
HP:0007747	Monocular horizontal nystagmus
HP:0007748	obsolete Irido-fundal coloboma
HP:0007750	Hypoplasia of the fovea
HP:0007754	Macular dystrophy
HP:0007755	Juvenile epithelial corneal dystrophy
HP:0007756	obsolete Slitlike anterior chamber angles in children
HP:0007757	obsolete Hypoplasia of choroid
HP:0007758	obsolete Congenital visual impairment
HP:0007759	Opacification of the corneal stroma
HP:0007760	Crystalline corneal dystrophy
HP:0007761	Pericentral scotoma
HP:0007763	Retinal telangiectasia
HP:0007765	Deep anterior chamber
HP:0007766	Optic disc hypoplasia
HP:0007768	Central retinal vessel vascular tortuosity
HP:0007769	Peripheral retinal degeneration
HP:0007770	Hypoplasia of the retina
HP:0007772	Impaired smooth pursuit
HP:0007773	Vitreoretinopathy
HP:0007774	Hypoplasia of the ciliary body
HP:0007776	Sparse lower eyelashes
HP:0007777	Chorioretinal scar
HP:0007778	Posterior retinal neovascularization
HP:0007779	Anterior segment of eye aplasia
HP:0007780	Cortical pulverulent cataract
HP:0007782	obsolete Peripheral retinal cone degeneration
HP:0007783	obsolete Butterfly retinal pigment epithelial dystrophy
HP:0007786	obsolete Lacunar retinal depigmentation
HP:0007787	Posterior subcapsular cataract
HP:0007791	Patchy atrophy of the retinal pigment epithelium
HP:0007792	Microsaccadic pursuit
HP:0007793	Granular macular appearance
HP:0007795	Anterior cortical cataract
HP:0007797	Retinal vascular malformation
HP:0007798	obsolete Foveal dystrophy
HP:0007799	Conjunctival whitish salt-like deposits
HP:0007800	Increased axial length of the globe
HP:0007801	obsolete Fishnet retinal pigmentation
HP:0007802	Granular corneal dystrophy
HP:0007803	Monochromacy
HP:0007807	Optic nerve compression
HP:0007808	obsolete Bilateral retinal coloboma
HP:0007809	Punctate corneal dystrophy
HP:0007810	obsolete Progressive bifocal chorioretinal atrophy
HP:0007811	Horizontal pendular nystagmus
HP:0007812	Herpetiform corneal ulceration
HP:0007813	Nongranulomatous uveitis
HP:0007814	Retinal pigment epithelial mottling
HP:0007815	Abnormal distribution of retinal arterioles and venules
HP:0007817	Horizontal supranuclear gaze palsy
HP:0007818	Central heterochromia
HP:0007819	Presenile cataracts
HP:0007820	Lacrimal punctal atresia
HP:0007822	Central retinal exudate
HP:0007824	Total ophthalmoplegia
HP:0007825	obsolete Cataracts develop in second or third decade
HP:0007827	Nodular corneal dystrophy
HP:0007829	obsolete Diffuse retinal cone degeneration
HP:0007830	Adult-onset night blindness
HP:0007831	Nonprogressive restrictive external ophthalmoplegia
HP:0007832	Pigmentation of the sclera
HP:0007833	Anterior chamber synechiae
HP:0007834	Progressive cataract
HP:0007835	S-shaped palpebral fissures
HP:0007836	Mosaic corneal dystrophy
HP:0007838	Progressive ptosis
HP:0007840	Long upper eyelashes
HP:0007841	Amyloid deposition in the vitreous humor
HP:0007843	Attenuation of retinal blood vessels
HP:0007850	Retinal vascular proliferation
HP:0007851	obsolete Temporal displacement of maculae
HP:0007852	obsolete Pericentral pigmentary retinopathy
HP:0007854	Glaucomatous visual field defect
HP:0007856	Punctate opacification of the cornea
HP:0007858	Chorioretinal lacunae
HP:0007859	Congenital horizontal nystagmus
HP:0007862	Retinal calcification
HP:0007866	Retinal infarction
HP:0007867	Restrictive partial external ophthalmoplegia
HP:0007868	obsolete Age-related macular degeneration
HP:0007869	obsolete Peripheral retinopathy
HP:0007872	Choroidal hemangioma
HP:0007873	Abnormally prominent line of Schwalbe
HP:0007874	Almond-shaped palpebral fissure
HP:0007875	Congenital blindness
HP:0007876	obsolete Juvenile cortical cataract
HP:0007879	Allergic conjunctivitis
HP:0007880	Marginal corneal dystrophy
HP:0007881	Central corneal dystrophy
HP:0007885	Slowed horizontal saccades
HP:0007886	Absent extraocular muscles
HP:0007889	Iridescent posterior subcapsular cataract
HP:0007892	Hypoplasia of the lacrimal punctum
HP:0007893	obsolete Progressive retinal degeneration
HP:0007894	Hypopigmentation of the fundus
HP:0007898	Exudative retinopathy
HP:0007899	Retinal nonattachment
HP:0007900	Hypoplastic lacrimal duct
HP:0007901	obsolete Retinal malformation
HP:0007902	Vitreous hemorrhage
HP:0007903	Paravenous chorioretinal atrophy
HP:0007905	Abnormal iris vasculature
HP:0007906	Ocular hypertension
HP:0007910	obsolete Nonprogressive congenital retinal dystrophy
HP:0007911	Congenital bilateral ptosis
HP:0007913	Reticular retinal dystrophy
HP:0007915	Polymorphous posterior corneal dystrophy
HP:0007916	obsolete Small anterior lens surface opacities
HP:0007917	Tractional retinal detachment
HP:0007920	obsolete Congenital chorioretinal dystrophy
HP:0007922	Hypermyelinated retinal nerve fibers
HP:0007923	obsolete Foveal hyperplasia
HP:0007924	Slow decrease in visual acuity
HP:0007925	Lacrimal duct aplasia
HP:0007928	Abnormal flash visual evoked potentials
HP:0007929	Peripheral retinal detachment
HP:0007930	obsolete Prominent epicanthal folds
HP:0007932	Bilateral congenital mydriasis
HP:0007933	Broad lateral eyebrow
HP:0007935	Juvenile posterior subcapsular lenticular opacities
HP:0007936	Restrictive external ophthalmoplegia
HP:0007937	Reticular pigmentary degeneration
HP:0007939	Blue cone monochromacy
HP:0007941	Limited extraocular movements
HP:0007942	Internal ophthalmoplegia
HP:0007943	Congenital stapes ankylosis
HP:0007944	Intermittent microsaccadic pursuits
HP:0007945	obsolete Choroidal degeneration
HP:0007946	Unilateral narrow palpebral fissure
HP:0007947	Pericentral retinitis pigmentosa
HP:0007948	Dense posterior cortical cataract
HP:0007949	obsolete Progressive macular scarring
HP:0007950	Peripapillary chorioretinal atrophy
HP:0007956	obsolete Bilateral choroid coloboma
HP:0007957	Corneal opacity
HP:0007958	Optic atrophy from cranial nerve compression
HP:0007961	obsolete Rarefaction of retinal pigmentation
HP:0007962	Speckled corneal dystrophy
HP:0007963	Pattern dystrophy of the retina
HP:0007964	Degenerative vitreoretinopathy
HP:0007965	Undetectable visual evoked potentials
HP:0007968	Remnants of the hyaloid vascular system
HP:0007970	Congenital ptosis
HP:0007971	Lamellar cataract
HP:0007973	Retinal dysplasia
HP:0007975	Hypometric horizontal saccades
HP:0007976	Cerulean cataract
HP:0007979	Gaze-evoked horizontal nystagmus
HP:0007980	Absent retinal pigment epithelium
HP:0007981	obsolete Concentric narrowing of visual field
HP:0007982	obsolete Central tapetoretinal dystrophy
HP:0007984	Electronegative electroretinogram
HP:0007985	Retinal arteriolar occlusion
HP:0007986	Increased retinal vascularity
HP:0007987	Progressive visual field defects
HP:0007988	Macular hypopigmentation
HP:0007989	Intraretinal exudate
HP:0007990	Hypoplastic iris stroma
HP:0007992	Lattice retinal degeneration
HP:0007993	Malformed lacrimal duct
HP:0007994	Peripheral visual field loss
HP:0008000	Decreased corneal reflex
HP:0008001	Foveal hyperpigmentation
HP:0008002	Abnormality of macular pigmentation
HP:0008003	Jerky ocular pursuit movements
HP:0008005	Congenital corneal dystrophy
HP:0008007	Primary congenital glaucoma
HP:0008008	obsolete Progressive central visual loss
HP:0008009	Three rows of eyelashes
HP:0008011	Peripheral opacification of the cornea
HP:0008012	obsolete Congenital myopia
HP:0008014	Central fundal arteriolar microaneurysms
HP:0008017	obsolete Depigmented lesions of the retinal pigment epithelium
HP:0008019	Superior lens subluxation
HP:0008020	Cone dystrophy
HP:0008024	obsolete Congenital nuclear cataract
HP:0008026	Horizontal opticokinetic nystagmus
HP:0008028	Cystoid macular degeneration
HP:0008030	Retinal arteritis
HP:0008031	Posterior Y-sutural cataract
HP:0008033	obsolete Congenital exotropia
HP:0008034	Abnormal iris pigmentation
HP:0008035	Retinitis pigmentosa inversa
HP:0008036	obsolete Rod-cone dystrophy
HP:0008037	Absent anterior chamber of the eye
HP:0008038	Aplastic/hypoplastic lacrimal glands
HP:0008039	Subepithelial corneal opacities
HP:0008041	Late onset congenital glaucoma
HP:0008043	Retinal arteriolar constriction
HP:0008045	Enlarged flash visual evoked potentials
HP:0008046	Abnormality of the retinal vasculature
HP:0008047	Abnormality of the vasculature of the eye
HP:0008048	Abnormality of the line of Schwalbe
HP:0008049	Abnormality of the extraocular muscles
HP:0008050	Abnormality of the palpebral fissures
HP:0008051	obsolete Abnormality of the retinal pigment epithelium
HP:0008052	Retinal fold
HP:0008053	Aplasia/Hypoplasia of the iris
HP:0008054	Abnormal vasculature of the conjunctiva morphology
HP:0008055	Aplasia/Hypoplasia affecting the uvea
HP:0008056	Aplasia/Hypoplasia affecting the eye
HP:0008057	Aplasia/Hypoplasia affecting the fundus
HP:0008058	Aplasia/Hypoplasia of the optic nerve
HP:0008059	Aplasia/Hypoplasia of the macula
HP:0008060	Aplasia/Hypoplasia of the fovea
HP:0008061	Aplasia/Hypoplasia of the retina
HP:0008062	Aplasia/Hypoplasia affecting the anterior segment of the eye
HP:0008063	Aplasia/Hypoplasia of the lens
HP:0008064	Ichthyosis
HP:0008065	Aplasia/Hypoplasia of the skin
HP:0008066	Abnormal blistering of the skin
HP:0008067	Abnormally lax or hyperextensible skin
HP:0008069	Neoplasm of the skin
HP:0008070	Sparse hair
HP:0008071	Maternal hypertension
HP:0008072	Maternal virilization in pregnancy
HP:0008073	Low maternal serum estriol
HP:0008074	Metatarsal periosteal thickening
HP:0008075	Progressive pes cavus
HP:0008076	Osteoporotic tarsals
HP:0008078	Thin metatarsal cortices
HP:0008079	Absent fifth metatarsal
HP:0008080	Hallux varus
HP:0008081	Pes valgus
HP:0008082	Medial deviation of the foot
HP:0008083	2nd-5th toe middle phalangeal hypoplasia
HP:0008087	Nonossified fifth metatarsal
HP:0008089	Abnormality of the fifth metatarsal bone
HP:0008090	Ankylosis of feet small joints
HP:0008093	Short 4th toe
HP:0008094	Widely spaced toes
HP:0008095	Osteolysis of talus
HP:0008096	Medially deviated second toe
HP:0008097	Partial fusion of tarsals
HP:0008102	Expanded metatarsals with widened medullary cavities
HP:0008103	Delayed tarsal ossification
HP:0008107	Plantar crease between first and second toes
HP:0008108	Advanced tarsal ossification
HP:0008110	Equinovarus deformity
HP:0008111	Broad distal hallux
HP:0008112	Plantar flexion contractures
HP:0008113	Multiple plantar creases
HP:0008114	Metatarsal diaphyseal endosteal sclerosis
HP:0008115	Clinodactyly of the 3rd toe
HP:0008116	Flexion limitation of toes
HP:0008117	Shortening of the talar neck
HP:0008119	Deformed tarsal bones
HP:0008122	Calcaneonavicular fusion
HP:0008124	Talipes calcaneovarus
HP:0008125	Second metatarsal posteriorly placed
HP:0008127	Bipartite calcaneus
HP:0008131	Tarsal stippling
HP:0008132	Medial rotation of the medial malleolus
HP:0008133	Distal tapering of metatarsals
HP:0008134	Irregular tarsal ossification
HP:0008138	Equinus calcaneus
HP:0008141	Dislocation of toes
HP:0008142	Delayed calcaneal ossification
HP:0008144	Flattening of the talar dome
HP:0008148	Impaired epinephrine-induced platelet aggregation
HP:0008150	Elevated serum transaminases during infections
HP:0008151	Prolonged prothrombin time
HP:0008153	Periodic hypokalemic paresis
HP:0008155	Mucopolysacchariduria
HP:0008158	Hyperapobetalipoproteinemia
HP:0008160	3-hydroxydicarboxylic aciduria
HP:0008161	Absent leukocyte alkaline phosphatase
HP:0008162	Asymptomatic hyperammonemia
HP:0008163	Decreased circulating cortisol level
HP:0008165	Decreased proportion circulating T-helper cells
HP:0008166	Decreased beta-galactosidase activity
HP:0008167	Very long chain fatty acid accumulation
HP:0008169	Reduced factor VII activity
HP:0008176	Neonatal unconjugated hyperbilirubinemia
HP:0008178	Abnormal cartilage matrix
HP:0008179	Decreased Arden ratio of electrooculogram
HP:0008180	Mildly elevated creatine phosphokinase
HP:0008181	Abetalipoproteinemia
HP:0008182	Adrenocortical hypoplasia
HP:0008185	Precocious puberty in males
HP:0008186	Adrenocortical cytomegaly
HP:0008187	Absence of secondary sex characteristics
HP:0008188	Thyroid dysgenesis
HP:0008189	Insulin insensitivity
HP:0008191	Thyroid agenesis
HP:0008193	Primary gonadal insufficiency
HP:0008194	Multiple pancreatic beta-cell adenomas
HP:0008197	Absence of pubertal development
HP:0008198	Congenital hypoparathyroidism
HP:0008200	Primary hyperparathyroidism
HP:0008202	Prolactin deficiency
HP:0008204	Precocious puberty with Sertoli cell tumor
HP:0008205	Insulin-dependent but ketosis-resistant diabetes
HP:0008207	Primary adrenal insufficiency
HP:0008208	Parathyroid hyperplasia
HP:0008209	Premature ovarian insufficiency
HP:0008211	Parathyroid agenesis
HP:0008213	Gonadotropin deficiency
HP:0008214	Decreased serum estradiol
HP:0008216	Adrenal gland dysgenesis
HP:0008221	Adrenal hyperplasia
HP:0008222	Female infertility
HP:0008223	Compensated hypothyroidism
HP:0008225	Thyroid follicular hyperplasia
HP:0008226	Androgen insufficiency
HP:0008227	Pituitary resistance to thyroid hormone
HP:0008229	Thyroid lymphangiectasia
HP:0008230	Decreased testosterone in males
HP:0008231	Macronodular adrenal hyperplasia
HP:0008232	Elevated circulating follicle stimulating hormone level
HP:0008233	Decreased circulating progesterone
HP:0008236	Isosexual precocious puberty
HP:0008237	Hypothalamic hypothyroidism
HP:0008239	Adrenal medullary hypoplasia
HP:0008240	Secondary growth hormone deficiency
HP:0008242	Pseudohypoaldosteronism
HP:0008244	Congenital adrenal hypoplasia
HP:0008245	Pituitary hypothyroidism
HP:0008247	Euthyroid hyperthyroxinemia
HP:0008249	Thyroid hyperplasia
HP:0008250	Infantile hypercalcemia
HP:0008251	Congenital goiter
HP:0008255	Transient neonatal diabetes mellitus
HP:0008256	Adrenocortical adenoma
HP:0008258	Congenital adrenal hyperplasia
HP:0008259	Adrenocorticotropin receptor defect
HP:0008261	Pancreatic islet cell adenoma
HP:0008263	Thyroid defect in oxidation and organification of iodide
HP:0008264	Neutrophil inclusion bodies
HP:0008265	Mitochondrial lysine transport defect
HP:0008269	Increased red cell hemolysis by shear stress
HP:0008271	Abnormal cartilage collagen
HP:0008272	Renal tubular lysine transport defect
HP:0008273	Transient aminoaciduria
HP:0008275	Abnormal light-adapted electroretinogram
HP:0008277	Abnormality of zinc homeostasis
HP:0008278	Cerebellar cortical atrophy
HP:0008279	Transient hyperlipidemia
HP:0008281	Acute hyperammonemia
HP:0008282	Unconjugated hyperbilirubinemia
HP:0008283	Fasting hyperinsulinemia
HP:0008285	Transient hypophosphatemia
HP:0008288	Nonketotic hyperglycinemia
HP:0008290	Partial complement factor H deficiency
HP:0008291	Pituitary corticotropic cell adenoma
HP:0008293	Long-chain dicarboxylic aciduria
HP:0008297	Transient hyperphenylalaninemia
HP:0008301	Dermatan sulfate excretion in urine
HP:0008303	Olivary degeneration
HP:0008305	Exercise-induced myoglobinuria
HP:0008306	Abnormal iron deposition in mitochondria
HP:0008309	Medium chain dicarboxylic aciduria
HP:0008311	Spinal cord posterior columns myelin loss
HP:0008314	Decreased activity of mitochondrial complex II
HP:0008315	Decreased plasma free carnitine
HP:0008316	Abnormal mitochondria in muscle tissue
HP:0008318	Elevated leukocyte alkaline phosphatase
HP:0008320	Impaired collagen-induced platelet aggregation
HP:0008321	Reduced factor X activity
HP:0008322	Abnormal mitochondrial morphology
HP:0008323	Abnormal light- and dark-adapted electroretinogram
HP:0008326	Vitamin B6 deficiency
HP:0008327	Microscopic nephrocalcinosis
HP:0008330	Reduced von Willebrand factor activity
HP:0008331	Elevated creatine kinase after exercise
HP:0008335	Renal aminoaciduria
HP:0008336	Complex organic aciduria
HP:0008338	Partial functional complement factor D deficiency
HP:0008339	Diaminoaciduria
HP:0008341	Distal renal tubular acidosis
HP:0008344	Elevated plasma branched chain amino acids
HP:0008345	Hypoplasia of the iris dilator muscle
HP:0008346	Increased red cell sickling tendency
HP:0008347	Decreased activity of mitochondrial complex IV
HP:0008348	Decreased circulating IgG2 level
HP:0008352	Impaired platelet adhesion
HP:0008353	Neutral hyperaminoaciduria
HP:0008354	Factor X activation deficiency
HP:0008356	obsolete Combined hyperlipidemia
HP:0008357	Reduced factor XIII activity
HP:0008358	Hyperprolinemia
HP:0008360	Neonatal hypoproteinemia
HP:0008361	Corticospinal tract pallor
HP:0008362	Aplasia/Hypoplasia of the hallux
HP:0008363	Aplasia/Hypoplasia of the tarsal bones
HP:0008364	Abnormality of the calcaneus
HP:0008365	Abnormality of the talus
HP:0008366	Contractures involving the joints of the feet
HP:0008368	Tarsal synostosis
HP:0008369	Abnormal tarsal ossification
HP:0008371	Abnormal metatarsal ossification
HP:0008372	Abnormality of vitamin A metabolism
HP:0008373	Puberty and gonadal disorders
HP:0008376	Nasal, dysarthic speech
HP:0008383	Slow-growing nails
HP:0008386	Aplasia/Hypoplasia of the nails
HP:0008388	Abnormal toenail morphology
HP:0008390	Recurrent loss of toenails and fingernails
HP:0008391	Dystrophic fingernails
HP:0008392	Subungual hyperkeratosis
HP:0008393	Congenital curved nail of fourth toe
HP:0008394	Congenital onychodystrophy
HP:0008396	Chronic monilial nail infection
HP:0008398	Hypoplastic fifth fingernail
HP:0008399	Circumungual hyperkeratosis
HP:0008400	Onycholysis of distal fingernails
HP:0008401	Onychogryposis of toenails
HP:0008402	Ridged fingernail
HP:0008404	Nail dystrophy
HP:0008407	Hyperconvex thumb nails
HP:0008410	Subungual hyperkeratotic fragments
HP:0008414	Lumbar kyphosis in infancy
HP:0008416	Six lumbar vertebrae
HP:0008417	Vertebral hypoplasia
HP:0008418	Squared-off platyspondyly
HP:0008419	Intervertebral disc degeneration
HP:0008420	Punctate vertebral calcifications
HP:0008421	Tall lumbar vertebral bodies
HP:0008422	Vertebral wedging
HP:0008423	Spinal dysplasia
HP:0008424	Hypoplastic 5th lumbar vertebrae
HP:0008425	Cuboid-shaped thoracolumbar vertebral bodies
HP:0008428	Vertebral clefting
HP:0008430	Anterior beaking of lumbar vertebrae
HP:0008432	Anterior wedging of L1
HP:0008433	Reversed usual vertebral column curves
HP:0008434	Hypoplastic cervical vertebrae
HP:0008435	Absent in utero ossification of vertebral bodies
HP:0008436	Absent/hypoplastic coccyx
HP:0008437	Bifid thoracic vertebrae
HP:0008438	Vertebral arch anomaly
HP:0008439	Lumbar hemivertebrae
HP:0008440	C1-C2 vertebral abnormality
HP:0008441	Herniation of intervertebral nuclei
HP:0008442	Vertebral hyperostosis
HP:0008443	Spinal deformities
HP:0008444	Posterior wedging of vertebral bodies
HP:0008445	Cervical spinal canal stenosis
HP:0008447	Hypoplastic coccygeal vertebrae
HP:0008449	Progressive cervical vertebral spine fusion
HP:0008450	Narrow vertebral interpedicular distance
HP:0008451	Posterior vertebral hypoplasia
HP:0008452	Wafer-thin platyspondyly
HP:0008453	Congenital kyphoscoliosis
HP:0008454	Lumbar kyphosis
HP:0008455	Dysplastic sacrum
HP:0008456	C2-C3 subluxation
HP:0008457	Caudal interpedicular narrowing
HP:0008458	Progressive congenital scoliosis
HP:0008459	Cervical vertebral agenesis
HP:0008460	Hypoplastic spinal processes
HP:0008461	Cervical vertebral facet hypoplasia
HP:0008462	Cervical instability
HP:0008463	Central vertebral hypoplasia
HP:0008464	Absent spinous processes of lower thoracic and lumbar vertebrae
HP:0008465	Absent vertebra
HP:0008467	Thoracic hemivertebrae
HP:0008468	Abnormal sacral segmentation
HP:0008469	Cervical vertebral dysplasia
HP:0008470	Lower thoracic interpediculate narrowness
HP:0008472	Prominent protruding coccyx
HP:0008473	Narrow anterio-posterior vertebral body diameter
HP:0008475	Hypoplastic sacral vertebrae
HP:0008476	Irregular sclerotic endplates
HP:0008477	Poorly ossified cervical vertebrae
HP:0008478	Scheuermann-like vertebral changes
HP:0008479	Hypoplastic vertebral bodies
HP:0008480	Cervical spondylosis
HP:0008482	Asymmetry of spinal facet joints
HP:0008483	Cervical vertebral bodies with decreased anteroposterior diameter
HP:0008484	Thoracolumbar interpediculate narrowness
HP:0008486	Lumbar interpedicular narrowing
HP:0008488	Anterior rounding of vertebral bodies
HP:0008489	Spondylolisthesis at L5-S1
HP:0008490	Sacral segmentation defect
HP:0008491	Premature anterior fontanel closure
HP:0008494	Inferior lens subluxation
HP:0008496	Multiple rows of eyelashes
HP:0008497	Congenital craniofacial dysostosis
HP:0008498	No permanent dentition
HP:0008499	High hypermetropia
HP:0008501	Median cleft lip and palate
HP:0008504	Moderate sensorineural hearing impairment
HP:0008507	Static ophthalmoparesis
HP:0008509	Aged leonine appearance
HP:0008511	Central posterior corneal opacity
HP:0008513	Bilateral conductive hearing impairment
HP:0008515	Aplasia/Hypoplasia of the vertebrae
HP:0008516	Abnormality of the vertebral spinous processes
HP:0008517	Aplasia/Hypoplasia of the sacrum
HP:0008518	Aplasia/Hypoplasia involving the vertebral column
HP:0008519	Abnormality of the coccyx
HP:0008523	Posterior helix pit
HP:0008527	Congenital sensorineural hearing impairment
HP:0008528	Long hairs growing from helix of pinna
HP:0008529	Absence of acoustic reflex
HP:0008537	Cleft at the superior portion of the pinna
HP:0008541	Superiorly displaced ears
HP:0008542	Low-frequency hearing loss
HP:0008544	Abnormally folded helix
HP:0008551	Microtia
HP:0008554	Cochlear malformation
HP:0008555	Absent vestibular function
HP:0008559	Hypoplastic superior helix
HP:0008568	Vestibular areflexia
HP:0008569	Microtia, second degree
HP:0008572	External ear malformation
HP:0008573	Low-frequency sensorineural hearing impairment
HP:0008577	Underfolded helix
HP:0008583	Underfolded superior helices
HP:0008586	Hypoplasia of the cochlea
HP:0008587	Mild neurosensory hearing impairment
HP:0008588	Slit-like opening of the exterior auditory meatus
HP:0008589	Hypoplastic helices
HP:0008591	Congenital conductive hearing impairment
HP:0008593	Prominent antitragus
HP:0008596	Postlingual sensorineural hearing impairment
HP:0008598	Mild conductive hearing impairment
HP:0008605	Unilateral external ear deformity
HP:0008606	Supraauricular pit
HP:0008607	Progressive conductive hearing impairment
HP:0008608	Hypertrophic auricular cartilage
HP:0008609	Morphological abnormality of the middle ear
HP:0008610	Infantile sensorineural hearing impairment
HP:0008615	Adult onset sensorineural hearing impairment
HP:0008619	Bilateral sensorineural hearing impairment
HP:0008625	Severe sensorineural hearing impairment
HP:0008628	Abnormality of the stapes
HP:0008629	Pulsatile tinnitus
HP:0008631	Ureteral dysgenesis
HP:0008633	Agonadism
HP:0008635	Hypertrophy of the urinary bladder
HP:0008636	Lobular glomerulopathy
HP:0008639	Gonadal hypoplasia
HP:0008640	Congenital macroorchidism
HP:0008643	Nephroblastomatosis
HP:0008647	Pubertal developmental failure in females
HP:0008648	Anteriorly displaced urethral meatus
HP:0008651	Uric acid urolithiasis independent of gout
HP:0008652	Autonomic erectile dysfunction
HP:0008653	Crescentic glomerulonephritis
HP:0008655	Aplasia/Hypoplasia of the fallopian tube
HP:0008656	Incomplete male pseudohermaphroditism
HP:0008659	Multiple small medullary renal cysts
HP:0008660	Renotubular dysgenesis
HP:0008661	Urethral stenosis
HP:0008663	Renal sarcoma
HP:0008664	Urethral sphincter sclerosis
HP:0008665	Clitoral hypertrophy
HP:0008666	Impaired histidine renal tubular absorption
HP:0008668	Gonadal dysgenesis, male
HP:0008669	Abnormal spermatogenesis
HP:0008670	Partial vaginal septum
HP:0008672	Calcium oxalate nephrolithiasis
HP:0008675	Enlarged polycystic ovaries
HP:0008676	Congenital megaureter
HP:0008677	Congenital nephrotic syndrome
HP:0008678	Renal hypoplasia/aplasia
HP:0008682	Acute tubular necrosis
HP:0008683	Enlarged labia minora
HP:0008684	Aplasia/hypoplasia of the uterus
HP:0008687	Hypoplasia of the prostate
HP:0008689	Bilateral cryptorchidism
HP:0008691	Solitary bladder diverticulum
HP:0008694	obsolete Hypertrophic labia minora
HP:0008695	Transient nephrotic syndrome
HP:0008696	Renal hamartoma
HP:0008697	Hypoplasia of the fallopian tube
HP:0008702	Absent internal genitalia
HP:0008703	Gonadal calcification
HP:0008705	Ureteral triplication
HP:0008706	Distal urethral duplication
HP:0008707	Absent scrotum
HP:0008708	Partial development of the penile shaft
HP:0008711	Benign prostatic hyperplasia
HP:0008714	Ureterovesical stenosis
HP:0008715	Testicular dysgenesis
HP:0008716	Urethrovaginal fistula
HP:0008717	Unilateral renal atrophy
HP:0008718	Unilateral renal dysplasia
HP:0008720	Primary testicular failure
HP:0008722	Urethral diverticulum
HP:0008723	Gonadal dysgenesis with female appearance, male
HP:0008724	Hypoplasia of the ovary
HP:0008726	Hypoplasia of the vagina
HP:0008729	Absence of labia majora
HP:0008730	Female external genitalia in individual with 46,XY karyotype
HP:0008732	Renal hypophosphatemia
HP:0008733	Dysplastic testes
HP:0008734	Decreased testicular size
HP:0008736	Hypoplasia of penis
HP:0008738	Partially duplicated kidney
HP:0008739	Labial pseudohypertrophy
HP:0008740	Longitudinal vaginal septum
HP:0008742	Prominent prostate median bar
HP:0008743	Coronal hypospadias
HP:0008744	Abnormality of the aryepiglottic fold
HP:0008747	Cartilaginous ossification of larynx
HP:0008749	Laryngeal hypoplasia
HP:0008750	Laryngeal atresia
HP:0008751	Laryngeal cleft
HP:0008752	Laryngeal cartilage malformation
HP:0008753	Aplasia of the epiglottis
HP:0008754	Laryngeal calcification
HP:0008755	Laryngotracheomalacia
HP:0008756	Bowing of the vocal cords
HP:0008757	Unilateral vocal cord paralysis
HP:0008760	Violent behavior
HP:0008762	Repetitive compulsive behavior
HP:0008763	No social interaction
HP:0008765	Auditory hallucinations
HP:0008767	Self-mutilation of tongue and lips due to involuntary movements
HP:0008768	Inappropriate sexual behavior
HP:0008770	Obsessive-compulsive trait
HP:0008771	Aplasia/Hypoplasia of the ear
HP:0008772	Aplasia/Hypoplasia of the external ear
HP:0008773	Aplasia/Hypoplasia of the middle ear
HP:0008774	Aplasia/Hypoplasia of the inner ear
HP:0008775	Abnormality of the prostate
HP:0008776	Abnormal renal artery morphology
HP:0008777	Abnormal vocal cord morphology
HP:0008780	Congenital bilateral hip dislocation
HP:0008783	Wide proximal femoral metaphysis
HP:0008784	Wide capital femoral epiphyses
HP:0008785	Delayed ossification of pubic rami
HP:0008786	Iliac crest serration
HP:0008788	Delayed pubic bone ossification
HP:0008789	Cone-shaped capital femoral epiphysis
HP:0008794	Dysplastic iliac wings
HP:0008796	Externally rotated hips
HP:0008797	Early ossification of capital femoral epiphyses
HP:0008798	Widened sacrosciatic notch
HP:0008800	Limited hip movement
HP:0008801	Hypoplasia of the lesser trochanter
HP:0008802	Hypoplasia of the femoral head
HP:0008803	Narrow sacroiliac notch
HP:0008804	Broad femoral head
HP:0008807	Acetabular dysplasia
HP:0008808	High iliac wings
HP:0008812	Flattened femoral head
HP:0008817	Aplastic pubic bones
HP:0008818	Large iliac wings
HP:0008819	Narrow femoral neck
HP:0008820	Absent ossification of capital femoral epiphysis
HP:0008821	Hypoplastic inferior ilia
HP:0008822	Hypoplastic ischiopubic rami
HP:0008823	Hypoplastic inferior pubic rami
HP:0008824	Hypoplastic iliac body
HP:0008826	Dislocation of the femoral head
HP:0008828	Delayed proximal femoral epiphyseal ossification
HP:0008829	Delayed femoral head ossification
HP:0008830	Hypoplastic pubic rami
HP:0008833	Irregular acetabular roof
HP:0008835	Multicentric femoral head ossification
HP:0008838	Stippled calcification proximal humeral epiphyses
HP:0008839	Hypoplastic pelvis
HP:0008843	Hip osteoarthritis
HP:0008845	Mesomelic short stature
HP:0008846	Severe intrauterine growth retardation
HP:0008848	Moderately short stature
HP:0008850	Severe postnatal growth retardation
HP:0008855	Moderate postnatal growth retardation
HP:0008857	Neonatal short-trunk short stature
HP:0008866	Failure to thrive secondary to recurrent infections
HP:0008872	Feeding difficulties in infancy
HP:0008873	Disproportionate short-limb short stature
HP:0008883	Mild intrauterine growth retardation
HP:0008887	Adipose tissue loss
HP:0008890	Severe short-limb dwarfism
HP:0008897	Postnatal growth retardation
HP:0008905	Rhizomelia
HP:0008909	Lethal short-limbed short stature
HP:0008915	Childhood-onset truncal obesity
HP:0008921	Neonatal short-limb short stature
HP:0008922	Childhood-onset short-trunk short stature
HP:0008929	Asymmetric short stature
HP:0008935	Generalized neonatal hypotonia
HP:0008936	Muscular hypotonia of the trunk
HP:0008940	Generalized lymphadenopathy
HP:0008942	Acute rhabdomyolysis
HP:0008944	Distal lower limb amyotrophy
HP:0008945	Loss of ability to walk in early childhood
HP:0008946	Pelvic girdle amyotrophy
HP:0008947	Infantile muscular hypotonia
HP:0008948	Proximal upper limb amyotrophy
HP:0008952	Shoulder muscle hypoplasia
HP:0008953	Pectoralis major hypoplasia
HP:0008954	Intrinsic hand muscle atrophy
HP:0008955	Progressive distal muscular atrophy
HP:0008956	Proximal lower limb amyotrophy
HP:0008959	Distal upper limb muscle weakness
HP:0008962	Calf muscle hypoplasia
HP:0008963	Tibialis muscle weakness
HP:0008964	Nonprogressive muscular atrophy
HP:0008967	Exercise-induced muscle stiffness
HP:0008968	Muscle hypertrophy of the lower extremities
HP:0008969	Leg muscle stiffness
HP:0008970	Scapulohumeral muscular dystrophy
HP:0008972	Decreased activity of mitochondrial respiratory chain
HP:0008978	Necrotizing myopathy
HP:0008981	Calf muscle hypertrophy
HP:0008984	Neck muscle hypoplasia
HP:0008985	Increased intramuscular fat
HP:0008986	Agenesis of the diaphragm
HP:0008988	Pelvic girdle muscle atrophy
HP:0008991	Exercise-induced leg cramps
HP:0008993	Increased intraabdominal fat
HP:0008994	Proximal muscle weakness in lower limbs
HP:0008997	Proximal muscle weakness in upper limbs
HP:0008998	Pectoralis hypoplasia
HP:0009002	Loss of truncal subcutaneous adipose tissue
HP:0009003	Increased subcutaneous truncal adipose tissue
HP:0009004	Hypoplasia of the musculature
HP:0009005	Weakness of the intrinsic hand muscles
HP:0009007	Biceps hypoplasia
HP:0009011	Hypoplasia of serratus anterior muscle
HP:0009013	Congenital absence of gluteal muscles
HP:0009016	Upper limb muscle hypoplasia
HP:0009017	Loss of gluteal subcutaneous adipose tissue
HP:0009019	Progressive loss of facial adipose tissue
HP:0009020	Exercise-induced muscle fatigue
HP:0009023	Abdominal wall muscle weakness
HP:0009025	Increased connective tissue
HP:0009026	Hypoplasia of latissimus dorsi muscle
HP:0009027	Foot dorsiflexor weakness
HP:0009028	Generalized weakness of limb muscles
HP:0009031	Amyotrophy of ankle musculature
HP:0009037	Segmental spinal muscular atrophy
HP:0009042	Marked muscular hypertrophy
HP:0009044	obsolete Hypoplasia of deltoid muscle
HP:0009045	Exercise-induced rhabdomyolysis
HP:0009046	Difficulty running
HP:0009049	Peroneal muscle atrophy
HP:0009050	Quadriceps muscle atrophy
HP:0009051	Increased muscle glycogen content
HP:0009053	Distal lower limb muscle weakness
HP:0009054	Scapuloperoneal myopathy
HP:0009055	Generalized limb muscle atrophy
HP:0009056	Loss of subcutaneous adipose tissue from upper limbs
HP:0009058	Increased muscle lipid content
HP:0009059	Congenital generalized lipodystrophy
HP:0009060	Scapular muscle atrophy
HP:0009062	Infantile axial hypotonia
HP:0009063	Progressive distal muscle weakness
HP:0009064	Generalized lipodystrophy
HP:0009067	Progressive spinal muscular atrophy
HP:0009069	Lethal infantile mitochondrial myopathy
HP:0009071	Inflammatory myopathy
HP:0009072	Decreased Achilles reflex
HP:0009073	Progressive proximal muscle weakness
HP:0009077	Weakness of long finger extensor muscles
HP:0009084	Midline notch of upper alveolar ridge
HP:0009085	Alveolar ridge overgrowth
HP:0009087	Posteriorly placed tongue
HP:0009088	Speech articulation difficulties
HP:0009090	obsolete Facial diplegic appearance
HP:0009092	Progressive alveolar ridge hypertropy
HP:0009094	Cleft lower alveolar ridge
HP:0009098	Chronic oral candidiasis
HP:0009099	Median cleft palate
HP:0009100	Thick anterior alveolar ridges
HP:0009101	Submucous cleft lip
HP:0009102	Anterior open-bite malocclusion
HP:0009103	Aplasia/Hypoplasia involving the pelvis
HP:0009104	Aplasia/Hypoplasia of the pubic bone
HP:0009105	Abnormal ossification of the pubic bone
HP:0009106	Abnormal pelvis bone ossification
HP:0009107	Abnormal ossification involving the femoral head and neck
HP:0009108	Aplasia/Hypoplasia involving the femoral head and neck
HP:0009109	Denervation of the diaphragm
HP:0009110	Diaphragmatic eventration
HP:0009112	Absent left hemidiaphragm
HP:0009113	Diaphragmatic weakness
HP:0009115	Aplasia/hypoplasia involving the skeleton
HP:0009116	Aplasia/Hypoplasia involving bones of the skull
HP:0009117	Aplasia/Hypoplasia of the maxilla
HP:0009118	Aplasia/Hypoplasia of the mandible
HP:0009119	Aplasia/Hypoplasia of the frontal sinuses
HP:0009120	Aplasia/Hypoplasia involving the sinuses
HP:0009121	Abnormal axial skeleton morphology
HP:0009122	Aplasia/hypoplasia affecting bones of the axial skeleton
HP:0009123	Mixed hypo- and hyperpigmentation of the skin
HP:0009124	Abnormal adipose tissue morphology
HP:0009125	Lipodystrophy
HP:0009126	Increased adipose tissue
HP:0009127	Abnormality of the musculature of the limbs
HP:0009128	Aplasia/Hypoplasia involving the musculature of the extremities
HP:0009129	Upper limb amyotrophy
HP:0009130	Hand muscle atrophy
HP:0009131	Abnormality of the musculature of the thorax
HP:0009132	Abnormal tarsal bone mineral density
HP:0009134	Osteolysis involving bones of the feet
HP:0009136	Duplication involving bones of the feet
HP:0009138	Synostosis involving bones of the lower limbs
HP:0009139	Osteolysis involving bones of the lower limbs
HP:0009140	Synostosis involving bones of the feet
HP:0009141	Depletion of mitochondrial DNA in muscle tissue
HP:0009142	Duplication of bones involving the upper extremities
HP:0009144	Supernumerary bones of the axial skeleton
HP:0009145	Abnormal cerebral artery morphology
HP:0009147	Enlarged epiphysis of the distal phalanx of the 5th finger
HP:0009148	Small epiphysis of the distal phalanx of the 5th finger
HP:0009149	Triangular epiphysis of the distal phalanx of the 5th finger
HP:0009150	Abnormality of the proximal phalanx of the 5th finger
HP:0009152	Abnormality of the epiphyses of the 5th finger
HP:0009153	Abnormality of the epiphysis of the proximal phalanx of the 5th finger
HP:0009154	Triangular epiphysis of the proximal phalanx of the 5th finger
HP:0009155	Cone-shaped epiphysis of the proximal phalanx of the 5th finger
HP:0009157	Ivory epiphysis of the proximal phalanx of the 5th finger
HP:0009158	Enlarged epiphysis of the proximal phalanx of the 5th finger
HP:0009159	Small epiphysis of the proximal phalanx of the 5th finger
HP:0009160	Absent epiphysis of the proximal phalanx of the 5th finger
HP:0009161	Aplasia/Hypoplasia of the middle phalanx of the 5th finger
HP:0009162	Absent middle phalanx of 5th finger
HP:0009163	obsolete Abnormal form of the 5th finger
HP:0009164	Abnormal calcification of the carpal bones
HP:0009165	Stippling of the epiphysis of the distal phalanx of the 5th finger
HP:0009166	Fragmentation of the epiphysis of the distal phalanx of the 5th finger
HP:0009167	Irregular epiphysis of the distal phalanx of the 5th finger
HP:0009168	Bullet-shaped middle phalanx of the 5th finger
HP:0009169	Broad middle phalanx of the 5th finger
HP:0009170	Osteolytic defects of the middle phalanx of the 5th finger
HP:0009171	Triangular epiphyses of the metacarpals
HP:0009172	Abnormal 4th finger phalanx morphology
HP:0009173	Curved middle phalanx of the 5th finger
HP:0009174	Abnormality of the epiphyses of the 4th finger
HP:0009175	Patchy sclerosis of the middle phalanx of the 5th finger
HP:0009177	Proximal/middle symphalangism of 5th finger
HP:0009178	Symphalangism of middle phalanx of 5th finger
HP:0009179	Deviation of the 5th finger
HP:0009180	Ulnar deviation of the 5th finger
HP:0009182	Triangular shaped middle phalanx of the 5th finger
HP:0009183	Joint contracture of the 5th finger
HP:0009184	Contracture of the distal interphalangeal joint of the 5th finger
HP:0009185	Contracture of the proximal interphalangeal joint of the 5th finger
HP:0009186	Contracture of the metacarpophalangeal joint of the 5th finger
HP:0009187	Bracket epiphysis of the distal phalanx of the 5th finger
HP:0009188	Pseudoepiphysis of the distal phalanx of the 5th finger
HP:0009189	Fragmentation of the metacarpal epiphyses
HP:0009190	Irregular epiphyses of the metacarpals
HP:0009191	Ivory epiphyses of the metacarpals
HP:0009192	Aplasia/Hypoplasia of the proximal phalanx of the 5th finger
HP:0009193	Pseudoepiphyses of the metacarpals
HP:0009194	Small epiphyses of the metacarpals
HP:0009195	Epiphyseal stippling of the metacarpals
HP:0009196	Absent metacarpal epiphyses
HP:0009197	Bracket epiphysis of the proximal phalanx of the 5th finger
HP:0009198	Abnormality of the epiphysis of the distal phalanx of the 5th finger
HP:0009199	Irregular epiphysis of the proximal phalanx of the 5th finger
HP:0009200	Pseudoepiphysis of the proximal phalanx of the 5th finger
HP:0009201	Stippling of the epiphysis of the proximal phalanx of the 5th finger
HP:0009202	Fragmentation of the epiphysis of the proximal phalanx of the 5th finger
HP:0009203	Absent epiphysis of the middle phalanx of the 5th finger
HP:0009204	Bracket epiphysis of the middle phalanx of the 5th finger
HP:0009205	Cone-shaped epiphysis of the middle phalanx of the 5th finger
HP:0009206	Enlarged epiphysis of the middle phalanx of the 5th finger
HP:0009207	Fragmentation of the epiphysis of the middle phalanx of the 5th finger
HP:0009208	Irregular epiphysis of the middle phalanx of the 5th finger
HP:0009209	Ivory epiphysis of the middle phalanx of the 5th finger
HP:0009210	Pseudoepiphysis of the middle phalanx of the 5th finger
HP:0009211	Small epiphysis of the middle phalanx of the 5th finger
HP:0009212	Stippling of the epiphysis of the middle phalanx of the 5th finger
HP:0009213	Triangular epiphysis of the middle phalanx of the 5th finger
HP:0009214	Absent epiphysis of the middle phalanx of the 4th finger
HP:0009215	Bracket epiphysis of the middle phalanx of the 4th finger
HP:0009216	Cone-shaped epiphysis of the middle phalanx of the 4th finger
HP:0009217	Enlarged epiphysis of the middle phalanx of the 4th finger
HP:0009218	Fragmentation of the epiphysis of the middle phalanx of the 4th finger
HP:0009219	Irregular epiphysis of the middle phalanx of the 4th finger
HP:0009220	Ivory epiphysis of the middle phalanx of the 4th finger
HP:0009221	Pseudoepiphysis of the middle phalanx of the 4th finger
HP:0009222	Small epiphysis of the middle phalanx of the 4th finger
HP:0009223	Stippling of the epiphysis of the middle phalanx of the 4th finger
HP:0009224	Triangular epiphysis of the middle phalanx of the 4th finger
HP:0009225	Aplasia of the proximal phalanx of the 5th finger
HP:0009226	Short proximal phalanx of the 5th finger
HP:0009227	Broad proximal phalanx of the 5th finger
HP:0009228	Bullet-shaped proximal phalanx of the 5th finger
HP:0009229	Curved proximal phalanx of the 5th finger
HP:0009230	Osteolytic defects of the proximal phalanx of the 5th finger
HP:0009231	Patchy sclerosis of the proximal phalanx of the 5th finger
HP:0009232	Symphalangism affecting the proximal phalanx of the 5th finger
HP:0009233	Triangular shaped proximal phalanx of the 5th finger
HP:0009234	Symphalangism of the proximal phalanx of the 5th finger with the 5th metacarpal
HP:0009236	Rhomboid or triangular shaped 5th finger proximal phalanx
HP:0009237	Short 5th finger
HP:0009238	Aplasia of the 5th finger
HP:0009239	Aplasia/Hypoplasia of the distal phalanx of the 5th finger
HP:0009240	Broad distal phalanx of the 5th finger
HP:0009241	Bullet-shaped distal phalanx of the 5th finger
HP:0009242	Osteolytic defects of the distal phalanx of the 5th finger
HP:0009243	Patchy sclerosis of the distal phalanx of the 5th finger
HP:0009244	Distal/middle symphalangism of 5th finger
HP:0009245	Triangular shaped distal phalanx of the 5th finger
HP:0009246	Aplasia of the distal phalanx of the 5th finger
HP:0009247	Abnormality of the epiphysis of the middle phalanx of the 4th finger
HP:0009248	Abnormality of the epiphysis of the proximal phalanx of the 4th finger
HP:0009249	Abnormality of the epiphysis of the distal phalanx of the 4th finger
HP:0009250	Absent epiphysis of the distal phalanx of the 4th finger
HP:0009251	Bracket epiphysis of the distal phalanx of the 4th finger
HP:0009252	Cone-shaped epiphysis of the distal phalanx of the 4th finger
HP:0009253	Enlarged epiphysis of the distal phalanx of the 4th finger
HP:0009254	Fragmentation of the epiphysis of the distal phalanx of the 4th finger
HP:0009255	Irregular epiphysis of the distal phalanx of the 4th finger
HP:0009256	Ivory epiphysis of the distal phalanx of the 4th finger
HP:0009257	Pseudoepiphysis of the distal phalanx of the 4th finger
HP:0009258	Small epiphysis of the distal phalanx of the 4th finger
HP:0009259	Stippling of the epiphysis of the distal phalanx of the 4th finger
HP:0009260	Triangular epiphysis of the distal phalanx of the 4th finger
HP:0009261	Absent epiphysis of the proximal phalanx of the 4th finger
HP:0009262	Bracket epiphysis of the proximal phalanx of the 4th finger
HP:0009263	Cone-shaped epiphysis of the proximal phalanx of the 4th finger
HP:0009264	Enlarged epiphysis of the proximal phalanx of the 4th finger
HP:0009265	Fragmentation of the epiphysis of the proximal phalanx of the 4th finger
HP:0009266	Irregular epiphysis of the proximal phalanx of the 4th finger
HP:0009267	Ivory epiphysis of the proximal phalanx of the 4th finger
HP:0009268	Pseudoepiphysis of the proximal phalanx of the 4th finger
HP:0009269	Small epiphysis of the proximal phalanx of the 4th finger
HP:0009270	Stippling of the epiphysis of the proximal phalanx of the 4th finger
HP:0009271	Triangular epiphysis of the proximal phalanx of the 4th finger
HP:0009272	Aplasia/Hypoplasia of the 4th finger
HP:0009273	Deviation of the 4th finger
HP:0009274	Joint contracture of the 4th finger
HP:0009275	Contracture of the distal interphalangeal joint of the 4th finger
HP:0009276	Contracture of the proximal interphalangeal joint of the 4th finger
HP:0009277	Contracture of the metacarpophalangeal joint of the 4th finger
HP:0009278	Ulnar deviation of the 4th finger
HP:0009279	Radial deviation of the 4th finger
HP:0009280	Short 4th finger
HP:0009281	Aplasia of the 4th finger
HP:0009282	Abnormality of the distal phalanx of the 4th finger
HP:0009283	Abnormality of the middle phalanx of the 4th finger
HP:0009284	Abnormality of the proximal phalanx of the 4th finger
HP:0009285	Curved phalanges of the 4th finger
HP:0009286	Curved distal phalanx of the 4th finger
HP:0009287	Curved middle phalanx of the 4th finger
HP:0009288	Curved proximal phalanx of the 4th finger
HP:0009289	Aplasia/Hypoplasia of the distal phalanx of the 4th finger
HP:0009290	Short distal phalanx of the 4th finger
HP:0009291	Aplasia of the distal phalanx of the 4th finger
HP:0009292	Broad distal phalanx of the 4th finger
HP:0009293	Broad middle phalanx of the 4th finger
HP:0009294	Absent middle phalanx of 4th finger
HP:0009295	Short middle phalanx of the 4th finger
HP:0009296	Bullet-shaped middle phalanx of the 4th finger
HP:0009297	Osteolytic defects of the middle phalanx of the 4th finger
HP:0009298	Aplasia of the proximal phalanx of the 4th finger
HP:0009299	Aplasia/Hypoplasia of the middle phalanx of the 4th finger
HP:0009300	Aplasia/Hypoplasia of the proximal phalanx of the 4th finger
HP:0009301	Short proximal phalanx of the 4th finger
HP:0009302	Bullet-shaped distal phalanx of the 4th finger
HP:0009303	Osteolytic defects of the distal phalanx of the 4th finger
HP:0009304	Patchy sclerosis of the distal phalanx of the 4th finger
HP:0009305	Distal/middle symphalangism of 4th finger
HP:0009306	Triangular shaped distal phalanx of the 4th finger
HP:0009307	Patchy sclerosis of the middle phalanx of the 4th finger
HP:0009308	Symphalangism of middle phalanx of 4th finger
HP:0009309	Triangular shaped middle phalanx of the 4th finger
HP:0009310	Broad proximal phalanx of the 4th finger
HP:0009311	Bullet-shaped proximal phalanx of the 4th finger
HP:0009312	Osteolytic defects of the proximal phalanx of the 4th finger
HP:0009313	Patchy sclerosis of the proximal phalanx of the 4th finger
HP:0009314	Symphalangism affecting the proximal phalanx of the 4th finger
HP:0009315	Triangular shaped proximal phalanx of the 4th finger
HP:0009316	Abnormal 3rd finger phalanx morphology
HP:0009317	Deviation of the 3rd finger
HP:0009318	Aplasia/Hypoplasia of the 3rd finger
HP:0009319	Joint contracture of the 3rd finger
HP:0009320	Abnormality of the epiphyses of the 3rd finger
HP:0009321	Absent epiphysis of the middle phalanx of the 3rd finger
HP:0009322	Bracket epiphysis of the middle phalanx of the 3rd finger
HP:0009323	Cone-shaped epiphysis of the middle phalanx of the 3rd finger
HP:0009324	Enlarged epiphysis of the middle phalanx of the 3rd finger
HP:0009325	Fragmentation of the epiphysis of the middle phalanx of the 3rd finger
HP:0009326	Irregular epiphysis of the middle phalanx of the 3rd finger
HP:0009327	Ivory epiphysis of the middle phalanx of the 3rd finger
HP:0009328	Pseudoepiphysis of the middle phalanx of the 3rd finger
HP:0009329	Small epiphysis of the middle phalanx of the 3rd finger
HP:0009330	Stippling of the epiphysis of the middle phalanx of the 3rd finger
HP:0009331	Triangular epiphysis of the middle phalanx of the 3rd finger
HP:0009332	Abnormality of the epiphysis of the distal phalanx of the 3rd finger
HP:0009333	Abnormality of the epiphysis of the proximal phalanx of the 3rd finger
HP:0009334	Abnormality of the epiphysis of the middle phalanx of the 3rd finger
HP:0009335	Absent epiphysis of the distal phalanx of the 3rd finger
HP:0009336	Bracket epiphysis of the distal phalanx of the 3rd finger
HP:0009337	Cone-shaped epiphysis of the distal phalanx of the 3rd finger
HP:0009338	Enlarged epiphysis of the distal phalanx of the 3rd finger
HP:0009339	Fragmentation of the epiphysis of the distal phalanx of the 3rd finger
HP:0009340	Irregular epiphysis of the distal phalanx of the 3rd finger
HP:0009341	Ivory epiphysis of the distal phalanx of the 3rd finger
HP:0009342	Pseudoepiphysis of the distal phalanx of the 3rd finger
HP:0009343	Small epiphysis of the distal phalanx of the 3rd finger
HP:0009344	Stippling of the epiphysis of the distal phalanx of the 3rd finger
HP:0009345	Triangular epiphysis of the distal phalanx of the 3rd finger
HP:0009346	Absent epiphysis of the proximal phalanx of the 3rd finger
HP:0009347	Bracket epiphysis of the proximal phalanx of the 3rd finger
HP:0009348	Cone-shaped epiphysis of the proximal phalanx of the 3rd finger
HP:0009349	Enlarged epiphysis of the proximal phalanx of the 3rd finger
HP:0009350	Fragmentation of the epiphysis of the proximal phalanx of the 3rd finger
HP:0009351	Irregular epiphysis of the proximal phalanx of the 3rd finger
HP:0009352	Ivory epiphysis of the proximal phalanx of the 3rd finger
HP:0009353	Pseudoepiphysis of the proximal phalanx of the 3rd finger
HP:0009354	Small epiphysis of the proximal phalanx of the 3rd finger
HP:0009355	Stippling of the epiphysis of the proximal phalanx of the 3rd finger
HP:0009356	Triangular epiphysis of the proximal phalanx of the 3rd finger
HP:0009357	Abnormality of the distal phalanx of the 3rd finger
HP:0009358	Abnormality of the proximal phalanx of the 3rd finger
HP:0009370	Type A brachydactyly
HP:0009371	Type A1 brachydactyly
HP:0009372	Type A2 brachydactyly
HP:0009373	Type C brachydactyly
HP:0009374	Broad phalanges of the 5th finger
HP:0009375	Bullet-shaped phalanges of the 5th finger
HP:0009376	Aplasia/Hypoplasia of the phalanges of the 5th finger
HP:0009377	Patchy sclerosis of 5th finger phalanx
HP:0009378	Triangular shaped phalanges of the 5th finger
HP:0009379	Rhomboid or triangular shaped 5th finger distal phalanx
HP:0009380	Aplasia of the fingers
HP:0009381	Short finger
HP:0009382	Absent epiphyses of the 5th finger
HP:0009383	Bracket epiphyses of the 5th finger
HP:0009384	Cone-shaped epiphyses of the 5th finger
HP:0009385	Enlarged epiphyses of the 5th finger
HP:0009386	Fragmentation of the epiphyses of the 5th finger
HP:0009387	Irregular epiphyses of the 5th finger
HP:0009388	Ivory epiphyses of the 5th finger
HP:0009389	Pseudoepiphyses of the 5th finger
HP:0009390	Small epiphyses of the 5th finger
HP:0009391	Stippling of the epiphyses of the 5th finger
HP:0009392	Triangular epiphyses of the 5th finger
HP:0009393	Absent epiphyses of the 4th finger
HP:0009394	Bracket epiphyses of the 4th finger
HP:0009395	Cone-shaped epiphyses of the 4th finger
HP:0009396	Enlarged epiphyses of the 4th finger
HP:0009397	Fragmentation of the epiphyses of the 4th finger
HP:0009398	Irregular epiphyses of the 4th finger
HP:0009399	Ivory epiphyses of the 4th finger
HP:0009400	Pseudoepiphyses of the 4th finger
HP:0009401	Small epiphyses of the 4th finger
HP:0009402	Stippling of the epiphyses of the 4th finger
HP:0009403	Triangular epiphyses of the 4th finger
HP:0009404	Broad phalanges of the 4th finger
HP:0009405	Bullet-shaped phalanges of the 4th finger
HP:0009406	Patchy sclerosis of 4th finger phalanx
HP:0009407	Triangular shaped phalanges of the 4th finger
HP:0009408	Aplasia/Hypoplasia of the phalanges of the 4th finger
HP:0009410	Absent epiphyses of the 3rd finger
HP:0009411	Bracket epiphyses of the 3rd finger
HP:0009412	Cone-shaped epiphyses of the 3rd finger
HP:0009413	Enlarged epiphyses of the 3rd finger
HP:0009414	Fragmentation of the epiphyses of the 3rd finger
HP:0009415	Irregular epiphyses of the 3rd finger
HP:0009416	Ivory epiphyses of the 3rd finger
HP:0009417	Pseudoepiphyses of the 3rd finger
HP:0009418	Small epiphyses of the 3rd finger
HP:0009419	Stippling of the epiphyses of the 3rd finger
HP:0009420	Triangular epiphyses of the 3rd finger
HP:0009421	Aplasia/Hypoplasia of the distal phalanx of the 3rd finger
HP:0009422	Broad distal phalanx of the 3rd finger
HP:0009423	Bullet-shaped distal phalanx of the 3rd finger
HP:0009424	Osteolytic defects of the distal phalanx of the 3rd finger
HP:0009425	Patchy sclerosis of the distal phalanx of the 3rd finger
HP:0009426	Distal/middle symphalangism of 3rd finger
HP:0009427	Triangular shaped distal phalanx of the 3rd finger
HP:0009428	Curved distal phalanx of the 3rd finger
HP:0009429	Aplasia of the distal phalanx of the 3rd finger
HP:0009430	Broad middle phalanx of the 3rd finger
HP:0009431	Bullet-shaped middle phalanx of the 3rd finger
HP:0009432	Curved middle phalanx of the 3rd finger
HP:0009433	Osteolytic defects of the middle phalanx of the 3rd finger
HP:0009434	Patchy sclerosis of the middle phalanx of the 3rd finger
HP:0009435	Symphalangism of middle phalanx of 3rd finger
HP:0009436	Triangular shaped middle phalanx of the 3rd finger
HP:0009437	Aplasia/Hypoplasia of the middle phalanx of the 3rd finger
HP:0009438	Absent middle phalanx of 3rd finger
HP:0009439	Short middle phalanx of the 3rd finger
HP:0009440	Broad phalanges of the 3rd finger
HP:0009441	Bullet-shaped phalanges of the 3rd finger
HP:0009442	Curved phalanges of the 3rd finger
HP:0009443	Osteolytic defects of the phalanges of the 3rd finger
HP:0009444	Patchy sclerosis of 3rd finger phalanx
HP:0009445	Symphalangism of the 3rd finger
HP:0009446	Triangular shaped phalanges of the 3rd finger
HP:0009447	Aplasia/Hypoplasia of the phalanges of the 3rd finger
HP:0009448	obsolete Aplasia of the phalanges of the 3rd finger
HP:0009449	obsolete Hypoplastic/small phalanges of the 3rd finger
HP:0009450	Broad proximal phalanx of the 3rd finger
HP:0009451	Bullet-shaped proximal phalanx of the 3rd finger
HP:0009452	Curved proximal phalanx of the 3rd finger
HP:0009453	Osteolytic defects of the proximal phalanx of the 3rd finger
HP:0009454	Patchy sclerosis of the proximal phalanx of the 3rd finger
HP:0009455	Symphalangism affecting the proximal phalanx of the 3rd finger
HP:0009456	Triangular shaped proximal phalanx of the 3rd finger
HP:0009457	Aplasia/Hypoplasia of the proximal phalanx of the 3rd finger
HP:0009458	Aplasia of the proximal phalanx of the 3rd finger
HP:0009459	Short proximal phalanx of the 3rd finger
HP:0009460	Aplasia of the 3rd finger
HP:0009461	Short 3rd finger
HP:0009462	Radial deviation of the 3rd finger
HP:0009463	Ulnar deviation of the 3rd finger
HP:0009464	Ulnar deviation of the 2nd finger
HP:0009465	Ulnar deviation of finger
HP:0009466	Radial deviation of finger
HP:0009467	Radial deviation of the 2nd finger
HP:0009468	Deviation of the 2nd finger
HP:0009469	Contracture of the distal interphalangeal joint of the 3rd finger
HP:0009470	Contracture of the metacarpophalangeal joint of the 3rd finger
HP:0009471	Contracture of the proximal interphalangeal joint of the 3rd finger
HP:0009473	Joint contracture of the hand
HP:0009477	Proximal/middle symphalangism of 4th finger
HP:0009478	Symphalangism of the proximal phalanx of the 4th finger with the 4th metacarpal
HP:0009482	Proximal/middle symphalangism of 3rd finger
HP:0009483	Symphalangism of the proximal phalanx of the 3rd finger with the 3rd metacarpal
HP:0009484	Deviation of the hand or of fingers of the hand
HP:0009485	Radial deviation of the hand or of fingers of the hand
HP:0009486	Radial deviation of the hand
HP:0009487	Ulnar deviation of the hand
HP:0009488	Absent epiphyses of the 2nd finger
HP:0009489	Bracket epiphyses of the 2nd finger
HP:0009490	Cone-shaped epiphyses of the 2nd finger
HP:0009491	Enlarged epiphyses of the 2nd finger
HP:0009492	Fragmentation of the epiphyses of the 2nd finger
HP:0009493	Irregular epiphyses of the 2nd finger
HP:0009494	Ivory epiphyses of the 2nd finger
HP:0009495	Pseudoepiphyses of the 2nd finger
HP:0009496	Small epiphyses of the 2nd finger
HP:0009497	Stippling of the epiphyses of the 2nd finger
HP:0009498	Triangular epiphyses of the 2nd finger
HP:0009499	Abnormality of the epiphysis of the distal phalanx of the 2nd finger
HP:0009500	Abnormality of the epiphysis of the middle phalanx of the 2nd finger
HP:0009501	Abnormality of the epiphysis of the proximal phalanx of the 2nd finger
HP:0009502	Absent epiphysis of the distal phalanx of the 2nd finger
HP:0009503	Bracket epiphysis of the distal phalanx of the 2nd finger
HP:0009504	Cone-shaped epiphysis of the distal phalanx of the 2nd finger
HP:0009505	Enlarged epiphysis of the distal phalanx of the 2nd finger
HP:0009506	Fragmentation of the epiphysis of the distal phalanx of the 2nd finger
HP:0009507	Irregular epiphysis of the distal phalanx of the 2nd finger
HP:0009508	Ivory epiphysis of the distal phalanx of the 2nd finger
HP:0009509	Pseudoepiphysis of the distal phalanx of the 2nd finger
HP:0009510	Small epiphysis of the distal phalanx of the 2nd finger
HP:0009511	Stippling of the epiphysis of the distal phalanx of the 2nd finger
HP:0009512	Triangular epiphysis of the distal phalanx of the 2nd finger
HP:0009513	Absent epiphysis of the middle phalanx of the 2nd finger
HP:0009514	Bracket epiphysis of the middle phalanx of the 2nd finger
HP:0009515	Cone-shaped epiphysis of the middle phalanx of the 2nd finger
HP:0009516	Enlarged epiphysis of the middle phalanx of the 2nd finger
HP:0009517	Fragmentation of the epiphysis of the middle phalanx of the 2nd finger
HP:0009518	Irregular epiphysis of the middle phalanx of the 2nd finger
HP:0009519	Ivory epiphysis of the middle phalanx of the 2nd finger
HP:0009520	Pseudoepiphysis of the middle phalanx of the 2nd finger
HP:0009521	Small epiphysis of the middle phalanx of the 2nd finger
HP:0009522	Stippling of the epiphysis of the middle phalanx of the 2nd finger
HP:0009523	Triangular epiphysis of the middle phalanx of the 2nd finger
HP:0009524	Absent epiphysis of the proximal phalanx of the 2nd finger
HP:0009525	Bracket epiphysis of the proximal phalanx of the 2nd finger
HP:0009526	Cone-shaped epiphysis of the proximal phalanx of the 2nd finger
HP:0009527	Enlarged epiphysis of the proximal phalanx of the 2nd finger
HP:0009528	Fragmentation of the epiphysis of the proximal phalanx of the 2nd finger
HP:0009529	Irregular epiphysis of the proximal phalanx of the 2nd finger
HP:0009530	Ivory epiphysis of the proximal phalanx of the 2nd finger
HP:0009531	Pseudoepiphysis of the proximal phalanx of the 2nd finger
HP:0009532	Small epiphysis of the proximal phalanx of the 2nd finger
HP:0009533	Stippling of the epiphysis of the proximal phalanx of the 2nd finger
HP:0009534	Triangular epiphysis of the proximal phalanx of the 2nd finger
HP:0009535	Aplasia of the 2nd finger
HP:0009536	Short 2nd finger
HP:0009537	Flexion contracture of the 2nd finger
HP:0009538	Contracture of the distal interphalangeal joint of the 2nd finger
HP:0009539	Contracture of the metacarpophalangeal joint of the 2nd finger
HP:0009540	Contracture of the proximal interphalangeal joint of the 2nd finger
HP:0009541	Abnormality of the phalanges of the 2nd finger
HP:0009542	Abnormality of the distal phalanx of the 2nd finger
HP:0009543	Abnormality of the middle phalanx of the 2nd finger
HP:0009544	Abnormality of the proximal phalanx of the 2nd finger
HP:0009545	Symphalangism of the 2nd finger
HP:0009546	Triangular shaped phalanges of the 2nd finger
HP:0009547	Broad phalanges of the 2nd finger
HP:0009548	Bullet-shaped phalanges of the 2nd finger
HP:0009549	Curved phalanges of the 2nd finger
HP:0009550	Osteolytic defects of the phalanges of the 2nd finger
HP:0009551	Patchy sclerosis of 2nd finger phalanx
HP:0009552	Aplasia/Hypoplasia of the phalanges of the 2nd finger
HP:0009553	Abnormality of the hairline
HP:0009554	Projection of scalp hair onto lateral cheek
HP:0009555	Hypoplasia of the pharynx
HP:0009556	Absent tibia
HP:0009557	Aplasia/Hypoplasia of the distal phalanx of the 2nd finger
HP:0009558	Broad distal phalanx of the 2nd finger
HP:0009559	Bullet-shaped distal phalanx of the 2nd finger
HP:0009560	Curved distal phalanx of the 2nd finger
HP:0009561	Osteolytic defects of the distal phalanx of the 2nd finger
HP:0009562	Patchy sclerosis of the distal phalanx of the 2nd finger
HP:0009563	Distal/middle symphalangism of 2nd finger
HP:0009564	Triangular shaped distal phalanx of the 2nd finger
HP:0009565	Aplasia of the distal phalanx of the 2nd finger
HP:0009566	Short distal phalanx of the 2nd finger
HP:0009568	Aplasia/Hypoplasia of the middle phalanx of the 2nd finger
HP:0009569	Broad middle phalanx of the 2nd finger
HP:0009570	Bullet-shaped middle phalanx of the 2nd finger
HP:0009571	Curved middle phalanx of the 2nd finger
HP:0009572	Osteolytic defects of the middle phalanx of the 2nd finger
HP:0009573	Patchy sclerosis of the middle phalanx of the 2nd finger
HP:0009574	Symphalangism of middle phalanx of 2nd finger
HP:0009575	Triangular shaped middle phalanx of the 2nd finger
HP:0009576	Absent middle phalanx of 2nd finger
HP:0009577	Short middle phalanx of the 2nd finger
HP:0009579	Proximal/middle symphalangism of the 2nd finger
HP:0009580	Aplasia/Hypoplasia of the proximal phalanx of the 2nd finger
HP:0009581	Broad proximal phalanx of the 2nd finger
HP:0009582	Bullet-shaped proximal phalanx of the 2nd finger
HP:0009583	Curved proximal phalanx of the 2nd finger
HP:0009584	Osteolytic defects of the proximal phalanx of the 2nd finger
HP:0009585	Patchy sclerosis of the proximal phalanx of the 2nd finger
HP:0009586	Symphalangism affecting the proximal phalanx of the 2nd finger
HP:0009587	Triangular shaped proximal phalanx of the 2nd finger
HP:0009588	Vestibular Schwannoma
HP:0009589	Bilateral vestibular Schwannoma
HP:0009590	Unilateral vestibular Schwannoma
HP:0009591	Abnormality of the vestibulocochlear nerve
HP:0009592	Astrocytoma
HP:0009593	Peripheral Schwannoma
HP:0009594	Retinal hamartoma
HP:0009595	Occasional neurofibromas
HP:0009596	Aplasia of the proximal phalanx of the 2nd finger
HP:0009597	Short proximal phalanx of the 2nd finger
HP:0009598	Symphalangism of the proximal phalanx of the 2nd finger with the 2nd metacarpal
HP:0009599	Abnormality of thumb epiphysis
HP:0009600	Flexion contracture of thumb
HP:0009601	Aplasia/Hypoplasia of the thumb
HP:0009602	Abnormality of thumb phalanx
HP:0009603	Deviation of the thumb
HP:0009606	Complete duplication of distal phalanx of the thumb
HP:0009608	Complete duplication of proximal phalanx of the thumb
HP:0009609	Duplication of the 1st metacarpal
HP:0009611	Bifid distal phalanx of the thumb
HP:0009612	Duplication of the distal phalanx of the thumb
HP:0009613	Duplication of the proximal phalanx of the thumb
HP:0009614	Bifid proximal phalanx of the thumb
HP:0009615	Complete duplication of the first metacarpal
HP:0009616	Bifid first metacarpal
HP:0009617	Abnormality of the distal phalanx of the thumb
HP:0009618	Abnormality of the proximal phalanx of the thumb
HP:0009620	obsolete Radial deviation of the thumb
HP:0009621	obsolete Ulnar deviation of the thumb
HP:0009622	Distally placed thumb
HP:0009623	Proximal placement of thumb
HP:0009624	Contractures of the carpometacarpal joint of the thumb
HP:0009625	Contractures of the metacarpophalangeal joint of the thumb
HP:0009626	Contractures of the interphalangeal joint of the thumb
HP:0009629	Aplasia/Hypoplasia of the proximal phalanx of the thumb
HP:0009630	Broad proximal phalanx of the thumb
HP:0009631	Bullet-shaped proximal phalanx of the thumb
HP:0009632	Curved proximal phalanx of the thumb
HP:0009633	Osteolytic defect of the proximal phalanx of the thumb
HP:0009634	Patchy sclerosis of the proximal phalanx of the thumb
HP:0009635	Synostosis of thumb phalanx
HP:0009636	Triangular shaped proximal phalanx of the thumb
HP:0009637	Absent proximal phalanx of thumb
HP:0009638	Short proximal phalanx of thumb
HP:0009640	Synostosis of the proximal phalanx of the thumb with the 1st metacarpal
HP:0009641	Aplasia/Hypoplasia of the distal phalanx of the thumb
HP:0009642	Broad distal phalanx of the thumb
HP:0009643	Bullet-shaped distal phalanx of the thumb
HP:0009644	Curved distal phalanx of the thumb
HP:0009645	Osteolytic defect of the distal phalanx of the thumb
HP:0009646	Patchy sclerosis of the distal phalanx of the thumb
HP:0009648	Triangular shaped distal phalanx of the thumb
HP:0009649	Aplasia of the distal phalanx of the thumb
HP:0009650	Short distal phalanx of the thumb
HP:0009652	Bullet-shaped thumb phalanx
HP:0009653	Curved thumb phalanx
HP:0009654	Osteolytic defect of thumb phalanx
HP:0009655	Patchy sclerosis of thumb phalanx
HP:0009656	Symphalangism of the thumb
HP:0009657	Triangular shaped thumb phalanx
HP:0009658	Aplasia/Hypoplasia of the phalanges of the thumb
HP:0009659	Partial absence of thumb
HP:0009660	Short phalanx of the thumb
HP:0009662	Abnormality of the epiphysis of the distal phalanx of the thumb
HP:0009663	Abnormality of the epiphysis of the proximal phalanx of the thumb
HP:0009664	Absent epiphysis of the proximal phalanx of the thumb
HP:0009665	Bracket epiphysis of the proximal phalanx of the thumb
HP:0009666	Cone-shaped epiphysis of the proximal phalanx of the thumb
HP:0009667	Enlarged epiphysis of the proximal phalanx of the thumb
HP:0009668	Fragmentation of the epiphysis of the proximal phalanx of the thumb
HP:0009669	Irregular epiphysis of the proximal phalanx of the thumb
HP:0009670	Ivory epiphysis of the proximal phalanx of the thumb
HP:0009671	Pseudoepiphysis of the proximal phalanx of the thumb
HP:0009672	Small epiphysis of the proximal phalanx of the thumb
HP:0009673	Stippling of the epiphysis of the proximal phalanx of the thumb
HP:0009674	Triangular epiphysis of the proximal phalanx of the thumb
HP:0009675	Absent epiphysis of the distal phalanx of the thumb
HP:0009676	Bracket epiphysis of the distal phalanx of the thumb
HP:0009677	Cone-shaped epiphysis of the distal phalanx of the thumb
HP:0009678	Enlarged epiphysis of the distal phalanx of the thumb
HP:0009679	Fragmentation of the epiphysis of the distal phalanx of the thumb
HP:0009680	Irregular epiphysis of the distal phalanx of the thumb
HP:0009681	Ivory epiphysis of the distal phalanx of the thumb
HP:0009682	Pseudoepiphysis of the distal phalanx of the thumb
HP:0009683	Small epiphysis of the distal phalanx of the thumb
HP:0009684	Stippling of the epiphysis of the distal phalanx of the thumb
HP:0009685	Triangular epiphysis of the distal phalanx of the thumb
HP:0009686	Absent epiphyses of the thumb
HP:0009687	Bracket epiphyses of the thumb
HP:0009688	Cone-shaped epiphysis of the thumb
HP:0009689	Enlarged thumb epiphysis
HP:0009690	Fragmentation of thumb epiphysis
HP:0009691	Irregular thumb epiphysis
HP:0009692	Ivory epiphysis of the thumb
HP:0009693	Pseudoepiphysis of the thumb
HP:0009694	Small thumb epiphysis
HP:0009695	Stippling of thumb epiphysis
HP:0009696	Triangular epiphyses of the thumb
HP:0009697	Contracture of the distal interphalangeal joint of the fingers
HP:0009699	Osteolytic defects of the hand bones
HP:0009700	Finger symphalangism
HP:0009701	Metacarpal synostosis
HP:0009702	Carpal synostosis
HP:0009703	Synostosis involving the 1st metacarpal
HP:0009704	Chronic CSF lymphocytosis
HP:0009705	Synostosis involving the 2nd metacarpal
HP:0009706	Synostosis involving the 3rd metacarpal
HP:0009707	Synostosis involving the 4th metacarpal
HP:0009708	Synostosis involving the 5th metacarpal
HP:0009709	Increased CSF interferon alpha
HP:0009710	Chilblains
HP:0009711	Retinal capillary hemangioma
HP:0009713	Spinal hemangioblastoma
HP:0009714	Abnormality of the epididymis
HP:0009715	Papillary cystadenoma of the epididymis
HP:0009716	Subependymal nodules
HP:0009717	Cortical tubers
HP:0009718	Subependymal giant-cell astrocytoma
HP:0009719	Hypomelanotic macule
HP:0009720	Adenoma sebaceum
HP:0009721	Shagreen patch
HP:0009722	Dental enamel pits
HP:0009723	Abnormality of the subungual region
HP:0009724	Subungual fibromas
HP:0009725	Bladder neoplasm
HP:0009726	Renal neoplasm
HP:0009727	Achromatic retinal patches
HP:0009728	Neoplasm of striated muscle
HP:0009729	Cardiac rhabdomyoma
HP:0009730	Rhabdomyoma
HP:0009731	Cerebral hamartoma
HP:0009732	Plexiform neurofibroma
HP:0009733	Glioma
HP:0009734	Optic nerve glioma
HP:0009735	Spinal neurofibromas
HP:0009736	Tibial pseudoarthrosis
HP:0009737	Lisch nodules
HP:0009738	Abnormality of the antihelix
HP:0009739	Hypoplasia of the antihelix
HP:0009740	Aplasia of the parotid gland
HP:0009741	Nephrosclerosis
HP:0009742	Stiff shoulders
HP:0009743	Distichiasis
HP:0009744	Abnormal spinal dura mater morphology
HP:0009745	Spinalarachnoid cyst
HP:0009746	Thick nasal septum
HP:0009747	Lumbosacral hirsutism
HP:0009748	Large earlobe
HP:0009751	Aplasia of the pectoralis major muscle
HP:0009752	Cleft in skull base
HP:0009754	Fibrous syngnathia
HP:0009755	Ankyloblepharon
HP:0009756	Popliteal pterygium
HP:0009757	Intercrural pterygium
HP:0009758	Pyramidal skinfold extending from the base to the top of the nails
HP:0009759	Neck pterygia
HP:0009760	Antecubital pterygium
HP:0009761	Anterior clefting of vertebral bodies
HP:0009762	Facial wrinkling
HP:0009763	Limb pain
HP:0009765	Low hanging columella
HP:0009767	Aplasia/Hypoplasia of the phalanges of the hand
HP:0009768	Broad phalanges of the hand
HP:0009769	Bullet-shaped phalanges of the hand
HP:0009770	Curved phalanges of the hand
HP:0009771	Osteolytic defects of the phalanges of the hand
HP:0009772	Patchy sclerosis of finger phalanx
HP:0009773	Symphalangism affecting the phalanges of the hand
HP:0009774	Triangular shaped phalanges of the hand
HP:0009775	Amniotic constriction ring
HP:0009776	Adactyly
HP:0009777	Absent thumb
HP:0009778	Short thumb
HP:0009779	3-4 toe syndactyly
HP:0009780	Iliac horns
HP:0009781	Lester's sign
HP:0009782	Aplasia/Hypoplasia of the biceps
HP:0009783	Biceps aplasia
HP:0009784	Aplasia/Hypoplasia of the triceps
HP:0009785	Triceps aplasia
HP:0009786	Aplasia/Hypoplasia of the musculature of the thigh
HP:0009787	Aplasia/Hypoplasia of the quadriceps
HP:0009788	Quadriceps aplasia
HP:0009789	Perianal abscess
HP:0009790	Hemisacrum
HP:0009791	Bifid sacrum
HP:0009792	Teratoma
HP:0009793	Presacral teratoma
HP:0009794	Branchial anomaly
HP:0009795	Branchial fistula
HP:0009796	Branchial cyst
HP:0009797	Cholesteatoma
HP:0009798	Euthyroid goiter
HP:0009799	Supernumerary spleens
HP:0009800	Maternal diabetes
HP:0009802	Aplasia of the phalanges of the hand
HP:0009803	Short phalanx of finger
HP:0009804	Reduced number of teeth
HP:0009805	Low-output congestive heart failure
HP:0009806	Nephrogenic diabetes insipidus
HP:0009808	Anomaly of the upper limb diaphyses
HP:0009809	Abnormality of upper limb metaphysis
HP:0009810	Abnormality of upper limb joint
HP:0009811	Abnormality of the elbow
HP:0009812	Amelia involving the upper limbs
HP:0009813	Upper limb phocomelia
HP:0009814	Upper limb peromelia
HP:0009815	Aplasia/hypoplasia of the extremities
HP:0009816	Lower limb undergrowth
HP:0009817	Aplasia involving bones of the lower limbs
HP:0009818	Amelia involving the lower limbs
HP:0009819	Lower limb phocomelia
HP:0009820	Lower limb peromelia
HP:0009821	Forearm undergrowth
HP:0009822	Aplasia involving forearm bones
HP:0009823	Aplasia involving bones of the upper limbs
HP:0009824	Upper limb undergrowth
HP:0009825	Aplasia involving bones of the extremities
HP:0009826	Limb undergrowth
HP:0009827	Amelia
HP:0009828	Peromelia
HP:0009829	Phocomelia
HP:0009830	Peripheral neuropathy
HP:0009831	Mononeuropathy
HP:0009832	Abnormal distal phalanx morphology of finger
HP:0009833	Abnormal middle phalanx morphology of the hand
HP:0009834	Abnormal proximal phalanx morphology of the hand
HP:0009835	Aplasia/Hypoplasia of the distal phalanges of the hand
HP:0009836	Broad distal phalanx of finger
HP:0009837	Bullet-shaped distal phalanges of the hand
HP:0009838	Curved distal phalanges of the hand
HP:0009839	Osteolytic defects of the distal phalanges of the hand
HP:0009840	Patchy sclerosis of distal phalanx of finger
HP:0009843	Aplasia/Hypoplasia of the middle phalanges of the hand
HP:0009844	Broad middle phalanx of finger
HP:0009845	Bullet-shaped middle phalanges of the hand
HP:0009846	Curved middle phalanges of the hand
HP:0009847	Osteolytic defects of the middle phalanges of the hand
HP:0009848	Patchy sclerosis of middle phalanx of finger
HP:0009849	Symphalangism of middle phalanx of finger
HP:0009850	Triangular shaped middle phalanges of the hand
HP:0009851	Aplasia/Hypoplasia of the proximal phalanges of the hand
HP:0009852	Broad proximal phalanges of the hand
HP:0009853	Bullet-shaped proximal phalanges of the hand
HP:0009854	Curved proximal phalanges of the hand
HP:0009855	Osteolytic defects of the proximal phalanges of the hand
HP:0009856	Patchy sclerosis of proximal phalanx of finger
HP:0009857	Symphalangism affecting the proximal phalanges of the hand
HP:0009858	Triangular shaped proximal phalanges of the hand
HP:0009875	Triangular shaped distal phalanges of the hand
HP:0009878	Cerebellar ataxia associated with quadrupedal gait
HP:0009879	Cortical gyral simplification
HP:0009880	Broad distal phalanges of all fingers
HP:0009881	Aplasia of the distal phalanges of the hand
HP:0009882	Short distal phalanx of finger
HP:0009883	Duplication of the distal phalanx of hand
HP:0009884	Tapered distal phalanges of finger
HP:0009885	obsolete Prenatal short stature
HP:0009886	Trichorrhexis nodosa
HP:0009887	Abnormality of hair pigmentation
HP:0009888	Abnormality of secondary sexual hair
HP:0009889	Localized hirsutism
HP:0009890	High anterior hairline
HP:0009891	Underdeveloped supraorbital ridges
HP:0009892	Anotia
HP:0009893	Telangiectasia of the ear
HP:0009894	Thickened ears
HP:0009895	Abnormality of the crus of the helix
HP:0009896	Abnormality of the antitragus
HP:0009897	Horizontal crus of helix
HP:0009898	Underdeveloped crus of the helix
HP:0009899	Prominent crus of helix
HP:0009900	Unilateral deafness
HP:0009901	Crumpled ear
HP:0009902	Cleft helix
HP:0009903	Conjunctival nodule
HP:0009904	Prominent ear helix
HP:0009905	Thin ear helix
HP:0009906	Aplasia/Hypoplasia of the earlobes
HP:0009907	Attached earlobe
HP:0009908	Anterior creases of earlobe
HP:0009909	Uplifted earlobe
HP:0009910	Aplasia of the middle ear ossicles
HP:0009911	Abnormal temporal bone morphology
HP:0009912	Abnormality of the tragus
HP:0009913	Aplasia/Hypoplasia of the tragus
HP:0009914	Cyclopia
HP:0009915	Corneal asymmetry
HP:0009916	Anisocoria
HP:0009917	Persistent pupillary membrane
HP:0009918	Ectopia pupillae
HP:0009919	Retinoblastoma
HP:0009920	Nevus of Ota
HP:0009921	Duane anomaly
HP:0009922	Vascular remnant arising from the disc
HP:0009924	Aplasia/Hypoplasia involving the nose
HP:0009926	Epiphora
HP:0009927	Aplasia of the nose
HP:0009928	Thick nasal alae
HP:0009929	Abnormality of the columella
HP:0009930	Asymmetry of the nares
HP:0009931	Enlarged naris
HP:0009932	Single naris
HP:0009933	Narrow naris
HP:0009934	Supernumerary naris
HP:0009935	Aplasia/Hypoplasia of the nasal septum
HP:0009936	Narrow nasal septum
HP:0009937	Facial hirsutism
HP:0009938	Sunken cheeks
HP:0009939	Mandibular aplasia
HP:0009940	Asymmetry of the mandible
HP:0009941	Asymmetry of the mouth
HP:0009942	Duplication of thumb phalanx
HP:0009943	Complete duplication of thumb phalanx
HP:0009944	Partial duplication of thumb phalanx
HP:0009945	Duplication of phalanx of 2nd finger
HP:0009946	Polydactyly affecting the 2nd finger
HP:0009947	Duplication of the proximal phalanx of the 2nd finger
HP:0009948	Duplication of the distal phalanx of the 2nd finger
HP:0009949	Duplication of the middle phalanx of the 2nd finger
HP:0009950	Complete duplication of the distal phalanx of the 2nd finger
HP:0009951	Partial duplication of the distal phalanx of the 2nd finger
HP:0009952	Complete duplication of the middle phalanx of the 2nd finger
HP:0009953	Partial duplication of the middle phalanx of the 2nd finger
HP:0009954	Complete duplication of the proximal phalanx of the 2nd finger
HP:0009955	Partial duplication of the proximal phalanx of the 2nd finger
HP:0009956	Partial duplication of the phalanges of the 2nd finger
HP:0009957	Complete duplication of the phalanges of the 2nd finger
HP:0009958	Polydactyly affecting the 3rd finger
HP:0009959	Duplication of phalanx of 3rd finger
HP:0009960	Complete duplication of the phalanges of the 3rd finger
HP:0009961	Partial duplication of the phalanges of the 3rd finger
HP:0009962	Duplication of the distal phalanx of the 3rd finger
HP:0009963	Duplication of the middle phalanx of the 3rd finger
HP:0009964	Duplication of the proximal phalanx of the 3rd finger
HP:0009965	Complete duplication of the distal phalanx of the 3rd finger
HP:0009966	Complete duplication of the middle phalanx of the 3rd finger
HP:0009967	Complete duplication of the proximal phalanx of the 3rd finger
HP:0009968	Partial duplication of the distal phalanx of the 3rd finger
HP:0009969	Partial duplication of the middle phalanx of the 3rd finger
HP:0009970	Partial duplication of the proximal phalanx of the 3rd finger
HP:0009971	Polydactyly affecting the 4th finger
HP:0009972	Duplication of phalanx of 4th finger
HP:0009973	Complete duplication of the phalanges of the 4th finger
HP:0009974	Partial duplication of the phalanges of the 4th finger
HP:0009975	Duplication of the distal phalanx of the 4th finger
HP:0009976	Duplication of the middle phalanx of the 4th finger
HP:0009977	Duplication of the proximal phalanx of the 4th finger
HP:0009978	Complete duplication of the distal phalanx of the 4th finger
HP:0009979	Complete duplication of the middle phalanx of the 4th finger
HP:0009980	Complete duplication of the proximal phalanx of the 4th finger
HP:0009981	Partial duplication of the distal phalanx of the 4th finger
HP:0009982	Partial duplication of the middle phalanx of the 4th finger
HP:0009983	Partial duplication of the proximal phalanx of the 4th finger
HP:0009985	Duplication of phalanx of 5th finger
HP:0009986	Complete duplication of the phalanges of the 5th finger
HP:0009987	Partial duplication of the phalanges of the 5th finger
HP:0009988	Duplication of the distal phalanx of the 5th finger
HP:0009989	Duplication of the middle phalanx of the 5th finger
HP:0009990	Duplication of the proximal phalanx of the 5th finger
HP:0009991	Complete duplication of the distal phalanx of the 5th finger
HP:0009992	Complete duplication of the middle phalanx of the 5th finger
HP:0009993	Complete duplication of the proximal phalanx of the 5th finger
HP:0009994	Partial duplication of the distal phalanx of the 5th finger
HP:0009995	Partial duplication of the middle phalanx of the 5th finger
HP:0009996	Partial duplication of the proximal phalanx of the 5th finger
HP:0009997	Duplication of phalanx of hand
HP:0009998	Complete duplication of phalanx of hand
HP:0009999	Partial duplication of the phalanx of hand
HP:0010000	Complete duplication of the proximal phalanges of the hand
HP:0010001	Complete duplication of the distal phalanges of the hand
HP:0010002	Complete duplication of the middle phalanges of the hand
HP:0010003	Partial duplication of the proximal phalanges of the hand
HP:0010004	Partial duplication of the distal phalanges of the hand
HP:0010005	Partial duplication of the middle phalanges of the hand
HP:0010006	Duplication of the proximal phalanx of hand
HP:0010008	Duplication of the middle phalanx of hand
HP:0010009	Abnormality of the 1st metacarpal
HP:0010010	Abnormality of the 2nd metacarpal
HP:0010011	Abnormality of the 3rd metacarpal
HP:0010012	Abnormality of the 4th metacarpal
HP:0010013	Abnormality of the 5th metacarpal
HP:0010014	Abnormality of the epiphysis of the 1st metacarpal
HP:0010015	Absent epiphysis of the 1st metacarpal
HP:0010016	Bracket epiphysis of the 1st metacarpal
HP:0010017	Cone-shaped epiphysis of the 1st metacarpal
HP:0010018	Enlarged epiphysis of the 1st metacarpal
HP:0010019	Fragmentation of the epiphysis of the 1st metacarpal
HP:0010020	Irregular epiphysis of the 1st metacarpal
HP:0010021	Ivory epiphysis of the 1st metacarpal
HP:0010022	Pseudoepiphysis of the 1st metacarpal
HP:0010023	Small epiphysis of the 1st metacarpal
HP:0010024	Epiphyseal stippling of the first metacarpal
HP:0010025	Triangular epiphysis of the 1st metacarpal
HP:0010026	Aplasia/Hypoplasia of the 1st metacarpal
HP:0010027	Broad 1st metacarpal
HP:0010028	Bullet-shaped 1st metacarpal
HP:0010029	Curved 1st metacarpal
HP:0010030	Osteolytic defects of the 1st metacarpal
HP:0010031	Patchy sclerosis of the 1st metacarpal
HP:0010033	Triangular shaped 1st metacarpal
HP:0010034	Short 1st metacarpal
HP:0010035	Aplasia of the 1st metacarpal
HP:0010036	Aplasia/Hypoplasia of the 2nd metacarpal
HP:0010037	Aplasia of the 2nd metacarpal
HP:0010038	Short 2nd metacarpal
HP:0010039	Aplasia/Hypoplasia of the 3rd metacarpal
HP:0010040	Aplasia of the 3rd metacarpal
HP:0010041	Short 3rd metacarpal
HP:0010042	Aplasia/Hypoplasia of the 4th metacarpal
HP:0010043	Aplasia of the 4th metacarpal
HP:0010044	Short 4th metacarpal
HP:0010045	Aplasia/Hypoplasia of the 5th metacarpal
HP:0010046	Aplasia of the 5th metacarpal
HP:0010047	Short 5th metacarpal
HP:0010048	Aplasia of metacarpal bones
HP:0010049	Short metacarpal
HP:0010051	Deviation of the hallux
HP:0010052	Abnormality of the proximal phalanx of the hallux
HP:0010053	Abnormality of the distal phalanx of the hallux
HP:0010054	Abnormality of the first metatarsal bone
HP:0010055	Broad hallux
HP:0010056	Abnormality of the epiphyses of the hallux
HP:0010057	Abnormality of the phalanges of the hallux
HP:0010058	Aplasia/Hypoplasia of the phalanges of the hallux
HP:0010059	Broad hallux phalanx
HP:0010060	Bullet-shaped hallux phalanx
HP:0010061	Curved hallux phalanx
HP:0010062	Osteolytic defects of the phalanges of the hallux
HP:0010063	Patchy sclerosis of hallux phalanx
HP:0010064	Symphalangism affecting the phalanges of the hallux
HP:0010065	Triangular shaped phalanges of the hallux
HP:0010066	Duplication of phalanx of hallux
HP:0010067	Aplasia/hypoplasia of the 1st metatarsal
HP:0010068	Broad first metatarsal
HP:0010069	Bullet-shaped 1st metatarsal
HP:0010070	Curved 1st metatarsal
HP:0010071	Osteolytic defects of the 1st metatarsal
HP:0010072	Patchy sclerosis of the 1st metatarsal
HP:0010073	Synostosis involving the 1st metatarsal
HP:0010074	Triangular shaped 1st metatarsal
HP:0010075	Duplication of the 1st metatarsal
HP:0010076	Aplasia/Hypoplasia of the distal phalanx of the hallux
HP:0010077	Broad distal phalanx of the hallux
HP:0010078	Bullet-shaped distal phalanx of the hallux
HP:0010079	Curved distal phalanx of the hallux
HP:0010080	Osteolytic defects of the distal phalanx of the hallux
HP:0010081	Patchy sclerosis of the distal phalanx of the hallux
HP:0010082	Symphalangism affecting the distal phalanx of the hallux
HP:0010083	Triangular shaped distal phalanx of the hallux
HP:0010084	Duplication of the distal phalanx of the hallux
HP:0010085	Aplasia/Hypoplasia of the proximal phalanx of the hallux
HP:0010086	Broad proximal phalanx of the hallux
HP:0010087	Bullet-shaped proximal phalanx of the hallux
HP:0010088	Curved proximal phalanx of the hallux
HP:0010089	Osteolytic defects of the proximal phalanx of the hallux
HP:0010090	Patchy sclerosis of the proximal phalanx of the hallux
HP:0010091	Symphalangism affecting the proximal phalanx of the hallux
HP:0010092	Triangular shaped proximal phalanx of the hallux
HP:0010093	Duplication of the proximal phalanx of the hallux
HP:0010094	Complete duplication of the proximal phalanx of the hallux
HP:0010095	Partial duplication of the proximal phalanx of the hallux
HP:0010096	Complete duplication of the distal phalanx of the hallux
HP:0010097	Partial duplication of the distal phalanx of the hallux
HP:0010098	Complete duplication of the 1st metatarsal
HP:0010099	Partial duplication of the 1st metatarsal
HP:0010100	Complete duplication of hallux phalanx
HP:0010101	Partial duplication of the phalanges of the hallux
HP:0010102	Aplasia of the distal phalanx of the hallux
HP:0010103	Short distal phalanx of hallux
HP:0010104	Absent first metatarsal
HP:0010105	Short first metatarsal
HP:0010106	Aplasia of the proximal phalanx of the hallux
HP:0010107	Short proximal phalanx of hallux
HP:0010109	Short hallux
HP:0010110	Aplasia of the phalanges of the hallux
HP:0010111	Short phalanx of hallux
HP:0010112	Mesoaxial foot polydactyly
HP:0010113	Absent hallux epiphysis
HP:0010114	Bracket epiphyses of the hallux
HP:0010115	Cone-shaped epiphyses of the hallux
HP:0010116	Enlarged epiphyses of the hallux
HP:0010117	Fragmentation of the epiphyses of the hallux
HP:0010118	Irregular epiphyses of the hallux
HP:0010119	Ivory epiphyses of the hallux
HP:0010120	Pseudoepiphyses of the hallux
HP:0010121	Small epiphyses of the hallux
HP:0010122	Stippling of the epiphyses of the hallux
HP:0010123	Triangular epiphyses of the hallux
HP:0010124	Abnormality of the epiphysis of the distal phalanx of the hallux
HP:0010125	Abnormality of the epiphysis of the 1st metatarsal
HP:0010126	Abnormality of the epiphysis of the proximal phalanx of the hallux
HP:0010127	Absent epiphysis of the proximal phalanx of the hallux
HP:0010128	Bracket epiphysis of the proximal phalanx of the hallux
HP:0010129	Cone-shaped epiphysis of the proximal phalanx of the hallux
HP:0010130	Enlarged epiphysis of the proximal phalanx of the hallux
HP:0010131	Fragmentation of the epiphysis of the proximal phalanx of the hallux
HP:0010132	Irregular epiphysis of the proximal phalanx of the hallux
HP:0010133	Ivory epiphysis of the proximal phalanx of the hallux
HP:0010134	Pseudoepiphysis of the proximal phalanx of the hallux
HP:0010135	Small epiphysis of the proximal phalanx of the hallux
HP:0010136	Stippling of the epiphysis of the proximal phalanx of the hallux
HP:0010137	Triangular epiphysis of the proximal phalanx of the hallux
HP:0010138	Absent epiphysis of the distal phalanx of the hallux
HP:0010139	Bracket epiphysis of the distal phalanx of the hallux
HP:0010140	Cone-shaped epiphysis of the distal phalanx of the hallux
HP:0010141	Enlarged epiphysis of the distal phalanx of the hallux
HP:0010142	Fragmentation of the epiphysis of the distal phalanx of the hallux
HP:0010143	Irregular epiphysis of the distal phalanx of the hallux
HP:0010144	Ivory epiphysis of the distal phalanx of the hallux
HP:0010145	Pseudoepiphysis of the distal phalanx of the hallux
HP:0010146	Small epiphysis of the distal phalanx of the hallux
HP:0010147	Stippling of the epiphysis of the distal phalanx of the hallux
HP:0010148	Triangular epiphysis of the distal phalanx of the hallux
HP:0010149	Absent epiphysis of the 1st metatarsal
HP:0010150	Bracket epiphysis of the 1st metatarsal
HP:0010151	Cone-shaped epiphysis of the 1st metatarsal
HP:0010152	Enlarged epiphysis of the 1st metatarsal
HP:0010153	Fragmentation of the epiphysis of the 1st metatarsal
HP:0010154	Irregular epiphysis of the 1st metatarsal
HP:0010155	Ivory epiphysis of the 1st metatarsal
HP:0010156	Pseudoepiphysis of the 1st metatarsal
HP:0010157	Small epiphysis of the 1st metatarsal
HP:0010158	Stippling of the epiphysis of the 1st metatarsal
HP:0010159	Triangular epiphysis of the 1st metatarsal
HP:0010160	Abnormality of the epiphyses of the toes
HP:0010161	Abnormality of the phalanges of the toes
HP:0010162	Absent epiphyses of the toes
HP:0010163	Bracket epiphyses of the toes
HP:0010164	Cone-shaped epiphyses of the toes
HP:0010165	Enlarged epiphyses of the toes
HP:0010166	Fragmentation of the epiphyses of the toes
HP:0010167	Irregular epiphyses of the toes
HP:0010168	Ivory epiphyses of the toes
HP:0010169	Pseudoepiphyses of the toes
HP:0010170	Small epiphyses of the toes
HP:0010171	Epiphyseal stippling of toe phalanges
HP:0010172	Triangular epiphyses of the toes
HP:0010173	Aplasia/Hypoplasia of the phalanges of the toes
HP:0010174	Broad phalanx of the toes
HP:0010175	Bullet-shaped toe phalanx
HP:0010176	Curved toe phalanx
HP:0010177	Osteolytic defects of the phalanges of the toes
HP:0010178	Patchy sclerosis of toe phalanx
HP:0010179	Symphalangism affecting the phalanges of the toes
HP:0010180	Triangular shaped phalanges of the toes
HP:0010181	Duplication of phalanx of toe
HP:0010182	Abnormality of the distal phalanges of the toes
HP:0010183	Abnormality of the middle phalanges of the toes
HP:0010184	Abnormality of toe proximal phalanx
HP:0010185	Aplasia/Hypoplasia of the distal phalanges of the toes
HP:0010186	Broad distal phalanx of the toes
HP:0010187	Bullet-shaped distal toe phalanx
HP:0010188	Curved distal toe phalanx
HP:0010189	Osteolytic defects of the distal phalanges of the toes
HP:0010190	Patchy sclerosis of distal toe phalanx
HP:0010191	Symphalangism affecting the distal phalanges of the toes
HP:0010192	Triangular shaped distal phalanges of the toes
HP:0010193	Duplication of distal phalanx of toe
HP:0010194	Aplasia/Hypoplasia of the middle phalanges of the toes
HP:0010195	Broad middle phalanges of the toes
HP:0010196	Bullet-shaped middle toe phalanx
HP:0010197	Curved middle toe phalanx
HP:0010198	Osteolytic defects of the middle phalanges of the toes
HP:0010199	Patchy sclerosis of middle toe phalanx
HP:0010200	Symphalangism affecting the middle phalanges of the toes
HP:0010201	Triangular shaped middle phalanges of the toes
HP:0010202	Duplication of middle phalanx of toe
HP:0010203	Aplasia/hypoplasia of proximal toe phalanx
HP:0010204	Broad proximal phalanx of toe
HP:0010205	Bullet-shaped proximal toe phalanx
HP:0010206	Curved proximal toe phalanx
HP:0010207	Osteolytic defect of the proximal toe phalanx
HP:0010208	Patchy sclerosis of proximal toe phalanx
HP:0010209	Symphalangism affecting the proximal phalanges of the toes
HP:0010210	Triangular shaped proximal phalanges of the toes
HP:0010211	Duplication of proximal phalanx of toe
HP:0010212	Flexion contracture of the hallux
HP:0010213	Contracture of the tarsometatarsal joint of the hallux
HP:0010214	Contracture of the interphalangeal joint of the hallux
HP:0010215	Contractures of the metatarsophalangeal joint of the hallux
HP:0010219	Structural foot deformity
HP:0010220	Abnormality of the epiphysis of the 2nd metacarpal
HP:0010221	Pseudoepiphysis of the 2nd metacarpal
HP:0010222	Abnormality of the epiphysis of the 3rd metacarpal
HP:0010223	Pseudoepiphysis of the 3rd metacarpal
HP:0010224	Abnormality of the epiphysis of the 4th metacarpal
HP:0010225	Pseudoepiphysis of the 4th metacarpal
HP:0010226	Abnormality of the epiphysis of the 5th metacarpal
HP:0010227	Pseudoepiphysis of the 5th metacarpal
HP:0010228	Absent epiphyses of the phalanges of the hand
HP:0010229	Bracket epiphyses of the phalanges of the hand
HP:0010230	Cone-shaped epiphyses of the phalanges of the hand
HP:0010231	Enlarged epiphyses of the phalanges of the hand
HP:0010232	Fragmentation of the epiphyses of the phalanges of the hand
HP:0010233	Irregular epiphyses of the phalanges of the hand
HP:0010234	Ivory epiphyses of the phalanges of the hand
HP:0010235	Pseudoepiphyses of the phalanges of the hand
HP:0010236	Small epiphyses of the phalanges of the hand
HP:0010237	Epiphyseal stippling of finger phalanges
HP:0010238	Triangular epiphyses of the phalanges of the hand
HP:0010239	Aplasia of the middle phalanx of the hand
HP:0010241	Short proximal phalanx of finger
HP:0010242	Aplasia of the proximal phalanges of the hand
HP:0010243	Abnormality of the epiphyses of the distal phalanx of finger
HP:0010244	Abnormality of the epiphyses of the middle phalanges of the hand
HP:0010245	Abnormality of the epiphyses of the proximal phalanges of the hand
HP:0010246	Absent epiphyses of the distal phalanges of the hand
HP:0010247	Bracket epiphyses of the distal phalanges of the hand
HP:0010248	Cone-shaped epiphyses of the distal phalanges of the hand
HP:0010249	Enlarged epiphyses of the distal phalanges of the hand
HP:0010250	Fragmentation of the epiphyses of the distal phalanges of the hand
HP:0010251	Irregular epiphyses of the distal phalanges of the hand
HP:0010252	Ivory epiphyses of the distal phalanges of the hand
HP:0010253	Pseudoepiphyses of the distal phalanges of the hand
HP:0010254	Small epiphyses of the distal phalanges of the hand
HP:0010255	Stippling of the epiphyses of the distal phalanges of the hand
HP:0010256	Triangular epiphyses of the distal phalanges of the hand
HP:0010257	Absent epiphyses of the middle phalanges of the hand
HP:0010258	Bracket epiphyses of the middle phalanges of the hand
HP:0010259	Cone-shaped epiphyses of the middle phalanges of the hand
HP:0010260	Enlarged epiphyses of the middle phalanges of the hand
HP:0010261	Fragmentation of the epiphyses of the middle phalanges of the hand
HP:0010262	Irregular epiphyses of the middle phalanges of the hand
HP:0010263	Ivory epiphyses of the middle phalanges of the hand
HP:0010264	Pseudoepiphyses of the middle phalanges of the hand
HP:0010265	Small epiphyses of the middle phalanges of the hand
HP:0010266	Stippling of the epiphyses of the middle phalanges of the hand
HP:0010267	Triangular epiphyses of the middle phalanges of the hand
HP:0010268	Absent epiphyses of the proximal phalanges of the hand
HP:0010269	Bracket epiphyses of the proximal phalanges of the hand
HP:0010270	Cone-shaped epiphyses of the proximal phalanges of the hand
HP:0010271	Enlarged epiphyses of the proximal phalanges of the hand
HP:0010272	Fragmentation of the epiphyses of the proximal phalanges of the hand
HP:0010273	Irregular epiphyses of the proximal phalanges of the hand
HP:0010274	Ivory epiphyses of the proximal phalanges of the hand
HP:0010275	Pseudoepiphyses of the proximal phalanges of the hand
HP:0010276	Small epiphyses of the proximal phalanges of the hand
HP:0010277	Stippling of the epiphyses of the proximal phalanges of the hand
HP:0010278	Triangular epiphyses of the proximal phalanges of the hand
HP:0010280	Stomatitis
HP:0010281	Cleft lower lip
HP:0010282	Thin lower lip vermilion
HP:0010284	Intra-oral hyperpigmentation
HP:0010285	Oral synechia
HP:0010286	Abnormal salivary gland morphology
HP:0010287	Abnormality of the submandibular glands
HP:0010288	Abnormality of the sublingual glands
HP:0010289	Cleft of alveolar ridge of maxilla
HP:0010290	Short hard palate
HP:0010291	Prominent palatine ridges
HP:0010292	Absent uvula
HP:0010293	Aplasia/Hypoplasia of the uvula
HP:0010294	Palate fistula
HP:0010295	Aplasia/Hypoplasia of the tongue
HP:0010296	Ankyloglossia
HP:0010297	Bifid tongue
HP:0010298	Smooth tongue
HP:0010299	Abnormality of dentin
HP:0010300	Abnormally low-pitched voice
HP:0010301	Spinal dysraphism
HP:0010302	Spinal cord tumor
HP:0010303	Abnormal spinal meningeal morphology
HP:0010304	Spinal meningeal diverticulum
HP:0010305	Absence of the sacrum
HP:0010306	Short thorax
HP:0010307	Stridor
HP:0010308	Asternia
HP:0010309	Bifid sternum
HP:0010310	Chylothorax
HP:0010311	Aplasia/Hypoplasia of the breasts
HP:0010312	Asymmetry of the breasts
HP:0010313	Breast hypertrophy
HP:0010314	Premature thelarche
HP:0010315	Aplasia/Hypoplasia of the diaphragm
HP:0010316	Ebstein anomaly of the tricuspid valve
HP:0010317	Scapular aplasia
HP:0010318	Aplasia/Hypoplasia of the abdominal wall musculature
HP:0010319	Abnormality of the 2nd toe
HP:0010320	Abnormality of the 3rd toe
HP:0010321	Abnormality of the 4th toe
HP:0010322	Abnormality of the 5th toe
HP:0010323	Abnormality of the epiphyses of the 2nd toe
HP:0010324	Abnormality of phalanx of the 2nd toe
HP:0010325	Aplasia/Hypoplasia of the 2nd toe
HP:0010326	Deviation of the 2nd toe
HP:0010327	Flexion contracture of the 2nd toe
HP:0010328	Polydactyly affecting the 2nd toe
HP:0010329	Abnormality of the epiphyses of the 3rd toe
HP:0010330	Abnormality of the phalanges of the 3rd toe
HP:0010331	Aplasia/Hypoplasia of the 3rd toe
HP:0010332	Deviation of the 3rd toe
HP:0010333	Flexion contracture of 3rd toe
HP:0010334	Polydactyly affecting the 3rd toe
HP:0010335	Abnormality of the epiphyses of the 4th toe
HP:0010336	Abnormality of the phalanges of the 4th toe
HP:0010337	Aplasia/Hypoplasia of the 4th toe
HP:0010338	Deviation of the 4th toe
HP:0010339	Flexion contracture of the 4th toe
HP:0010340	Polydactyly affecting the 4th toe
HP:0010341	Abnormality of the epiphyses of the 5th toe
HP:0010342	Abnormality of the phalanges of the 5th toe
HP:0010343	Aplasia/Hypoplasia of the 5th toe
HP:0010344	Deviation of the 5th toe
HP:0010345	Flexion contracture of the 5th toe
HP:0010347	Aplasia/Hypoplasia of the phalanges of the 2nd toe
HP:0010348	Broad phalanges of the 2nd toe
HP:0010349	Bullet-shaped 2nd toe phalanx
HP:0010350	Curved 2nd toe phalanx
HP:0010351	Osteolytic defects of the phalanges of the 2nd toe
HP:0010352	Patchy sclerosis of 2nd toe phalanx
HP:0010353	Symphalangism affecting the phalanges of the 2nd toe
HP:0010354	Triangular shaped phalanges of the 2nd toe
HP:0010355	Duplication of the phalanges of the 2nd toe
HP:0010356	Abnormality of the distal phalanx of the 2nd toe
HP:0010357	Abnormality of the middle phalanx of the 2nd toe
HP:0010358	Abnormality of the proximal phalanx of the 2nd toe
HP:0010359	Aplasia/Hypoplasia of the phalanges of the 3rd toe
HP:0010360	Broad phalanges of the 3rd toe
HP:0010361	Bullet-shaped 3rd toe phalanx
HP:0010362	Curved 3rd toe phalanx
HP:0010363	Osteolytic defects of the phalanges of the 3rd toe
HP:0010364	Patchy sclerosis of 3rd toe phalanx
HP:0010365	Symphalangism affecting the phalanges of the 3rd toe
HP:0010366	Triangular shaped phalanges of the 3rd toe
HP:0010367	Duplication of phalanx of the 3rd toe
HP:0010368	Abnormality of the distal phalanx of the 3rd toe
HP:0010369	Abnormality of the middle phalanx of the 3rd toe
HP:0010370	Abnormality of the proximal phalanx of the 3rd toe
HP:0010371	Aplasia/Hypoplasia of the phalanges of the 4th toe
HP:0010372	Broad phalanges of the 4th toe
HP:0010373	Bullet-shaped 4th toe phalanx
HP:0010374	Curved 4th toe phalanx
HP:0010375	Osteolytic defects of the phalanges of the 4th toe
HP:0010376	Patchy sclerosis of 4th toe phalanx
HP:0010377	Symphalangism affecting the phalanges of the 4th toe
HP:0010378	Triangular shaped phalanges of the 4th toe
HP:0010379	Duplication of phalanx of the 4th toe
HP:0010380	Abnormality of the distal phalanx of the 4th toe
HP:0010381	Abnormality of the middle phalanx of the 4th toe
HP:0010382	Abnormality of the proximal phalanx of the 4th toe
HP:0010383	Aplasia/Hypoplasia of the phalanges of the 5th toe
HP:0010384	Broad phalanges of the 5th toe
HP:0010385	Bullet-shaped 5th toe phalanx
HP:0010386	Curved 5th toe phalanx
HP:0010387	Osteolytic defects of the phalanges of the 5th toe
HP:0010388	Patchy sclerosis of 5th toe phalanx
HP:0010389	Symphalangism affecting the phalanges of the 5th toe
HP:0010390	Triangular shaped phalanges of the 5th toe
HP:0010391	Duplication of the phalanges of the 5th toe
HP:0010392	Abnormality of the distal phalanx of the 5th toe
HP:0010393	Abnormality of the middle phalanx of the 5th toe
HP:0010394	Abnormality of the proximal phalanx of the 5th toe
HP:0010395	Aplasia/hypoplasia of the proximal phalanx of the 2nd toe
HP:0010396	Broad proximal phalanx of the 2nd toe
HP:0010397	Bullet-shaped proximal phalanx of the 2nd toe
HP:0010398	Curved proximal phalanx of the 2nd toe
HP:0010399	Osteolytic defects of the proximal phalanx of the 2nd toe
HP:0010400	Patchy sclerosis of the proximal phalanx of the 2nd toe
HP:0010401	Symphalangism affecting the proximal phalanx of the 2nd toe
HP:0010402	Triangular shaped proximal phalanx of the 2nd toe
HP:0010403	Duplication of the proximal phalanx of the 2nd toe
HP:0010404	Aplasia/Hypoplasia of the middle phalanx of the 2nd toe
HP:0010405	Broad middle phalanx of the 2nd toe
HP:0010406	Bullet-shaped middle phalanx of the 2nd toe
HP:0010407	Curved middle phalanx of the 2nd toe
HP:0010408	Osteolytic defects of the middle phalanx of the 2nd toe
HP:0010409	Patchy sclerosis of the middle phalanx of the 2nd toe
HP:0010410	Symphalangism affecting the middle phalanx of the 2nd toe
HP:0010411	Triangular shaped middle phalanx of the 2nd toe
HP:0010412	Duplication of the middle phalanx of the 2nd toe
HP:0010413	Aplasia/Hypoplasia of the distal phalanx of the 2nd toe
HP:0010414	Broad distal phalanx of the 2nd toe
HP:0010415	Bullet-shaped distal phalanx of the 2nd toe
HP:0010416	Curved distal phalanx of the 2nd toe
HP:0010417	Osteolytic defects of the distal phalanx of the 2nd toe
HP:0010418	Patchy sclerosis of the distal phalanx of the 2nd toe
HP:0010419	Symphalangism affecting the distal phalanx of the 2nd toe
HP:0010420	Triangular shaped distal phalanx of the 2nd toe
HP:0010421	Duplication of the distal phalanx of the 2nd toe
HP:0010422	Complete duplication of the proximal phalanx of the 2nd toe
HP:0010423	Partial duplication of the proximal phalanx of the 2nd toe
HP:0010424	Complete duplication of the distal phalanx of the 2nd toe
HP:0010425	Partial duplication of the distal phalanx of the 2nd toe
HP:0010426	Complete duplication of the middle phalanx of the 2nd toe
HP:0010427	Partial duplication of the middle phalanx of the 2nd toe
HP:0010428	Partial duplication of phalanx of the 2nd toe
HP:0010429	Complete duplication of the phalanges of the 2nd toe
HP:0010430	Aplasia of the phalanges of the 2nd toe
HP:0010431	Short phalanx of the 2nd toe
HP:0010432	Absent distal phalanx of the 2nd toe
HP:0010433	Short distal phalanx of the 2nd toe
HP:0010434	Aplasia of the middle phalanx of the 2nd toe
HP:0010435	Short middle phalanx of the 2nd toe
HP:0010436	Aplasia of the proximal phalanx of the 2nd toe
HP:0010437	Short proximal phalanx of the 2nd toe
HP:0010438	Abnormal ventricular septum morphology
HP:0010440	Ectopic accesory toe-like appendage
HP:0010441	Ectopic accessory finger-like appendage
HP:0010442	Polydactyly
HP:0010443	Bifid femur
HP:0010444	Pulmonary insufficiency
HP:0010445	Primum atrial septal defect
HP:0010446	Tricuspid stenosis
HP:0010447	Anal fistula
HP:0010448	Colonic atresia
HP:0010450	Esophageal stenosis
HP:0010451	Aplasia/Hypoplasia of the spleen
HP:0010452	Ectopia of the spleen
HP:0010453	Pelvic bone asymmetry
HP:0010454	Acetabular spurs
HP:0010455	Steep acetabular roof
HP:0010456	Abnormality of the greater sacrosciatic notch
HP:0010457	Widening of the sacrosciatic notch
HP:0010458	Female pseudohermaphroditism
HP:0010459	True hermaphroditism
HP:0010460	Abnormality of the female genitalia
HP:0010461	Abnormality of the male genitalia
HP:0010462	Aplasia/Hypoplasia of the ovary
HP:0010463	Aplasia of the ovary
HP:0010464	Streak ovary
HP:0010465	Precocious puberty in females
HP:0010468	Aplasia/Hypoplasia of the testes
HP:0010469	Absent testis
HP:0010470	Supernumerary testes
HP:0010471	Oligosacchariduria
HP:0010472	Abnormality of the heme biosynthetic pathway
HP:0010473	Porphyrinuria
HP:0010474	Bladder stones
HP:0010475	Cloacal exstrophy
HP:0010476	Aplasia/Hypoplasia of the bladder
HP:0010477	Aplasia of the bladder
HP:0010478	Abnormality of the urachus
HP:0010479	Patent urachus
HP:0010480	Urethral fistula
HP:0010481	Urethral valve
HP:0010482	Acromelia of the upper limbs
HP:0010483	Amniotic constriction rings of arms
HP:0010484	Hypertrophy of the upper limb
HP:0010485	Hyperextensibility at elbow
HP:0010486	Abnormality of the hypothenar eminence
HP:0010487	Small hypothenar eminence
HP:0010488	Aplasia/Hypoplasia of the palmar creases
HP:0010489	Absent palmar crease
HP:0010490	Abnormality of the palmar creases
HP:0010491	Digital constriction ring
HP:0010492	Osseous finger syndactyly
HP:0010493	Long metacarpals
HP:0010494	Acromelia of the lower limbs
HP:0010495	Amniotic constriction rings of legs
HP:0010496	Hypertrophy of the lower limb
HP:0010497	Sirenomelia
HP:0010498	Bipartite patella
HP:0010499	Patellar subluxation
HP:0010500	Hyperextensibility of the knee
HP:0010501	Limitation of knee mobility
HP:0010502	Fibular bowing
HP:0010503	Fibular duplication
HP:0010504	Increased length of the tibia
HP:0010505	Limitation of movement at ankles
HP:0010506	Abnormal plantar dermatoglyphics
HP:0010507	Foot asymmetry
HP:0010508	Metatarsus valgus
HP:0010509	Aplasia of the tarsal bones
HP:0010510	Hypermobility of toe joints
HP:0010511	Long toe
HP:0010512	Adrenal calcification
HP:0010513	Pituitary calcification
HP:0010514	Hyperpituitarism
HP:0010515	Aplasia/Hypoplasia of the thymus
HP:0010516	Thymus hyperplasia
HP:0010517	Ectopic thymus tissue
HP:0010518	Thyroglossal cyst
HP:0010519	Increased fetal movement
HP:0010521	Gait apraxia
HP:0010522	Dyslexia
HP:0010523	Alexia
HP:0010524	Agnosia
HP:0010525	Finger agnosia
HP:0010526	Dysgraphia
HP:0010527	Astereognosia
HP:0010528	Prosopagnosia
HP:0010529	Echolalia
HP:0010530	Palatal myoclonus
HP:0010531	Spinal myoclonus
HP:0010532	Paroxysmal vertigo
HP:0010533	Spasmus nutans
HP:0010534	Transient global amnesia
HP:0010535	Sleep apnea
HP:0010536	Central sleep apnea
HP:0010537	Wide cranial sutures
HP:0010538	Small sella turcica
HP:0010539	Thin calvarium
HP:0010540	Advanced pneumatization of cranial sinuses
HP:0010541	Cutis gyrata of scalp
HP:0010542	Vestibular nystagmus
HP:0010543	Opsoclonus
HP:0010544	Vertical nystagmus
HP:0010545	Downbeat nystagmus
HP:0010546	Muscle fibrillation
HP:0010547	Muscle flaccidity
HP:0010548	Percussion myotonia
HP:0010549	Weakness due to upper motor neuron dysfunction
HP:0010550	Paraplegia
HP:0010551	Paraplegia/paraparesis
HP:0010553	Oculogyric crisis
HP:0010554	Cutaneous finger syndactyly
HP:0010557	Overlapping fingers
HP:0010558	Abnormality of the clivus
HP:0010559	Vertical clivus
HP:0010560	Undulate clavicles
HP:0010561	Undulate ribs
HP:0010562	Keloids
HP:0010564	Bifid epiglottis
HP:0010565	Aplasia/Hypoplasia of the Epiglottis
HP:0010566	Hamartoma
HP:0010567	Y-shaped metatarsals
HP:0010568	Hamartoma of the eye
HP:0010569	Elevated 7-dehydrocholesterol
HP:0010570	Low maternal serum alpha-fetoprotein
HP:0010571	Elevated levels of phytanic acid
HP:0010574	Abnormality of the epiphysis of the femoral head
HP:0010575	Dysplasia of the femoral head
HP:0010576	Intracranial cystic lesion
HP:0010577	Absent epiphyses
HP:0010578	Bracket epiphyses
HP:0010579	Cone-shaped epiphysis
HP:0010580	Enlarged epiphyses
HP:0010582	Irregular epiphyses
HP:0010583	Ivory epiphyses
HP:0010584	Pseudoepiphyses
HP:0010585	Small epiphyses
HP:0010587	Triangular epiphyses
HP:0010588	Premature epimetaphyseal fusion
HP:0010590	Abnormality of the distal femoral epiphysis
HP:0010591	Abnormality of the proximal tibial epiphysis
HP:0010592	Abnormality of the distal tibial epiphysis
HP:0010593	Abnormality of fibular epiphyses
HP:0010594	Abnormality of the proximal fibular epiphysis
HP:0010595	Abnormality of the distal fibular epiphysis
HP:0010596	Abnormality of the proximal radial epiphysis
HP:0010597	Abnormality of the distal radial epiphysis
HP:0010598	Abnormality of the proximal humeral epiphysis
HP:0010599	Abnormality of the distal humeral epiphysis
HP:0010600	Abnormality of the distal ulnar epiphysis
HP:0010601	Abnormality of the proximal ulnar epiphysis
HP:0010602	Type 2 muscle fiber predominance
HP:0010603	Odontogenic keratocysts of the jaw
HP:0010604	Cyst of the eyelid
HP:0010605	Chalazion
HP:0010606	Hordeolum
HP:0010607	Hordeolum externum
HP:0010608	Hordeolum internum
HP:0010609	Skin tags
HP:0010610	Palmar pits
HP:0010612	Plantar pits
HP:0010614	Fibroma
HP:0010615	Angiofibromas
HP:0010616	Lung fibroma
HP:0010617	Cardiac fibroma
HP:0010618	Ovarian fibroma
HP:0010619	Fibroadenoma of the breast
HP:0010620	Malar prominence
HP:0010621	Cutaneous syndactyly of toes
HP:0010622	Neoplasm of the skeletal system
HP:0010624	Aplastic/hypoplastic toenail
HP:0010625	Anterior pituitary dysgenesis
HP:0010626	Anterior pituitary agenesis
HP:0010627	Anterior pituitary hypoplasia
HP:0010628	Facial palsy
HP:0010629	Abnormal morphology of the cortex of the humerus
HP:0010630	Abnormality of metatarsal epiphysis
HP:0010631	Abnormality of the epiphyses of the feet
HP:0010632	Total anosmia
HP:0010633	Partial anosmia
HP:0010634	Total hyposmia
HP:0010635	Partial hyposmia
HP:0010636	Schizencephaly
HP:0010637	Conjunctival amyloidosis
HP:0010638	Elevated alkaline phosphatase of hepatic origin
HP:0010639	Elevated alkaline phosphatase of bone origin
HP:0010640	Abnormality of the nasal cavity
HP:0010641	Abnormality of the midnasal cavity
HP:0010643	Midnasal atresia
HP:0010644	Midnasal stenosis
HP:0010645	Aplasia of the distal phalanges of the toes
HP:0010646	Cervical spine instability
HP:0010647	Abnormal elasticity of skin
HP:0010648	Dermal translucency
HP:0010649	Flat nasal alae
HP:0010650	Hypoplasia of the premaxilla
HP:0010651	Abnormal meningeal morphology
HP:0010652	Abnormal dura mater morphology
HP:0010653	Abnormality of the falx cerebri
HP:0010654	Aplasia of the falx cerebri
HP:0010655	Epiphyseal stippling
HP:0010656	Abnormal epiphyseal ossification
HP:0010657	Patchy reduction of bone mineral density
HP:0010658	Patchy changes of bone mineral density
HP:0010659	Patchy variation in bone mineral density
HP:0010660	Abnormal hand bone ossification
HP:0010661	Absence of the third cerebral ventricle
HP:0010662	Abnormality of the diencephalon
HP:0010663	Abnormality of thalamus morphology
HP:0010664	Fusion of the left and right thalami
HP:0010665	Bilateral coxa valga
HP:0010666	Hypoplasia of the anterior nasal spine
HP:0010667	Aplasia of the maxilla
HP:0010668	Abnormality of the zygomatic bone
HP:0010669	Hypoplasia of the zygomatic bone
HP:0010672	Abnormality of the third metatarsal bone
HP:0010674	Abnormality of the curvature of the vertebral column
HP:0010675	Abnormal foot bone ossification
HP:0010676	Mechanical ileus
HP:0010677	Enuresis nocturna
HP:0010678	Enuresis diurna
HP:0010679	Elevated tissue non-specific alkaline phosphatase
HP:0010680	Elevated alkaline phosphatase of renal origin
HP:0010681	Elevated intestinal alkaline phosphatase
HP:0010682	Elevated placental alkaline phosphatase
HP:0010683	Low tissue non-specific alkaline phosphatase
HP:0010684	Low alkaline phosphatase of bone origin
HP:0010685	Low alkaline phosphatase of renal origin
HP:0010686	Low alkaline phosphatase of hepatic origin
HP:0010687	Low intestinal alkaline phosphatase
HP:0010688	Low placental alkaline phosphatase
HP:0010689	Mirror image polydactyly
HP:0010690	Mirror image hand polydactyly
HP:0010691	Mirror image foot polydactyly
HP:0010692	2-5 finger syndactyly
HP:0010693	Pulverulent cataract
HP:0010694	Lamellar pulverulent cataract
HP:0010695	Sutural cataract
HP:0010696	Polar cataract
HP:0010697	Anterior pyramidal cataract
HP:0010698	Nuclear pulverulent cataract
HP:0010699	Triangular nuclear cataract
HP:0010700	obsolete Total cataract
HP:0010701	Abnormal immunoglobulin level
HP:0010702	Increased antibody level in blood
HP:0010704	1-2 finger syndactyly
HP:0010705	4-5 finger syndactyly
HP:0010706	1-3 finger syndactyly
HP:0010707	1-4 finger syndactyly
HP:0010708	1-5 finger syndactyly
HP:0010709	2-4 finger syndactyly
HP:0010710	3-5 finger syndactyly
HP:0010711	1-2 toe syndactyly
HP:0010712	1-4 toe syndactyly
HP:0010713	1-5 toe syndactyly
HP:0010714	2-4 toe syndactyly
HP:0010715	2-5 toe syndactyly
HP:0010716	3-5 toe syndactyly
HP:0010717	Osseous syndactyly of toes
HP:0010719	Abnormality of hair texture
HP:0010720	Abnormal hair pattern
HP:0010721	Abnormal hair whorl
HP:0010722	Asymmetry of the ears
HP:0010723	Cystic lesions of the pinnae
HP:0010724	Advanced pneumatization of the mastoid process
HP:0010726	Prominent corneal nerve fibers
HP:0010727	Spontaneous rupture of the globe
HP:0010728	Aplasia of the retina
HP:0010729	Cherry red spot of the macula
HP:0010730	Double eyebrow
HP:0010731	Extension of eyebrows towards upper eyelid
HP:0010732	Nodular changes affecting the eyelids
HP:0010733	Naevus flammeus of the eyelid
HP:0010734	Fibrous dysplasia of the bones
HP:0010735	Polyostotic fibrous dysplasia
HP:0010736	Monostotic fibrous dysplasia
HP:0010739	Osteopoikilosis
HP:0010740	Osteopathia striata
HP:0010741	Edema of the lower limbs
HP:0010742	Edema of the upper limbs
HP:0010743	Short metatarsal
HP:0010744	Absent metatarsal bone
HP:0010745	Aplasia of the phalanges of the toes
HP:0010746	Hypoplasia of the phalanges of the toes
HP:0010747	Medial flaring of the eyebrow
HP:0010748	Ectopic lacrimal punctum
HP:0010749	Blepharochalasis
HP:0010750	Dermatochalasis
HP:0010751	Dimple chin
HP:0010752	Cleft mandible
HP:0010753	Midline defect of mandible
HP:0010754	Abnormality of the temporomandibular joint
HP:0010755	Asymmetry of the maxilla
HP:0010756	Aplasia/Hypoplasia of the premaxilla
HP:0010757	Aplasia of the premaxilla
HP:0010758	Abnormality of the premaxilla
HP:0010759	Prominence of the premaxilla
HP:0010760	Absent toe
HP:0010761	Broad columella
HP:0010762	Chordoma
HP:0010763	Low insertion of columella
HP:0010764	Short eyelashes
HP:0010765	Palmar hyperkeratosis
HP:0010766	Ectopic calcification
HP:0010767	Sacrococcygeal pilonidal abnormality
HP:0010769	Pilonidal sinus
HP:0010770	Pilonidal fistula
HP:0010771	Pilonidal abscess
HP:0010772	Anomalous pulmonary venous return
HP:0010773	Partial anomalous pulmonary venous return
HP:0010774	Cor triatriatum
HP:0010775	Vascular ring
HP:0010776	Tracheobronchmegaly
HP:0010777	Bronchomegaly
HP:0010778	Tracheomegaly
HP:0010779	Large pelvis bone
HP:0010780	Hyperacusis
HP:0010781	Skin dimples
HP:0010782	Shoulder dimples
HP:0010783	Erythema
HP:0010784	Uterine neoplasm
HP:0010785	Gonadal neoplasm
HP:0010786	Urinary tract neoplasm
HP:0010787	Genital neoplasm
HP:0010788	Testicular neoplasm
HP:0010789	Abnormality of the Leydig cells
HP:0010790	Hyoplasia of the Leydig cells
HP:0010791	Hyperplasia of the Leydig cells
HP:0010793	Bifid nail
HP:0010794	Impaired visuospatial constructive cognition
HP:0010795	Cerebellar glioma
HP:0010796	Brainstem glioma
HP:0010797	Hemangioblastoma
HP:0010798	Lip freckle
HP:0010799	Pinealoma
HP:0010800	Absent cupid's bow
HP:0010801	Underdeveloped nasolabial fold
HP:0010802	Perioral hyperpigmentation
HP:0010803	Everted upper lip vermilion
HP:0010804	Tented upper lip vermilion
HP:0010805	Upturned corners of mouth
HP:0010806	U-Shaped upper lip vermilion
HP:0010807	Open bite
HP:0010808	Protruding tongue
HP:0010809	Broad uvula
HP:0010810	Long uvula
HP:0010811	Narrow uvula
HP:0010812	Short uvula
HP:0010813	Abnormal number of hair whorls
HP:0010814	Abnormal position of hair whorl
HP:0010815	Nevus sebaceous
HP:0010816	Epidermal nevus
HP:0010817	Linear nevus sebaceous
HP:0010818	Generalized tonic seizures
HP:0010819	Atonic seizures
HP:0010820	Dacrystic seizures
HP:0010821	Gelastic seizures
HP:0010822	Scintillating scotoma
HP:0010823	Ridged cranial sutures
HP:0010824	Abnormal fifth cranial nerve morphology
HP:0010825	Abnormality of the eleventh cranial nerve
HP:0010826	Abnormality of the twelfth cranial nerve
HP:0010827	Abnormality of the seventh cranial nerve
HP:0010828	Hemifacial spasm
HP:0010829	Impaired temperature sensation
HP:0010830	Impaired tactile sensation
HP:0010831	Impaired proprioception
HP:0010832	Abnormality of pain sensation
HP:0010833	Spontaneous pain sensation
HP:0010834	Trophic changes related to pain
HP:0010835	Dissociated sensory loss
HP:0010836	Abnormality of copper homeostasis
HP:0010837	Decreased serum ceruloplasmin
HP:0010838	High nonceruloplasmin-bound serum copper
HP:0010839	Increased urinary copper concentration
HP:0010841	Multifocal epileptiform discharges
HP:0010843	EEG with focal slow activity
HP:0010844	EEG with multifocal slow activity
HP:0010845	EEG with generalized slow activity
HP:0010846	EEG with persistent abnormal rhythmic activity
HP:0010847	EEG with spike-wave complexes (<2.5 Hz)
HP:0010848	EEG with spike-wave complexes (2.5-3.5 Hz)
HP:0010849	EEG with spike-wave complexes (>3.5 Hz)
HP:0010850	EEG with spike-wave complexes
HP:0010851	EEG with burst suppression
HP:0010852	EEG with photoparoxysmal response
HP:0010853	EEG with periodic lateralized epileptiform discharges
HP:0010854	EEG with generalized low amplitude activity
HP:0010855	EEG with localized low amplitude activity
HP:0010856	EEG with periodic complexes
HP:0010857	EEG with periodic abnormalities
HP:0010858	EEG with hyperventilation-induced epileptiform discharges
HP:0010859	Frank breech presentation
HP:0010860	Complete breech presentation
HP:0010861	Incomplete breech presentation
HP:0010862	Delayed fine motor development
HP:0010863	Receptive language delay
HP:0010864	Intellectual disability, severe
HP:0010865	Oppositional defiant disorder
HP:0010866	Abdominal wall defect
HP:0010867	Dyssynergia
HP:0010868	Ocular dyssynergia
HP:0010869	Asynergia
HP:0010871	Sensory ataxia
HP:0010872	T-wave inversion
HP:0010873	Cervical spinal cord atrophy
HP:0010874	Tendon xanthomatosis
HP:0010875	Chaddock reflex
HP:0010876	Abnormality of circulating protein level
HP:0010877	Monocular strabismus
HP:0010878	Fetal cystic hygroma
HP:0010879	Postnatal cystic hygroma
HP:0010880	Increased nuchal translucency
HP:0010881	Abnormality of the umbilical cord
HP:0010882	Pulmonary valve atresia
HP:0010883	Aortic valve atresia
HP:0010884	Acromelia
HP:0010885	Aseptic necrosis
HP:0010886	Osteochondritis Dissecans
HP:0010888	Morbus Koehler
HP:0010889	Morbus Kienboeck
HP:0010890	Morbus Osgood-Schlatter
HP:0010891	Morbus Scheuermann
HP:0010892	Abnormality of branched chain family amino acid metabolism
HP:0010893	Abnormality of phenylalanine metabolism
HP:0010894	Abnormality of serine family amino acid metabolism
HP:0010895	Abnormality of glycine metabolism
HP:0010896	Hypersarcosinemia
HP:0010897	Hypersarcosinuria
HP:0010898	Abnormality of sarcosine metabolism
HP:0010899	Abnormality of aspartate family amino acid metabolism
HP:0010900	Abnormality of threonine metabolism
HP:0010901	Abnormality of methionine metabolism
HP:0010902	Abnormality of glutamine family amino acid metabolism
HP:0010903	Abnormality of glutamine metabolism
HP:0010904	Abnormality of histidine metabolism
HP:0010905	obsolete Abnormality of histidine metabolism
HP:0010906	Hyperhistidinemia
HP:0010907	Abnormality of proline metabolism
HP:0010908	Abnormality of lysine metabolism
HP:0010909	Abnormality of arginine metabolism
HP:0010910	Hypervalinemia
HP:0010911	Hyperleucinemia
HP:0010912	Abnormality of isoleucine metabolism
HP:0010913	Hyperisoleucinemia
HP:0010914	Abnormality of valine metabolism
HP:0010915	Abnormal circulating pyruvate family amino acid concentration
HP:0010916	Abnormal circulating alanine concentration
HP:0010917	Abnormality of tyrosine metabolism
HP:0010918	Abnormality of cysteine metabolism
HP:0010919	Abnormality of homocysteine metabolism
HP:0010920	Zonular cataract
HP:0010921	Coralliform cataract
HP:0010922	Membranous cataract
HP:0010923	Anterior subcapsular cataract
HP:0010924	Posterior cortical cataract
HP:0010925	Nuclear punctate cataract
HP:0010926	Aculeiform cataract
HP:0010927	Abnormality of divalent inorganic cation homeostasis
HP:0010928	Abnormality of orotic acid metabolism
HP:0010929	Abnormality of cation homeostasis
HP:0010930	Abnormality of monovalent inorganic cation homeostasis
HP:0010931	Abnormality of sodium homeostasis
HP:0010932	Abnormality of nucleobase metabolism
HP:0010933	Abnormality of xanthine metabolism
HP:0010934	Xanthinuria
HP:0010935	Abnormality of the upper urinary tract
HP:0010936	Abnormality of the lower urinary tract
HP:0010937	Abnormality of the nasal skeleton
HP:0010938	Abnormality of the external nose
HP:0010939	Abnormality of the nasal bone
HP:0010940	Aplasia/Hypoplasia of the nasal bone
HP:0010941	Aplasia of the nasal bone
HP:0010942	Echogenic intracardiac focus
HP:0010943	Echogenic fetal bowel
HP:0010944	Abnormality of the renal pelvis
HP:0010945	Fetal pyelectasis
HP:0010946	Dilatation of the renal pelvis
HP:0010947	Abnormality of ductus venosus blood flow
HP:0010948	Abnormality of the fetal cardiovascular system
HP:0010949	Abnormality of umbilical vein blood flow
HP:0010950	Abnormality of the fourth ventricle
HP:0010951	Abnormality of the third ventricle
HP:0010952	Mild fetal ventriculomegaly
HP:0010953	Noncommunicating hydrocephalus
HP:0010954	Hypoplastic right heart
HP:0010955	Dilatation of the bladder
HP:0010956	Fetal megacystis
HP:0010957	Congenital posterior urethral valve
HP:0010958	Bilateral renal agenesis
HP:0010959	Congenital cystic adenomatoid malformation of the lung
HP:0010960	Bronchopulmonary sequestration
HP:0010961	Intralobar sequestration
HP:0010962	Extralobar sequestration
HP:0010963	Absence of stomach bubble on fetal sonography
HP:0010964	Abnormality of long-chain fatty-acid metabolism
HP:0010965	Abnormality of phytanic acid metabolism
HP:0010966	Abnormality of fatty-acid anion metabolism
HP:0010967	Abnormality of carnitine metabolism
HP:0010968	Abnormality of liposaccharide metabolism
HP:0010969	Abnormality of glycolipid metabolism
HP:0010970	Blood group antigen abnormality
HP:0010971	Absence of Lutheran antigen on erythrocytes
HP:0010972	Anemia of inadequate production
HP:0010974	Abnormality of myeloid leukocytes
HP:0010975	Abnormal B cell count
HP:0010976	B lymphocytopenia
HP:0010977	Abnormality of phagocytes
HP:0010978	Abnormality of immune system physiology
HP:0010979	Abnormality of lipoprotein cholesterol concentration
HP:0010980	Hyperlipoproteinemia
HP:0010981	Hypolipoproteinemia
HP:0010982	Polygenic inheritance
HP:0010983	Oligogenic inheritance
HP:0010984	Digenic inheritance
HP:0010985	Gonosomal inheritance
HP:0010987	Abnormality of cellular immune system
HP:0010988	Abnormality of the extrinsic pathway
HP:0010989	Abnormality of the intrinsic pathway
HP:0010990	Abnormality of the common coagulation pathway
HP:0010991	Abnormality of the abdominal musculature
HP:0010992	Stress urinary incontinence
HP:0010993	Abnormality of the cerebral subcortex
HP:0010994	Abnormal corpus striatum morphology
HP:0010995	Abnormality of dicarboxylic acid metabolism
HP:0010996	Abnormality of monocarboxylic acid metabolism
HP:0010997	Chromosomal breakage induced by ionizing radiation
HP:0010998	Increased susceptibility to spontaneous sister chromatid exchange
HP:0010999	Aplasia of the optic tract
HP:0011000	Aplasia/Hypoplasia of the optic tract
HP:0011001	Increased bone mineral density
HP:0011002	Osteopetrosis
HP:0011003	High myopia
HP:0011004	Abnormal systemic arterial morphology
HP:0011005	Mixed cirrhosis
HP:0011006	Abnormality of the musculature of the neck
HP:0011008	Temporal pattern
HP:0011009	Acute
HP:0011010	Chronic
HP:0011011	Subacute
HP:0011012	Abnormality of polysaccharide metabolism
HP:0011013	Abnormality of carbohydrate metabolism/homeostasis
HP:0011014	Abnormal glucose homeostasis
HP:0011015	Abnormality of blood glucose concentration
HP:0011016	Abnormality of urine glucose concentration
HP:0011017	Abnormal cellular physiology
HP:0011018	Abnormality of the cell cycle
HP:0011019	Abnormality of chromosome condensation
HP:0011020	Abnormality of mucopolysaccharide metabolism
HP:0011021	Abnormality of circulating enzyme level
HP:0011022	Abnormality of unsaturated fatty acid metabolism
HP:0011023	Abnormality of prostaglandin metabolism
HP:0011024	Abnormality of the gastrointestinal tract
HP:0011025	Abnormal cardiovascular system physiology
HP:0011026	Aplasia/Hypoplasia of the vagina
HP:0011027	Abnormality of the fallopian tube
HP:0011028	Abnormality of blood circulation
HP:0011029	Internal hemorrhage
HP:0011030	Abnormality of transition element cation homeostasis
HP:0011031	Abnormality of iron homeostasis
HP:0011032	Abnormality of fluid regulation
HP:0011033	Impairment of fructose metabolism
HP:0011034	Amyloidosis
HP:0011035	Abnormality of renal cortex morphology
HP:0011036	Abnormality of renal excretion
HP:0011037	Decreased urine output
HP:0011038	Abnormality of renal resorption
HP:0011039	Abnormality of the helix
HP:0011040	Abnormality of the intrahepatic bile duct
HP:0011041	Aplasia/Hypoplasia of the cervical spine
HP:0011042	Abnormality of potassium homeostasis
HP:0011043	Abnormality of circulating adrenocorticotropin level
HP:0011044	Abnormal number of permanent teeth
HP:0011045	Agenesis of permanent maxillary central incisor
HP:0011046	Agenesis of primary maxillary central incisor
HP:0011047	Agenesis of primary mandibular central incisor
HP:0011048	Agenesis of permanent mandibular central incisor
HP:0011049	Agenesis of primary maxillary lateral incisor
HP:0011050	Agenesis of permanent maxillary lateral incisor
HP:0011051	Agenesis of premolar
HP:0011052	Agenesis of maxillary premolar
HP:0011053	Agenesis of mandibular premolar
HP:0011054	Agenesis of molar
HP:0011055	Agenesis of permanent molar
HP:0011056	Agenesis of first permanent molar tooth
HP:0011057	Agenesis of second permanent molar
HP:0011058	Generalized periodontitis
HP:0011059	Localized periodontitis
HP:0011060	Dentinogenesis imperfecta limited to primary teeth
HP:0011061	Abnormality of dental structure
HP:0011062	Misalignment of incisors
HP:0011063	Abnormality of incisor morphology
HP:0011064	Abnormal number of incisors
HP:0011065	Conical incisor
HP:0011067	Mesiodens
HP:0011068	Odontoma
HP:0011069	Increased number of teeth
HP:0011070	Abnormality of molar morphology
HP:0011071	Abnormality of permanent molar morphology
HP:0011072	Rootless teeth
HP:0011073	Abnormality of dental color
HP:0011074	Localized hypoplasia of dental enamel
HP:0011075	Green teeth
HP:0011076	Abnormality of premolar
HP:0011077	Abnormality of molar
HP:0011078	Abnormality of canine
HP:0011079	Impacted tooth
HP:0011080	Abnormality of premolar morphology
HP:0011081	Incisor macrodontia
HP:0011082	Conical primary incisor
HP:0011083	Conical maxillary incisor
HP:0011084	Hypocalcification of dental enamel
HP:0011085	Hypomature dental enamel
HP:0011086	Dentinogenesis imperfecta of primary and permanent teeth
HP:0011087	Talon cusp
HP:0011088	Dens in dente
HP:0011089	Double tooth
HP:0011090	Fused teeth
HP:0011091	Gemination
HP:0011092	Mulberry molar
HP:0011093	Molarization of premolar
HP:0011094	Overbite
HP:0011095	Overjet
HP:0011096	Peripheral demyelination
HP:0011097	Epileptic spasms
HP:0011098	Speech apraxia
HP:0011099	Spastic hemiparesis
HP:0011100	Intestinal atresia
HP:0011102	Ileal atresia
HP:0011103	Abnormal left ventricular outflow tract morphology
HP:0011104	Abnormality of blood volume homeostasis
HP:0011105	Hypervolemia
HP:0011106	Hypovolemia
HP:0011107	Recurrent aphthous stomatitis
HP:0011108	Recurrent sinusitis
HP:0011109	Chronic sinusitis
HP:0011110	Tonsillitis
HP:0011111	Abnormality of immune serum protein physiology
HP:0011112	Abnormality of serum cytokine level
HP:0011113	Abnormality of cytokine secretion
HP:0011114	Defective production of NFKB1-dependent cytokines
HP:0011115	Abnormality of chemokine secretion
HP:0011116	Abnormality of interferon secretion
HP:0011117	Abnormality of interleukin secretion
HP:0011118	Abnormality of tumor necrosis factor secretion
HP:0011119	Abnormality of the nasal dorsum
HP:0011120	Concave nasal ridge
HP:0011121	Abnormality of skin morphology
HP:0011122	Abnormality of skin physiology
HP:0011123	Inflammatory abnormality of the skin
HP:0011124	Abnormality of epidermal morphology
HP:0011125	Abnormality of dermal melanosomes
HP:0011126	Nephroptosis
HP:0011127	Perioral eczema
HP:0011128	Acute esophageal necrosis
HP:0011129	Bilateral fetal pyelectasis
HP:0011130	Abnormality of renal calyx morphology
HP:0011131	Perianal rash
HP:0011132	Chronic furunculosis
HP:0011133	Increased sensitivity to ionizing radiation
HP:0011134	Low-grade fever
HP:0011135	Aplasia/Hypoplasia of the sweat glands
HP:0011136	Aplasia of the sweat glands
HP:0011137	Non-pruritic urticaria
HP:0011138	Abnormality of skin adnexa morphology
HP:0011139	Gastric duplication
HP:0011140	Gastrointestinal duplication
HP:0011141	Age-related cataract
HP:0011142	Age-related nuclear cataract
HP:0011143	Age-related cortical cataract
HP:0011144	Age-related posterior subcapsular cataract
HP:0011145	Symptomatic seizures
HP:0011146	obsolete Dialeptic seizures
HP:0011147	Typical absence seizure
HP:0011148	obsolete Absence seizures with special features
HP:0011149	Absence seizure with eyelid myoclonia
HP:0011150	Myoclonic absence
HP:0011151	Obtundation status
HP:0011152	Early onset absence seizures
HP:0011153	Focal motor seizure
HP:0011154	Focal autonomic seizure
HP:0011155	Focal autonomic seizures with altered responsiveness
HP:0011156	Focal autonomic seizures without altered responsiveness
HP:0011157	Focal sensory seizure
HP:0011158	Focal sensory auditory seizure
HP:0011159	Epigastric auras
HP:0011160	Focal sensory gustatory seizure
HP:0011161	Olfactory auras
HP:0011162	Psychic auras
HP:0011163	Somatosensory auras
HP:0011164	Vegetative auras
HP:0011165	Visual auras
HP:0011166	Focal myoclonic seizures
HP:0011167	Focal tonic seizures
HP:0011168	Eyelid myoclonias
HP:0011169	Generalized clonic seizures
HP:0011170	Myoclonic atonic seizures
HP:0011171	Simple febrile seizures
HP:0011172	Complex febrile seizures
HP:0011173	Hypokinetic seizures
HP:0011174	Hyperkinetic seizures
HP:0011175	Versive seizures
HP:0011176	EEG with constitutional variants
HP:0011177	EEG with 4-5/second background activity
HP:0011178	Alpha-EEG
HP:0011179	Beta-EEG
HP:0011180	Partial beta-EEG
HP:0011181	Low voltage EEG
HP:0011182	Interictal epileptiform activity
HP:0011183	EEG with hyperventilation-induced focal epileptiform discharges
HP:0011184	EEG with hyperventilation-induced generalized epileptiform discharges
HP:0011185	EEG with focal epileptiform discharges
HP:0011186	Focal epileptiform discharges with limited propagation to contralateral hemisphere
HP:0011187	Focal EEG discharges with propagation to ipsilateral hemisphere
HP:0011188	Focal EEG discharges with secondary generalization
HP:0011189	Bilateral multifocal epileptiform discharges
HP:0011190	Uni- and bilateral multifocal epileptiform discharges
HP:0011191	Unilateral multifocal epileptiform discharges
HP:0011192	Polymorphic focal epileptiform discharges
HP:0011193	EEG with focal spikes
HP:0011194	EEG with series of focal spikes
HP:0011195	EEG with focal sharp slow waves
HP:0011196	EEG with focal sharp waves
HP:0011197	EEG with focal spike waves
HP:0011198	EEG with generalized epileptiform discharges
HP:0011199	EEG with generalized sharp slow waves
HP:0011200	EEG with generalized polymorphic epileptiform discharges
HP:0011201	EEG with changes in voltage
HP:0011202	EEG with diffuse acceleration
HP:0011203	EEG with abnormally slow frequencies
HP:0011204	EEG with continuous slow activity
HP:0011205	EEG with intermittent slow activity
HP:0011206	EEG with generalized slow activity grade 1
HP:0011207	EEG with generalized slow activity grade 2
HP:0011208	EEG with generalized slow activity grade 3
HP:0011209	EEG with generalized slow activity grade 4
HP:0011210	EEG with occipital slowing
HP:0011211	EEG with photoparoxysmal response grade I
HP:0011212	EEG with photoparoxysmal response grade II
HP:0011213	EEG with photoparoxysmal response grade III
HP:0011214	EEG with photoparoxysmal response grade IV
HP:0011215	Hemihypsarrhythmia
HP:0011217	Abnormal shape of the occiput
HP:0011218	Abnormal shape of the frontal region
HP:0011219	Short face
HP:0011220	Prominent forehead
HP:0011221	Vertical forehead creases
HP:0011222	Depressed glabella
HP:0011223	Metopic depression
HP:0011224	Ablepharon
HP:0011225	Epiblepharon
HP:0011226	Aplasia/Hypoplasia of the eyelid
HP:0011227	Elevated C-reactive protein level
HP:0011228	Horizontal eyebrow
HP:0011229	Broad eyebrow
HP:0011230	Laterally extended eyebrow
HP:0011231	Prominent eyelashes
HP:0011232	Infra-orbital fold
HP:0011233	Antihelical shelf
HP:0011234	Absent antihelix
HP:0011235	Additional crus of antihelix
HP:0011236	Angulated antihelix
HP:0011237	Broad inferior crus of antihelix
HP:0011238	Prominent inferior crus of antihelix
HP:0011239	Underdeveloped inferior crus of antihelix
HP:0011240	Prominent stem of antihelix
HP:0011241	Serpiginous stem of antihelix
HP:0011242	Underdeveloped stem of antihelix
HP:0011243	Abnormality of inferior crus of antihelix
HP:0011244	Abnormality of stem of antihelix
HP:0011245	Abnormality of superior crus of antihelix
HP:0011246	Underdeveloped superior crus of antihelix
HP:0011247	Prominent superior crus of antihelix
HP:0011248	Everted antitragus
HP:0011249	Absent antitragus
HP:0011250	Bifid antitragus
HP:0011251	Underdeveloped antitragus
HP:0011252	Cryptotia
HP:0011253	Type I cryptotia
HP:0011254	Type II cryptotia
HP:0011255	Absent crus of helix
HP:0011256	Crus of helix connected to antihelix
HP:0011257	Serpiginous crus of helix
HP:0011258	Tragal bridge of crus of helix
HP:0011259	Expanded terminal portion of crus of helix
HP:0011260	Darwin notch of helix
HP:0011261	Darwin tubercle of helix
HP:0011262	Crimped helix
HP:0011263	Forward facing earlobe
HP:0011264	Discontinuous ascending root of helix
HP:0011265	Cleft earlobe
HP:0011266	Microtia, first degree
HP:0011267	Microtia, third degree
HP:0011268	Absent tragus
HP:0011269	Bifid tragus
HP:0011270	Duplicated tragus
HP:0011271	Prominent tragus
HP:0011272	Underdeveloped tragus
HP:0011273	Anisocytosis
HP:0011274	Recurrent mycobacterial infections
HP:0011275	Recurrent mycobacterium avium complex infections
HP:0011276	Vascular skin abnormality
HP:0011277	Abnormality of the urinary system physiology
HP:0011278	Intrapulmonary sequestration
HP:0011279	Abnormality of urine bicarbonate concentration
HP:0011280	Abnormality of urine calcium concentration
HP:0011281	Abnormality of urine catecholamine concentration
HP:0011282	Abnormality of hindbrain morphology
HP:0011283	Abnormality of the metencephalon
HP:0011284	Short-segment aganglionic megacolon
HP:0011285	Long-segment aganglionic megacolon
HP:0011286	Total colonic aganglionosis
HP:0011287	EEG with occipital sharp slow waves
HP:0011288	EEG with parietal sharp slow waves
HP:0011289	EEG with temporal sharp slow waves
HP:0011290	EEG with frontal sharp slow waves
HP:0011291	EEG with central sharp slow waves
HP:0011292	EEG with occipital sharp waves
HP:0011293	EEG with central sharp waves
HP:0011294	EEG with frontal sharp waves
HP:0011295	EEG with parietal sharp waves
HP:0011296	EEG with temporal sharp waves
HP:0011297	Abnormality of digit
HP:0011298	Prominent digit pad
HP:0011299	Partial absence of finger
HP:0011300	Broad fingertip
HP:0011301	Absent foot
HP:0011302	Long palm
HP:0011303	Convex contour of sole
HP:0011304	Broad thumb
HP:0011305	Partial absence of toe
HP:0011307	Splayed toes
HP:0011308	Slender toe
HP:0011309	Tapered toe
HP:0011310	Bridged palmar crease
HP:0011311	Sydney crease
HP:0011312	Fused nails
HP:0011313	Narrow nail
HP:0011314	Abnormality of long bone morphology
HP:0011315	Unicoronal synostosis
HP:0011316	Left unicoronal synostosis
HP:0011317	Right unicoronal synostosis
HP:0011318	Bicoronal synostosis
HP:0011319	Bilambdoid synostosis
HP:0011320	Unilambdoid synostosis
HP:0011321	Left unilambdoid synostosis
HP:0011322	Right unilambdoid synostosis
HP:0011323	Cleft of chin
HP:0011324	Multiple suture craniosynostosis
HP:0011325	Pansynostosis
HP:0011326	Anterior plagiocephaly
HP:0011327	Posterior plagiocephaly
HP:0011328	Abnormality of fontanelles
HP:0011329	Abnormality of cranial sutures
HP:0011330	Metopic synostosis
HP:0011331	Hemifacial atrophy
HP:0011332	Hemifacial hypoplasia
HP:0011333	Asymmetric crying face
HP:0011334	Facial shape deformation
HP:0011335	Frontal hirsutism
HP:0011336	Bitemporal forceps marks
HP:0011337	Abnormality of mouth size
HP:0011338	Abnormality of mouth shape
HP:0011339	Abnormality of upper lip vermillion
HP:0011340	Incomplete cleft of the upper lip
HP:0011341	Long upper lip
HP:0011342	Mild global developmental delay
HP:0011343	Moderate global developmental delay
HP:0011344	Severe global developmental delay
HP:0011345	Moderate expressive language delay
HP:0011346	Mild expressive language delay
HP:0011347	Abnormality of ocular abduction
HP:0011348	Abnormality of the sixth cranial nerve
HP:0011349	Abducens palsy
HP:0011350	Mild receptive language delay
HP:0011351	Moderate receptive language delay
HP:0011352	Severe receptive language delay
HP:0011353	Arterial intimal fibrosis
HP:0011354	Generalized abnormality of skin
HP:0011355	Localized skin lesion
HP:0011356	Regional abnormality of skin
HP:0011357	Abnormality of hair density
HP:0011358	Generalized hypopigmentation of hair
HP:0011359	Dry hair
HP:0011360	Acquired abnormal hair pattern
HP:0011361	Congenital abnormal hair pattern
HP:0011362	Abnormal hair quantity
HP:0011363	Abnormality of hair growth rate
HP:0011364	White hair
HP:0011365	Patchy hypopigmentation of hair
HP:0011367	Yellow nails
HP:0011368	Epidermal thickening
HP:0011369	Mongolian blue spot
HP:0011370	Recurrent cutaneous fungal infections
HP:0011371	Recurrent viral skin infections
HP:0011372	Aplasia of the inner ear
HP:0011373	Incomplete partition of the cochlea
HP:0011374	Incomplete partition of the cochlea type I
HP:0011375	Cochlear aplasia
HP:0011376	Morphological abnormality of the vestibule of the inner ear
HP:0011377	Aplasia of the vestibule
HP:0011378	Hypoplasia of the vestibule of the inner ear
HP:0011379	Dilated vestibule of the inner ear
HP:0011380	Morphological abnormality of the semicircular canal
HP:0011381	Aplasia of the semicircular canal
HP:0011382	Hypoplasia of the semicircular canal
HP:0011383	Enlarged semicircular canal
HP:0011384	Abnormality of the internal auditory canal
HP:0011385	Absent internal auditory canal
HP:0011386	Narrow internal auditory canal
HP:0011387	Enlarged vestibular aqueduct
HP:0011388	Enlarged cochlear aqueduct
HP:0011389	Functional abnormality of the inner ear
HP:0011390	Morphological abnormality of the inner ear
HP:0011391	Morphological abnormality of the nerves of the inner ear
HP:0011392	Abnormality of the vestibular nerve
HP:0011393	Aplasia of the vestibular nerve.
HP:0011394	Hypoplasia of the vestibular nerve
HP:0011395	Aplasia/Hypoplasia of the cochlea
HP:0011396	Abnormality of the cochlear nerve
HP:0011397	Abnormality of the dorsal column of the spinal cord
HP:0011398	Central hypotonia
HP:0011399	Tibialis atrophy
HP:0011400	Abnormal CNS myelination
HP:0011401	Delayed peripheral myelination
HP:0011402	Demyelinating sensory neuropathy
HP:0011403	Abnormal umbilical cord blood vessels
HP:0011404	Lethal short-trunk short stature
HP:0011405	Childhood onset short-limb short stature
HP:0011406	Infancy onset short-trunk short stature
HP:0011407	Proportionate tall stature
HP:0011408	Moderate intrauterine growth retardation
HP:0011409	Abnormality of placental membranes
HP:0011410	Caesarian section
HP:0011411	Forceps delivery
HP:0011412	Ventouse delivery
HP:0011413	Shoulder dystocia
HP:0011414	Hydropic placenta
HP:0011415	Calcified placenta
HP:0011416	Placental infarction
HP:0011417	Long umbilical cord
HP:0011418	Abnormal insertion of umbilical cord
HP:0011419	Placental abruption
HP:0011420	Age of death
HP:0011421	Death in adolescence
HP:0011422	Abnormality of chloride homeostasis
HP:0011423	Hyperchloremia
HP:0011424	Increased serum zinc
HP:0011425	Fetal ultrasound soft marker
HP:0011426	Fetal choroid plexus cysts
HP:0011427	Enlarged fetal cisterna magna
HP:0011428	Short fetal femur length
HP:0011429	Short fetal humerus length
HP:0011430	Hypoplasia of fetal nasal bone
HP:0011431	Fetal fifth finger clinodactyly
HP:0011432	High maternal serum alpha-fetoprotein
HP:0011433	High maternal serum chorionic gonadotropin
HP:0011434	Low maternal serum chorionic gonadotropin
HP:0011435	Low maternal serum PAPP-A
HP:0011436	Abnormal maternal serum screening
HP:0011437	Maternal autoimmune disease
HP:0011438	Maternal teratogenic exposure
HP:0011439	Anesthetic-induced rhabdomylosis
HP:0011440	Alcohol-induced rhabdomyolysis
HP:0011441	Abnormality of the medulla oblongata
HP:0011442	Abnormality of central motor function
HP:0011443	Abnormality of coordination
HP:0011444	Decorticate rigidity
HP:0011445	Athetoid cerebral palsy
HP:0011446	Abnormality of higher mental function
HP:0011447	Hyposegmentation of neutrophil nuclei
HP:0011448	Ankle clonus
HP:0011449	Knee clonus
HP:0011450	Unusual CNS infection
HP:0011451	Congenital microcephaly
HP:0011452	Functional abnormality of the middle ear
HP:0011453	Abnormality of the incus
HP:0011454	Abnormality of the malleus
HP:0011455	Absent malleus
HP:0011456	Absent stapes
HP:0011457	Loss of eyelashes
HP:0011458	Abdominal symptom
HP:0011459	Esophageal carcinoma
HP:0011460	Embryonal onset
HP:0011461	Fetal onset
HP:0011462	Young adult onset
HP:0011463	Childhood onset
HP:0011464	Aganglionosis of the small intestine
HP:0011465	Duodenal aganglionosis
HP:0011466	Aplasia/Hypoplasia of the gallbladder
HP:0011467	Absent gallbladder
HP:0011468	Facial tics
HP:0011469	Nasal regurgitation
HP:0011470	Nasogastric tube feeding in infancy
HP:0011471	Gastrostomy tube feeding in infancy
HP:0011472	Abnormality of small intestinal villus morphology
HP:0011473	Villous atrophy
HP:0011474	Childhood onset sensorineural hearing impairment
HP:0011475	Persistent stapedial artery
HP:0011476	Profound sensorineural hearing impairment
HP:0011477	Upbeat nystagmus
HP:0011478	True anophthalmia
HP:0011479	Abnormal lacrimal punctum morphology
HP:0011480	Unilateral microphthalmos
HP:0011481	Abnormal lacrimal duct morphology
HP:0011482	Abnormal lacrimal gland morphology
HP:0011483	Anterior synechiae of the anterior chamber
HP:0011484	Posterior synechiae of the anterior chamber
HP:0011485	Corneolenticular adhesion
HP:0011486	Abnormality of corneal thickness
HP:0011487	Increased corneal thickness
HP:0011488	Abnormal corneal endothelium morphology
HP:0011489	Abnormal migration of corneal endothelium
HP:0011490	Abnormal Descemet membrane morphology
HP:0011491	Reduced number of corneal endothelial cells
HP:0011492	Abnormality of corneal stroma
HP:0011493	Central opacification of the cornea
HP:0011494	Generalized opacification of the cornea
HP:0011495	Abnormal corneal epithelium morphology
HP:0011496	Corneal neovascularization
HP:0011497	Iris neovascularization
HP:0011498	obsolete Partial aniridia
HP:0011499	Mydriasis
HP:0011500	Polycoria
HP:0011501	Anterior lenticonus
HP:0011502	Posterior lenticonus
HP:0011503	Aplasia of the fovea
HP:0011504	Bull's eye maculopathy
HP:0011505	Cystoid macular edema
HP:0011506	Choroidal neovascularization
HP:0011507	Macular flecks
HP:0011508	Macular hole
HP:0011509	Macular hyperpigmentation
HP:0011510	Drusen
HP:0011511	Macular schisis
HP:0011512	Hyperpigmentation of the fundus
HP:0011513	Retinal cavernous angioma
HP:0011514	Abnormality of binocular vision
HP:0011515	Abnormal stereopsis
HP:0011516	Achromatopsia
HP:0011517	Cone monochromacy
HP:0011518	Dichromacy
HP:0011519	Anomalous trichromacy
HP:0011520	Deuteranomaly
HP:0011521	Deuteranopia
HP:0011522	Protanopia
HP:0011523	Iris cyst
HP:0011524	Iris melanoma
HP:0011525	Iris nevus
HP:0011526	Abnormality of lens shape
HP:0011527	Lentiglobus
HP:0011528	Solitary congenital hypertrophy of retinal pigment epithelium
HP:0011529	Multiple bilateral congenital hypertrophy of retinal pigment epithelium
HP:0011530	Retinal hole
HP:0011531	Vitritis
HP:0011532	Subretinal exudate
HP:0011533	Snowflake vitreoretinal degeneration
HP:0011534	Abnormal spatial orientation of the cardiac segments
HP:0011535	Abnormal atrial arrangement
HP:0011536	Right atrial isomerism
HP:0011537	Left atrial isomerism
HP:0011538	Atrial situs inversus
HP:0011539	Atrial situs ambiguous
HP:0011540	Congenitally corrected transposition of the great arteries
HP:0011541	Criss-cross atrioventricular valves
HP:0011542	Criss-cross atrioventricular valves with superior-inferior ventricles
HP:0011543	Superior-inferior ventricles without criss-cross atrioventricular valves
HP:0011544	L-looping of the right ventricle
HP:0011545	Abnormal connection of the cardiac segments
HP:0011546	Abnormal atrioventricular connection
HP:0011547	Absent left sided atrioventricular connection
HP:0011548	Absent right sided atrioventricular connection
HP:0011549	Univentricular heart with absent left sided atrioventricular connection
HP:0011550	Biventricular heart with straddling right sided atrioventricular valve and absent left sided atrioventricular connection
HP:0011551	Right sided atrium to left ventricle and absent left sided atrioventricular connection
HP:0011552	Ambiguous atrioventricular connection
HP:0011553	Discordant atrioventricular connection
HP:0011554	Double inlet atrioventricular connection
HP:0011555	Double inlet left ventricle
HP:0011556	Double inlet right ventricle
HP:0011557	Double inlet to single ventricle of indeterminate morphology
HP:0011558	Double inlet to single ventricle with common atrioventricular orifice
HP:0011559	Double inlet to single ventricle with two atrioventricular valves
HP:0011560	Mitral atresia
HP:0011561	Overriding atrioventricular valve
HP:0011562	Straddling atrioventricular valve
HP:0011563	Abnormal ventriculoarterial connection
HP:0011564	Mitral valve arcade
HP:0011565	Common atrium
HP:0011566	Cor triatriatum dexter
HP:0011567	Sinus venosus atrial septal defect
HP:0011568	Double orifice mitral valve
HP:0011569	Cleft anterior mitral valve leaflet
HP:0011570	Congenital mitral stenosis
HP:0011571	Parachute mitral valve
HP:0011572	Supramitral ring
HP:0011573	Hypoplastic tricuspid valve
HP:0011574	Imperforate atrioventricular valve
HP:0011575	Imperforate tricuspid valve
HP:0011576	Intermediate atrioventricular canal defect
HP:0011577	Partial atrioventricular canal defect
HP:0011578	Transitional atrioventricular canal defect
HP:0011579	Unbalanced atrioventricular canal defect
HP:0011580	Short chordae tendineae of the mitral valve
HP:0011581	Double outlet left ventricle
HP:0011582	Abdominal ectopia cordis
HP:0011583	Cervical ectopia cordis
HP:0011584	Thoracocervical ectopia cordis
HP:0011585	Thoracic ectopia cordis
HP:0011586	Thoracoabdominal ectopia cordis
HP:0011587	Abnormal branching pattern of the aortic arch
HP:0011588	Cervical aortic arch
HP:0011589	Common origin of the right brachiocephalic artery and left common carotid artery
HP:0011590	Double aortic arch
HP:0011591	Left aortic arch with cervical origin of the right subclavian artery
HP:0011592	Left aortic arch with isolated subclavian artery
HP:0011593	Left aortic arch with retroesophageal diverticulum of Kommerell
HP:0011594	Right aortic arch with retroesophageal diverticulum of Kommerell
HP:0011595	Left aortic arch with retroesophageal right subclavian artery
HP:0011596	Left aortic arch with right descending aorta and right ductus arteriosus
HP:0011597	Right aortic arch with left descending aorta and left ductus arteriosus
HP:0011598	Right aortic arch with retroesophageal left subclavian artery
HP:0011599	Mesocardia
HP:0011600	Abnormal direction of ventricular apex
HP:0011601	Rightward direction of ventricular apex
HP:0011602	Midline direction of ventricular apex
HP:0011603	Congenital malformation of the great arteries
HP:0011604	Aortopulmonary window
HP:0011605	Congenitally corrected transposition of the great arteries with ventricular septal defect
HP:0011606	obsolete Transposition of the great arteries with intact ventricular septum
HP:0011607	obsolete Transposition of the great arteries with ventricular septal defect
HP:0011608	Type II truncus arteriosus
HP:0011609	Type III truncus arteriosus
HP:0011610	Type IV truncus arteriosus
HP:0011611	Interrupted aortic arch
HP:0011612	Interrupted aortic arch type A
HP:0011613	Interrupted aortic arch type B
HP:0011614	Interrupted aortic arch type C
HP:0011615	Abnormal pulmonary situs morphology
HP:0011616	Pulmonary situs inversus
HP:0011617	Pulmonary situs ambiguus
HP:0011618	Pulmonary situs ambiguus with bilateral morphologic right lungs
HP:0011619	Pulmonary situs ambiguus with bilateral morphologic left lungs
HP:0011620	Abnormality of abdominal situs
HP:0011621	Gerbode ventricular septal defect
HP:0011622	Inlet ventricular septal defect
HP:0011623	Muscular ventricular septal defect
HP:0011624	Apical muscular ventricular septal defect
HP:0011625	Multiple muscular ventricular septal defects
HP:0011626	Scimitar anomaly
HP:0011627	Aorto-ventricular tunnel
HP:0011628	Congenital defect of the pericardium
HP:0011629	Total absence of the pericardium
HP:0011630	Complete diaphragmatic absence of pericardium
HP:0011631	Complete right sided absence of pericardium
HP:0011632	Partial right sided absence of pericardium
HP:0011633	Complete left sided absence of pericardium
HP:0011634	Partial left sided absence of pericardium
HP:0011635	Partial diaphragmatic absence of pericardium
HP:0011636	Abnormal coronary artery origin
HP:0011637	Anomalous origin of coronary artery from the pulmonary artery
HP:0011638	Anomalous origin of left coronary artery from the pulmonary artery
HP:0011639	Anomalous origin of right coronary artery from the pulmonary artery
HP:0011640	Single coronary artery origin
HP:0011641	Coronary artery fistula
HP:0011642	Abnormal coronary sinus morphology
HP:0011643	Coronary sinus atrial septal defect
HP:0011644	Coronary sinus diverticulum
HP:0011645	Dilatation of the sinus of Valsalva
HP:0011646	Juxtaductal coarctation of the aorta
HP:0011647	Postductal coarctation of the aorta
HP:0011648	Patent ductus arteriosus after birth at term
HP:0011649	Patent ductus arteriosus after premature birth
HP:0011650	Bilateral ductus arteriosus
HP:0011651	Double outlet right ventricle with doubly committed ventricular septal defect and pulmonary stenosis
HP:0011652	Double outlet right ventricle with doubly committed ventricular septal defect without pulmonary stenosis
HP:0011653	Double outlet right ventricle with non-committed ventricular septal defect and pulmonary stenosis
HP:0011654	Double outlet right ventricle with non-committed ventricular septal defect without pulmonary stenosis
HP:0011655	Double outlet right ventricle with subaortic ventricular septal defect and pulmonary stenosis
HP:0011656	Double outlet right ventricle with subaortic ventricular septal defect without pulmonary stenosis
HP:0011657	Double outlet right ventricle with subpulmonary ventricular septal defect and pulmonary stenosis
HP:0011658	Double outlet right ventricle with subpulmonary ventricular septal defect without pulmonary stenosis
HP:0011659	Tetralogy of Fallot with absent pulmonary valve
HP:0011660	Anomalous origin of one pulmonary artery from ascending aorta
HP:0011661	Anomalous origin of left pulmonary artery from ascending aorta
HP:0011662	Tricuspid atresia
HP:0011663	Right ventricular cardiomyopathy
HP:0011664	Left ventricular noncompaction cardiomyopathy
HP:0011665	Takotsubo cardiomyopathy
HP:0011666	Absent right superior vena cava
HP:0011667	Bilateral superior vena cava with bridging vein
HP:0011668	Bilateral superior vena cava with no bridging vein
HP:0011669	Left superior vena cava draining directly to the left atrium
HP:0011670	Left superior vena cava draining to coronary sinus
HP:0011671	Interrupted inferior vena cava with azygous continuation
HP:0011672	Cardiac myxoma
HP:0011673	Cardiac hemangioma
HP:0011674	Cardiac teratoma
HP:0011675	Arrhythmia
HP:0011676	Tetralogy of Fallot with absent subarterial conus
HP:0011677	Tetralogy of Fallot with atrioventricular canal defect
HP:0011678	Tetralogy of Fallot with pulmonary atresia and major aortopulmonary collateral arteries
HP:0011679	Tetralogy of Fallot with pulmonary stenosis
HP:0011680	Single ventricle of indeterminate morphology
HP:0011681	Subarterial ventricular septal defect
HP:0011682	Perimembranous ventricular septal defect
HP:0011683	Restrictive ventricular septal defect
HP:0011684	Non-restrictive ventricular septal defect
HP:0011685	Infra-aortic superior vena cava
HP:0011686	Abnormal coronary artery course
HP:0011687	AV nodal tachycardia
HP:0011688	Supraventricular tachycardia with an accessory connection mediated pathway
HP:0011689	Supraventricular tachycardia with a concealed accessory connection
HP:0011690	Permanent junctional reciprocating tachycardia
HP:0011691	Supraventricular tachycardia with a concealed accessory pathway on the left free wall
HP:0011692	Supraventricular tachycardia with a concealed accessory pathway on the right free wall
HP:0011693	Supraventricular tachycardia with a concealed accessory pathway on the septum
HP:0011694	Supraventricular tachycardia with a manifest accessory pathway
HP:0011695	Cerebellar hemorrhage
HP:0011696	Supraventricular tachycardia with a manifest accessory pathway on the left free wall
HP:0011697	Supraventricular tachycardia with a manifest accessory pathway on the right free wall
HP:0011698	Supraventricular tachycardia with a manifest accessory pathway on the septum
HP:0011699	Atrial reentry tachycardia
HP:0011700	Automatic atrial tachycardia
HP:0011701	Multifocal atrial tachycardia
HP:0011702	Abnormal electrophysiology of sinoatrial node origin
HP:0011703	Sinus tachycardia
HP:0011704	Sick sinus syndrome
HP:0011705	First degree atrioventricular block
HP:0011706	Second degree atrioventricular block
HP:0011707	Mobitz I atrioventricular block
HP:0011708	Mobitz II atrioventricular block
HP:0011709	Atrioventricular dissociation
HP:0011710	Bundle branch block
HP:0011711	Left anterior fascicular block
HP:0011712	Right bundle branch block
HP:0011713	Left bundle branch block
HP:0011714	Libman-Sacks lesions
HP:0011715	Trifascicular block
HP:0011716	Junctional ectopic tachycardia
HP:0011717	Atrioventricular reentrant tachycardia
HP:0011718	Abnormality of the pulmonary veins
HP:0011719	Supracardiac total anomalous pulmonary venous connection
HP:0011720	Cardiac total anomalous pulmonary venous connection
HP:0011721	Infracardiac total anomalous pulmonary venous connection
HP:0011722	Mixed total anomalous pulmonary venous connection
HP:0011723	Congenital malformation of the right heart
HP:0011724	Uhl's anomaly
HP:0011725	Chaotic multifocal atrial tachycardia
HP:0011726	Persistent fetal circulation
HP:0011727	Peroneal muscle weakness
HP:0011728	Elbow clonus
HP:0011729	Abnormality of joint mobility
HP:0011730	Abnormality of central sensory function
HP:0011731	Abnormality of circulating cortisol level
HP:0011732	Abnormality of adrenal morphology
HP:0011733	Abnormality of adrenal physiology
HP:0011734	Central adrenal insufficiency
HP:0011735	Adrenocorticotropin deficient adrenal insufficiency
HP:0011736	Primary hyperaldosteronism
HP:0011737	Corticotropin-releasing hormone deficient adrenal insufficiency
HP:0011738	Corticotropin-releasing hormone receptor defect
HP:0011739	Dexamethasone-suppresible primary hyperaldosteronism
HP:0011740	Glucocortocoid-insensitive primary hyperaldosteronism
HP:0011741	Secondary hyperaldosteronism
HP:0011742	Ectopic adrenal gland
HP:0011743	Adrenal gland agenesis
HP:0011744	Secondary hypercortisolism
HP:0011745	Non-secretory adrenocortical adenoma
HP:0011746	Secretory adrenocortical adenoma
HP:0011747	Abnormality of the anterior pituitary
HP:0011748	Adrenocorticotropic hormone deficiency
HP:0011749	Adrenocorticotropic hormone excess
HP:0011750	Neoplasm of the anterior pituitary
HP:0011751	Abnormality of the posterior pituitary
HP:0011752	Neoplasm of the posterior pituitary
HP:0011753	Posterior pituitary dysgenesis
HP:0011754	Pituicytoma
HP:0011755	Ectopic posterior pituitary
HP:0011756	Posterior pituitary agenesis
HP:0011757	Posterior pituitary hypoplasia
HP:0011758	Pituitary acidophilic stem cell adenoma
HP:0011759	Pituitary gonadotropic cell adenoma
HP:0011760	Pituitary growth hormone cell adenoma
HP:0011761	Pituitary null cell adenoma
HP:0011762	Pituitary thyrotropic cell adenoma
HP:0011763	Pituitary carcinoma
HP:0011764	Pituitary spindle cell oncocytoma
HP:0011765	obsolete Ectopic anterior pituitary
HP:0011766	Abnormality of the parathyroid morphology
HP:0011767	Abnormality of the parathyroid physiology
HP:0011768	Parathyroid dysgenesis
HP:0011769	Ectopic parathyroid
HP:0011770	Tertiary hyperparathyroidism
HP:0011771	Autoimmune hypoparathyroidism
HP:0011772	Abnormality of thyroid morphology
HP:0011773	Uninodular goiter
HP:0011774	Thyroid follicular adenoma
HP:0011775	Thyroid macrofollicular adenoma
HP:0011776	Thyroid microfollicular adenoma
HP:0011777	Thyroid papillary adenoma
HP:0011778	Thyroid atypical adenoma
HP:0011779	Anaplastic thyroid carcinoma
HP:0011780	Thyroid hemiagenesis
HP:0011781	Thyroid C cell hyperplasia
HP:0011782	Thyroid crisis
HP:0011783	Thyrotoxicosis from ectopic thyroid tissue
HP:0011784	Thyrotoxicosis with diffuse goiter
HP:0011785	Thyrotoxicosis with toxic multinodular goitre
HP:0011786	Thyrotoxicosis with toxic single thyroid nodule
HP:0011787	Central hypothyroidism
HP:0011788	Increased serum free triiodothyronine
HP:0011789	Thyroid-stimulating hormone receptor defect
HP:0011790	Activating thyroid-stimulating hormone receptor defect
HP:0011791	Inactivating thyroid-stimulating hormone receptor defect
HP:0011792	Neoplasm by histology
HP:0011793	Neoplasm by anatomical site
HP:0011794	Embryonal renal neoplasm
HP:0011795	Intralobar nephroblastomatosis
HP:0011796	Perilobar nephroblastomatosis
HP:0011797	Papillary renal cell carcinoma type 1
HP:0011798	Renal oncocytoma
HP:0011799	Abnormality of facial soft tissue
HP:0011800	Midface retrusion
HP:0011801	Enlargement of parotid gland
HP:0011802	Hamartoma of tongue
HP:0011803	Bifid nose
HP:0011804	Abnormality of muscle physiology
HP:0011805	Abnormal muscle morphology
HP:0011807	Type 1 muscle fiber atrophy
HP:0011808	Decreased patellar reflex
HP:0011809	Paradoxical myotonia
HP:0011810	Impaired two-point discrimination
HP:0011811	Impaired touch localization
HP:0011812	Agraphesthesia
HP:0011813	Increased cerebral lipofuscin
HP:0011814	Increased urinary hypoxanthine
HP:0011815	Cephalocele
HP:0011816	Parietal encephalocele
HP:0011817	Basal encephalocele
HP:0011818	Nasofrontal encephalocele
HP:0011819	Submucous cleft soft palate
HP:0011820	Membranous choanal atresia
HP:0011821	Abnormality of facial skeleton
HP:0011822	Broad chin
HP:0011823	Chin with horizontal crease
HP:0011824	Chin with H-shaped crease
HP:0011825	Tented philtrum
HP:0011826	Philtrum with midline raphe
HP:0011827	Malaligned philtral ridges
HP:0011828	Midline sinus of philtrum
HP:0011829	Narrow philtrum
HP:0011830	Abnormal oral mucosa morphology
HP:0011831	Deviated nasal tip
HP:0011832	Narrow nasal tip
HP:0011833	Overhanging nasal tip
HP:0011834	Moyamoya phenomenon
HP:0011835	Absent scaphoid
HP:0011836	Delayed talus ossification
HP:0011837	Partial IgA deficiency
HP:0011838	Sclerodactyly
HP:0011839	Abnormal T cell count
HP:0011840	Abnormality of T cell physiology
HP:0011841	Ventricular flutter
HP:0011842	Abnormality of skeletal morphology
HP:0011843	Abnormality of skeletal physiology
HP:0011844	Abnormal appendicular skeleton morphology
HP:0011845	Short second metatarsal
HP:0011846	Osteoblastoma
HP:0011847	Giant cell tumor of bone
HP:0011848	Abdominal colic
HP:0011849	Abnormal bone ossification
HP:0011850	Parotitis
HP:0011851	Hemopericardium
HP:0011852	Chylopericardium
HP:0011853	Serous pericardial effusion
HP:0011854	Hemoperitoneum
HP:0011855	Pharyngeal edema
HP:0011856	Pica
HP:0011857	Plasmacytoma
HP:0011858	Reduced factor IX activity
HP:0011859	Punctate keratitis
HP:0011860	Metaphyseal dappling
HP:0011861	Bilateral trilobed lungs
HP:0011862	Abnormal bone collagen fibril morphology
HP:0011863	Abnormal sternal ossification
HP:0011864	Elevated plasma pyrophosphate
HP:0011867	Abnormality of the wing of the ilium
HP:0011868	Sciatica
HP:0011869	Abnormal platelet function
HP:0011870	Impaired arachidonic acid-induced platelet aggregation
HP:0011871	Impaired ristocetin-induced platelet aggregation
HP:0011872	Impaired thrombin-induced platelet aggregation
HP:0011873	Abnormal platelet count
HP:0011874	Heparin-induced thrombocytopenia
HP:0011875	Abnormal platelet morphology
HP:0011876	Abnormal platelet volume
HP:0011877	Increased mean platelet volume
HP:0011878	Abnormal platelet membrane protein expression
HP:0011879	Decreased platelet glycoprotein Ib-IX-V
HP:0011880	Acute disseminated intravascular coagulation
HP:0011881	Decreased platelet glycoprotein VI
HP:0011882	Decreased platelet P2Y12 receptor
HP:0011883	Abnormal platelet granules
HP:0011884	Abnormal umbilical stump bleeding
HP:0011885	Hemorrhage of the eye
HP:0011886	Hyphema
HP:0011887	Choroid hemorrhage
HP:0011888	Bleeding requiring red cell transfusion
HP:0011889	Bleeding with minor or no trauma
HP:0011890	Prolonged bleeding following procedure
HP:0011891	Post-partum hemorrhage
HP:0011892	Vitamin K deficiency
HP:0011893	Abnormal leukocyte count
HP:0011894	Impaired thromboxane A2 agonist-induced platelet aggregation
HP:0011895	Anemia due to reduced life span of red cells
HP:0011896	Subconjunctival hemorrhage
HP:0011897	Neutrophilia
HP:0011898	Abnormality of circulating fibrinogen
HP:0011899	Hyperfibrinogenemia
HP:0011900	Hypofibrinogenemia
HP:0011901	Dysfibrinogenemia
HP:0011902	Abnormal hemoglobin
HP:0011903	HbH hemoglobin
HP:0011904	Persistence of hemoglobin F
HP:0011905	Reduced hemoglobin A
HP:0011906	Reduced beta/alpha synthesis ratio
HP:0011907	Reduced alpha/beta synthesis ratio
HP:0011908	Unilateral radial aplasia
HP:0011909	Flattened metacarpal heads
HP:0011910	Shortening of all phalanges of fingers
HP:0011911	Abnormality of metacarpophalangeal joint
HP:0011912	Abnormality of the glenoid fossa
HP:0011913	Lumbar hypertrichosis
HP:0011914	Thoracic hypertrichosis
HP:0011915	Cardiovascular calcification
HP:0011916	Toe extensor amyotrophy
HP:0011917	Short 5th toe
HP:0011918	Clinodactyly of the 4th toe
HP:0011919	Pleural empyema
HP:0011920	Transudative pleural effusion
HP:0011921	Exudative pleural effusion
HP:0011922	Abnormal activity of mitochondrial respiratory chain
HP:0011923	Decreased activity of mitochondrial complex I
HP:0011924	Decreased activity of mitochondrial complex III
HP:0011925	Decreased activity of mitochondrial ATP synthase complex
HP:0011926	Proximal placement of hallux
HP:0011927	Short digit
HP:0011928	Short proximal phalanx of toe
HP:0011929	Hypersegmentation of proximal phalanx of third finger
HP:0011930	Hyperextensible skin of chest
HP:0011931	Abnormality of the cerebellar peduncle
HP:0011932	Abnormality of the superior cerebellar peduncle
HP:0011933	Elongated superior cerebellar peduncle
HP:0011934	Dilatation of mesenteric artery
HP:0011935	Decreased urinary urate
HP:0011936	Decreased plasma total carnitine
HP:0011937	Hypoplastic fifth toenail
HP:0011939	3-4 finger cutaneous syndactyly
HP:0011940	Anterior wedging of T12
HP:0011941	Anterior wedging of L2
HP:0011942	Increased urinary sulfite
HP:0011943	Increased urinary thiosulfate
HP:0011944	Small vessel vasculitis
HP:0011945	Bronchiolitis obliterans organizing pneumonia
HP:0011946	Bronchiolitis obliterans
HP:0011947	Respiratory tract infection
HP:0011948	Acute respiratory tract infection
HP:0011949	Acute infectious pneumonia
HP:0011950	Bronchiolitis
HP:0011951	Aspiration pneumonia
HP:0011952	Acute aspiration pneumonia
HP:0011953	Pulmonary lymphoma
HP:0011954	Nodular regenerative hyperplasia of liver
HP:0011955	Hepatic granulomatosis
HP:0011956	Intestinal lymphoid nodular hyperplasia
HP:0011957	Abnormality of the pectoral muscle
HP:0011958	Retinal perforation
HP:0011959	Unilateral hypoplasia of pectoralis major muscle
HP:0011960	Substantia nigra gliosis
HP:0011961	Non-obstructive azoospermia
HP:0011962	Obstructive azoospermia
HP:0011963	Pretesticular azoospermia
HP:0011964	Intermittent painful muscle spasms
HP:0011965	Abnormality of citrulline metabolism
HP:0011966	Elevated plasma citrulline
HP:0011967	Hypocupremia
HP:0011968	Feeding difficulties
HP:0011969	Elevated circulating luteinizing hormone level
HP:0011970	Cerebral amyloid angiopathy
HP:0011971	Dermatographic urticaria
HP:0011972	Hypoglycorrhachia
HP:0011973	Paroxysmal lethargy
HP:0011974	Myelofibrosis
HP:0011975	Aminoglycoside-induced hearing loss
HP:0011976	Elevated urinary catecholamines
HP:0011977	Elevated urinary homovanillic acid
HP:0011978	Elevated urinary vanillylmandelic acid
HP:0011979	Elevated urinary dopamine
HP:0011980	Cholesterol gallstones
HP:0011981	Pigment gallstones
HP:0011982	Black pigment gallstones
HP:0011983	Brown pigment gallstones
HP:0011984	Atretic gallbladder
HP:0011985	Acholic stools
HP:0011986	Ectopic ossification
HP:0011987	Ectopic ossification in muscle tissue
HP:0011988	Ectopic ossification in tendon tissue
HP:0011989	Ectopic ossification in ligament tissue
HP:0011990	Abnormality of neutrophil physiology
HP:0011991	Abnormal neutrophil count
HP:0011992	Abnormality of neutrophil morphology
HP:0011993	Impaired neutrophil bactericidal activity
HP:0011994	Abnormal atrial septum morphology
HP:0011995	Atrial septal dilatation
HP:0011996	Elevated coagulation factor V activity
HP:0011997	Postprandial hyperlactemia
HP:0011998	Postprandial hyperglycemia
HP:0011999	Paranoia
HP:0012000	EEG with generalized spikes
HP:0012001	EEG with generalized polyspikes
HP:0012002	Experiential auras
HP:0012003	Affective auras
HP:0012004	Mnemonic auras
HP:0012005	Deja vu
HP:0012006	Jamais vu
HP:0012007	Hallucinatory auras
HP:0012008	Illusory auras
HP:0012009	EEG with central focal spike waves
HP:0012010	EEG with frontal focal spike waves
HP:0012011	EEG with occipital focal spike waves
HP:0012012	EEG with parietal focal spike waves
HP:0012013	EEG with temporal focal spike waves
HP:0012014	EEG with central focal spikes
HP:0012015	EEG with frontal focal spikes
HP:0012016	EEG with occipital focal spikes
HP:0012017	EEG with parietal focal spikes
HP:0012018	EEG with temporal focal spikes
HP:0012019	Lens luxation
HP:0012020	Right aortic arch
HP:0012021	Persistent patent ductus venosus
HP:0012022	Congenital portosystemic venous shunt
HP:0012023	Galactosuria
HP:0012024	Hypergalactosemia
HP:0012025	Abnormality of ornithine metabolism
HP:0012026	Hyperornithinemia
HP:0012027	Laryngeal edema
HP:0012028	Hepatocellular adenoma
HP:0012029	Abnormality of urine hormone level
HP:0012030	Increased urinary cortisol level
HP:0012031	Lipomatous tumor
HP:0012032	Lipoma
HP:0012033	Sacral lipoma
HP:0012034	Liposarcoma
HP:0012035	Steatocystoma multiplex
HP:0012036	Sternocleidomastoid amyotrophy
HP:0012037	Pectoralis amyotrophy
HP:0012038	Corneal guttata
HP:0012039	Descemet Membrane Folds
HP:0012040	Corneal stromal edema
HP:0012041	Decreased fertility in males
HP:0012042	Aspirin-induced asthma
HP:0012043	Pendular nystagmus
HP:0012044	Seesaw nystagmus
HP:0012045	Retinal flecks
HP:0012046	Areflexia of upper limbs
HP:0012047	Hemeralopia
HP:0012048	Oromandibular dystonia
HP:0012049	Laryngeal dystonia
HP:0012050	Anasarca
HP:0012051	Reactive hypoglycemia
HP:0012052	Low serum calcitriol
HP:0012053	Low serum calcifediol
HP:0012054	Choroidal melanoma
HP:0012055	Ciliary body melanoma
HP:0012056	Cutaneous melanoma
HP:0012057	Superficial spreading melanoma
HP:0012058	Nodular melanoma
HP:0012059	Lentigo maligna melanoma
HP:0012060	Acral lentiginous melanoma
HP:0012061	Urinary excretion of sialylated oligosaccharides
HP:0012062	Bone cyst
HP:0012063	Aneurysmal bone cyst
HP:0012064	Unicameral bone cyst
HP:0012065	Multiple bony cystic lesions
HP:0012066	Increased urinary disaccharide excretion
HP:0012067	Glycopeptiduria
HP:0012068	Aspartylglucosaminuria
HP:0012069	Keratan sulfate excretion in urine
HP:0012070	Chondroitin sulfate excretion in urine
HP:0012071	Abnormality of acetylcarnitine metabolism
HP:0012072	Aciduria
HP:0012073	Abnormal urinary acylglycine profile
HP:0012074	Tonic pupil
HP:0012075	Personality disorder
HP:0012076	Borderline personality disorder
HP:0012077	Histrionic personality disorder
HP:0012078	Motor conduction block
HP:0012079	Abnormality of central motor conduction
HP:0012080	Cerebellar granular layer atrophy
HP:0012081	Enlarged cerebellum
HP:0012082	Cerebellar Purkinje layer atrophy
HP:0012083	Ubiquitin-positive cerebral inclusion bodies
HP:0012084	Abnormality of skeletal muscle fiber size
HP:0012085	Pyuria
HP:0012086	Abnormal urinary color
HP:0012087	Abnormal mitochondrial shape
HP:0012088	Abnormal urinary odor
HP:0012089	Arteritis
HP:0012090	Abnormal pancreas morphology
HP:0012091	Abnormality of pancreas physiology
HP:0012092	Abnormality of exocrine pancreas physiology
HP:0012093	Abnormality of endocrine pancreas physiology
HP:0012094	Abnormal pancreas size
HP:0012095	Multiple joint dislocation
HP:0012096	Intracranial epidermoid cyst
HP:0012097	Intracranial dermoid cyst
HP:0012098	Edema of the dorsum of feet
HP:0012099	Abnormality of circulating catecholamine level
HP:0012100	Abnormal circulating creatinine level
HP:0012101	Decreased serum creatinine
HP:0012102	Abnormal mitochondrial number
HP:0012103	Abnormality of the mitochondrion
HP:0012104	Parietal cortical atrophy
HP:0012105	Occipital cortical atrophy
HP:0012106	Rhizomelic leg shortening
HP:0012107	Increased fibular diameter
HP:0012108	Open angle glaucoma
HP:0012109	Angle closure glaucoma
HP:0012110	Hypoplasia of the pons
HP:0012111	Abnormality of circulating glucocorticoid level
HP:0012112	Abnormality of circulating corticosterone level
HP:0012113	Abnormality of creatine metabolism
HP:0012114	Endometrial carcinoma
HP:0012115	Hepatitis
HP:0012116	Abnormal albumin level
HP:0012117	Hyperalbuminemia
HP:0012118	Laryngeal carcinoma
HP:0012119	Methemoglobinemia
HP:0012120	Methylmalonic aciduria
HP:0012121	Panuveitis
HP:0012122	Anterior uveitis
HP:0012123	Posterior uveitis
HP:0012124	Intermediate uveitis
HP:0012125	Prostate cancer
HP:0012126	Stomach cancer
HP:0012127	Uraciluria
HP:0012128	Basal ganglia necrosis
HP:0012129	Abnormality of bone marrow stromal cells
HP:0012130	Abnormal erythroid lineage cell morphology
HP:0012131	Abnormal number of erythroid precursors
HP:0012132	Erythroid hyperplasia
HP:0012133	Erythroid hypoplasia
HP:0012134	Dysplastic erythropoesis
HP:0012135	Abnormal granulocytopoietic cell morphology
HP:0012136	Dysplastic granulopoesis
HP:0012137	Abnormal number of granulocyte precursors
HP:0012138	Granulocytic hyperplasia
HP:0012139	Granulocytic hypoplasia
HP:0012140	obsolete Abnormality of cells of the lymphoid lineage
HP:0012142	Pancreatic squamous cell carcinoma
HP:0012143	Abnormal megakaryocyte morphology
HP:0012144	Abnormality monocyte morphology
HP:0012145	Abnormality of multiple cell lineages in the bone marrow
HP:0012146	Abnormality of von Willebrand factor
HP:0012147	Reduced quantity of Von Willebrand factor
HP:0012148	Multiple lineage myelodysplasia
HP:0012149	Bilineage myelodysplasia
HP:0012150	Single lineage myelodysplasia
HP:0012151	Hemothorax
HP:0012152	Foveoschisis
HP:0012153	Hypotriglyceridemia
HP:0012154	Anhedonia
HP:0012155	Decreased corneal sensation
HP:0012156	Hemophagocytosis
HP:0012157	Subcortical cerebral atrophy
HP:0012158	Carotid artery dissection
HP:0012159	Internal carotid artery dissection
HP:0012160	Intracranial internal carotid artery dissection
HP:0012161	External carotid artery dissection
HP:0012162	Common carotid artery dissection
HP:0012163	Carotid artery dilatation
HP:0012164	Asterixis
HP:0012165	Oligodactyly
HP:0012166	Skin-picking
HP:0012167	Hair-pulling
HP:0012168	Head-banging
HP:0012169	Self-biting
HP:0012170	Nail-biting
HP:0012171	Stereotypical hand wringing
HP:0012172	Stereotypical body rocking
HP:0012173	Orthostatic tachycardia
HP:0012174	Glioblastoma multiforme
HP:0012175	Resistance to activated protein C
HP:0012176	Abnormal natural killer cell morphology
HP:0012177	Abnormal natural killer cell physiology
HP:0012178	Reduced natural killer cell activity
HP:0012179	Craniofacial dystonia
HP:0012180	Cystic medial necrosis
HP:0012181	Entrapment neuropathy
HP:0012182	Oropharyngeal squamous cell carcinoma
HP:0012183	Hyperplastic colonic polyposis
HP:0012184	Increased HDL cholesterol concentration
HP:0012185	Constrictive median neuropathy
HP:0012186	Entrapment neuropathy of the ulnar nerve at elbow
HP:0012187	Increased erythrocyte protoporphyrin concentration
HP:0012188	Hyperemesis gravidarum
HP:0012189	Hodgkin lymphoma
HP:0012190	T-cell lymphoma
HP:0012191	B-cell lymphoma
HP:0012192	Cutaneous T-cell lymphoma
HP:0012193	Anaplastic large-cell lymphoma
HP:0012194	Episodic hemiplegia
HP:0012195	Irregular respiration
HP:0012196	Cheyne-Stokes respiration
HP:0012197	Insulinoma
HP:0012198	Juvenile colonic polyposis
HP:0012199	Cluster headache
HP:0012200	Abnormality of prothrombin
HP:0012201	Reduced prothrombin activity
HP:0012202	Increased serum bile acid concentration
HP:0012203	Onychomycosis
HP:0012204	Recurrent vulvovaginal candidiasis
HP:0012205	Globozoospermia
HP:0012206	Abnormal sperm motility
HP:0012207	Reduced sperm motility
HP:0012208	Nonmotile sperm
HP:0012209	Juvenile myelomonocytic leukemia
HP:0012210	Abnormal renal morphology
HP:0012211	Abnormal renal physiology
HP:0012212	Abnormal glomerular filtration rate
HP:0012213	Decreased glomerular filtration rate
HP:0012214	Increased glomerular filtration rate
HP:0012215	Testicular microlithiasis
HP:0012216	Entrapment neuropathy of suprascapular nerve
HP:0012217	Increased urinary porphobilinogen
HP:0012218	Alveolar soft part sarcoma
HP:0012219	Erythema nodosum
HP:0012220	Non-caseating epithelioid cell granulomatosis
HP:0012221	Pretibial blistering
HP:0012222	Arachnoid hemangiomatosis
HP:0012223	Splenic rupture
HP:0012224	Circulating immune complexes
HP:0012225	Oligodontia of primary teeth
HP:0012226	Ovarian teratoma
HP:0012227	Urethral stricture
HP:0012228	Tension-type headache
HP:0012229	CSF pleocytosis
HP:0012230	Rhegmatogenous retinal detachment
HP:0012231	Exudative retinal detachment
HP:0012232	Shortened QT interval
HP:0012233	Intramuscular hematoma
HP:0012234	Agranulocytosis
HP:0012235	Drug-induced agranulocytosis
HP:0012236	Elevated sweat chloride
HP:0012237	Urocanic aciduria
HP:0012238	Increased circulating chylomicron concentration
HP:0012239	Atransferrinemia
HP:0012240	Increased intramyocellular lipid droplets
HP:0012241	Levator palpebrae superioris atrophy
HP:0012242	Superior rectus atrophy
HP:0012243	Abnormal reproductive system morphology
HP:0012244	Abnormal sex determination
HP:0012245	Sex reversal
HP:0012246	Oculomotor nerve palsy
HP:0012247	Specific anosmia
HP:0012248	Prolonged PR interval
HP:0012249	Abnormal ST segment
HP:0012250	ST segment depression
HP:0012251	ST segment elevation
HP:0012252	Abnormal respiratory system morphology
HP:0012253	Abnormal respiratory epithelium morphology
HP:0012254	Ewing sarcoma
HP:0012255	Dynein arm defect of respiratory motile cilia
HP:0012256	Absent outer dynein arms
HP:0012257	Absent inner dynein arms
HP:0012258	Abnormal axonemal organization of respiratory motile cilia
HP:0012259	Absent inner and outer dynein arms
HP:0012260	Abnormal central microtubular pair morphology of respiratory motile cilia
HP:0012261	Abnormal respiratory motile cilium physiology
HP:0012262	Abnormal ciliary motility
HP:0012263	Immotile cilia
HP:0012264	Absent central microtubular pair morphology of respiratory motile cilia
HP:0012265	Ciliary dyskinesia
HP:0012266	T-wave alternans
HP:0012267	Absent respiratory ciliary axoneme radial spokes
HP:0012268	Myxoid liposarcoma
HP:0012269	Abnormal muscle glycogen content
HP:0012270	Decreased muscle glycogen content
HP:0012271	Episodic upper airway obstruction
HP:0012272	J wave
HP:0012273	Increased carotid artery intimal medial thickness
HP:0012274	Autosomal dominant inheritance with paternal imprinting
HP:0012275	Autosomal dominant inheritance with maternal imprinting
HP:0012276	Digital flexor tenosynovitis
HP:0012277	Hypoglycinemia
HP:0012278	Abnormality of serine metabolism
HP:0012279	Hyposerinemia
HP:0012280	Hepatic amyloidosis
HP:0012281	Chylous ascites
HP:0012282	Morbilliform rash
HP:0012283	Small distal femoral epiphysis
HP:0012284	Small proximal tibial epiphyses
HP:0012285	Abnormal hypothalamus physiology
HP:0012286	Abnormal hypothalamus morphology
HP:0012287	Hypothalamic luteinizing hormone-releasing hormone deficiency
HP:0012288	Neoplasm of head and neck
HP:0012289	Facial neoplasm
HP:0012290	Mouth neoplasm
HP:0012291	obsolete Tracheal neoplasm
HP:0012292	Fusion of gums
HP:0012293	Abnormal genital pigmentation
HP:0012294	Abnormality of the occipital bone
HP:0012295	Slender middle phalanx of finger
HP:0012296	Slender distal phalanx of finger
HP:0012297	Slender proximal phalanx of finger
HP:0012298	Long middle phalanx of finger
HP:0012299	Long distal phalanx of finger
HP:0012300	Ureteral agenesis
HP:0012301	Type II transferrin isoform profile
HP:0012302	Herpes simplex encephalitis
HP:0012303	Abnormal aortic arch morphology
HP:0012304	Hypoplastic aortic arch
HP:0012305	Coarctation of the descending aortic arch
HP:0012306	Abnormal rib ossification
HP:0012307	Spatulate ribs
HP:0012308	Decreased serum complement C9
HP:0012309	Cutaneous amyloidosis
HP:0012310	Abnormal monocyte count
HP:0012311	Monocytosis
HP:0012312	Monocytopenia
HP:0012313	Heberden's node
HP:0012314	Bouchard's node
HP:0012315	Histiocytoma
HP:0012316	Fibrous tissue neoplasm
HP:0012317	Sacroiliac arthritis
HP:0012318	Occipital neuralgia
HP:0012319	Absent pigmentation of the abdomen
HP:0012320	Absent pigmentation of the limbs
HP:0012321	D-2-hydroxyglutaric aciduria
HP:0012322	Perifolliculitis
HP:0012323	Sleep myoclonus
HP:0012324	Myeloid leukemia
HP:0012325	Chronic myelomonocytic leukemia
HP:0012326	Abnormal celiac artery morphology
HP:0012327	Celiac artery compression
HP:0012328	Cementoma
HP:0012329	Tufted angioma
HP:0012330	Pyelonephritis
HP:0012331	Abnormal autonomic nervous system morphology
HP:0012332	Abnormal autonomic nervous system physiology
HP:0012333	Abnormal sudomotor regulation
HP:0012334	Extrahepatic cholestasis
HP:0012335	Abnormality of folate metabolism
HP:0012336	Reduced cerebrospinal fluid 5-methyltetrahydrofolate concentration
HP:0012337	Abnormal homeostasis
HP:0012338	Abnormal energy expenditure
HP:0012339	Increased resting energy expenditure
HP:0012340	Decreased resting energy expenditure
HP:0012341	Microprolactinoma
HP:0012342	Macroprolactinoma
HP:0012343	Decreased serum ferritin
HP:0012344	Morphea
HP:0012345	Abnormal glycosylation
HP:0012346	Abnormal protein glycosylation
HP:0012347	Abnormal protein N-linked glycosylation
HP:0012348	Decreased galactosylation of N-linked protein glycosylation
HP:0012349	Abnormal sialylation of N-linked protein glycosylation
HP:0012350	Decreased sialylation of N-linked protein glycosylation
HP:0012351	Increased sialylation of N-linked protein glycosylation
HP:0012352	Abnormal fucosylation of protein N-linked glycosylation
HP:0012353	Decreased fucosylation of N-linked protein glycosylation
HP:0012354	Increased fucosylation of N-linked protein glycosylation
HP:0012355	Abnormal mannosylation of N-linked protein glycosylation
HP:0012356	Decreased mannosylation of N-linked protein glycosylation
HP:0012357	Increased mannosylation of N-linked protein glycosylation
HP:0012358	Abnormal protein O-linked glycosylation
HP:0012359	Abnormal fucosylation of O-linked protein glycosylation
HP:0012360	Decreased fucosylation of O-linked protein glycosylation
HP:0012361	Increased fucosylation of O-linked protein glycosylation
HP:0012362	Abnormal sialylation of O-linked protein glycosylation
HP:0012363	Decreased sialylation of O-linked protein glycosylation
HP:0012364	Decreased urinary potassium
HP:0012365	Hypophosphaturia
HP:0012366	Basilar invagination
HP:0012367	Extra fontanelles
HP:0012368	Flat face
HP:0012369	Abnormality of malar bones
HP:0012370	Prominence of the zygomatic bone
HP:0012371	Hyperplasia of midface
HP:0012372	Abnormal eye morphology
HP:0012373	Abnormal eye physiology
HP:0012374	obsolete Abnormal globe morphology
HP:0012375	Chemosis
HP:0012376	Microphakia
HP:0012377	Hemianopia
HP:0012378	Fatigue
HP:0012379	Abnormal enzyme/coenzyme activity
HP:0012380	Reduced carnitine O-palmitoyltransferase activity
HP:0012381	Delayed self-feeding during toddler years
HP:0012382	Left-to-right shunt
HP:0012383	Bidirectional shunt
HP:0012384	Rhinitis
HP:0012385	Camptodactyly
HP:0012386	Absent hallux
HP:0012387	Bronchitis
HP:0012388	Acute bronchitis
HP:0012389	Appendicular hypotonia
HP:0012390	Anal fissure
HP:0012391	Hyporeflexia of upper limbs
HP:0012392	Jaw hyporeflexia
HP:0012393	Allergy
HP:0012394	Iodine contrast allergy
HP:0012395	Seasonal allergy
HP:0012396	Biliary dyskinesia
HP:0012397	Aortic atherosclerotic lesion
HP:0012398	Peripheral edema
HP:0012399	Pressure ulcer
HP:0012400	Abnormal aldolase level
HP:0012401	Abnormal urine alpha-ketoglutarate concentration
HP:0012402	Increased urine alpha-ketoglutarate concentration
HP:0012403	Decreased urine alpha-ketoglutarate concentration
HP:0012404	Abnormal urine citrate concentration
HP:0012405	Hypocitraturia
HP:0012406	Hypercitraturia
HP:0012407	Scissor gait
HP:0012408	Medullary nephrocalcinosis
HP:0012409	Cortical nephrocalcinosis
HP:0012410	Pure red cell aplasia
HP:0012411	Premature pubarche
HP:0012412	Premature adrenarche
HP:0012413	Notched primary central incisor
HP:0012414	Duodenal atrophy
HP:0012415	Abnormal blood gas level
HP:0012416	Hypercapnia
HP:0012417	Hypocapnia
HP:0012418	Hypoxemia
HP:0012419	Hyperoxemia
HP:0012420	Meconium stained amniotic fluid
HP:0012421	Congenital absence of foreskin
HP:0012422	Villous hypertrophy of choroid plexus
HP:0012423	Colonic inertia
HP:0012424	Chorioretinitis
HP:0012425	Stercoral ulcer
HP:0012426	Optic disc drusen
HP:0012427	Excessive femoral anteversion
HP:0012428	Prominent calcaneus
HP:0012429	Aplasia/Hypoplasia of the cerebral white matter
HP:0012430	Cerebral white matter hypoplasia
HP:0012431	Episodic fatigue
HP:0012432	Chronic fatigue
HP:0012433	Abnormal social behavior
HP:0012434	Delayed social development
HP:0012435	Ventral shortening of foreskin
HP:0012436	Nonocclusive coronary artery atherosclerosis
HP:0012437	Abnormal gallbladder morphology
HP:0012438	Abnormal gallbladder physiology
HP:0012439	Abnormal biliary tract physiology
HP:0012440	Abnormal biliary tract morphology
HP:0012441	Sphincter of Oddi dyskinesia
HP:0012442	Gallbladder dyskinesia
HP:0012443	Abnormality of brain morphology
HP:0012444	Brain atrophy
HP:0012446	Low CSF 5-methyltetrahydrofolate
HP:0012447	Abnormal myelination
HP:0012448	Delayed myelination
HP:0012449	Sacroiliac joint synovitis
HP:0012450	Chronic constipation
HP:0012451	Acute constipation
HP:0012452	Restless legs
HP:0012453	Bilateral wrist flexion contracture
HP:0012454	Unilateral wrist flexion contracture
HP:0012455	obsolete Large artery calcification
HP:0012456	Medial arterial calcification
HP:0012457	Medial calcification of medium-sized arteries
HP:0012458	Medial calcification of small arteries
HP:0012459	Hypnic headache
HP:0012460	Dysmorphic inferior cerebellar vermis
HP:0012461	Bacteriuria
HP:0012462	Chin myoclonus
HP:0012463	Elevated transferrin saturation
HP:0012464	Decreased transferrin saturation
HP:0012465	Elevated hepatic iron concentration
HP:0012466	Chronic respiratory acidosis
HP:0012467	Acute respiratory acidosis
HP:0012468	Chronic acidosis
HP:0012469	Infantile spasms
HP:0012470	Setting-sun eye phenomenon
HP:0012471	Thick vermilion border
HP:0012472	Eclabion
HP:0012473	Tongue atrophy
HP:0012474	Carotid artery occlusion
HP:0012475	Decreased circulating level of specific antibody
HP:0012476	Specific pneumococcal antibody deficiency
HP:0012477	Vocal tremor
HP:0012478	Temporomandibular joint ankylosis
HP:0012479	Temporomandibular joint crepitus
HP:0012480	Abnormality of cerebral veins
HP:0012481	Cerebral venous angioma
HP:0012482	Frontal venous angioma
HP:0012483	Abnormal alpha granules
HP:0012484	Abnormal dense granules
HP:0012485	Abnormal surface-connected open canalicular system
HP:0012486	Myelitis
HP:0012487	Cerebellopontine angle arachnoid cyst
HP:0012488	Intraventricular arachnoid cyst
HP:0012489	Suprasellar arachnoid cyst
HP:0012490	Panniculitis
HP:0012491	Abnormal dense tubular system
HP:0012492	Cerebral artery stenosis
HP:0012493	Middle cerebral artery stenosis
HP:0012494	Anterior cerebral artery stenosis
HP:0012495	Posterior cerebral artery stenosis
HP:0012496	Reduced maximal inspiratory pressure
HP:0012497	Reduced maximal expiratory pressure
HP:0012498	Nuchal cord
HP:0012499	Descending aortic dissection
HP:0012500	Verrucous papule
HP:0012501	Abnormality of the brainstem white matter
HP:0012502	Abnormality of the internal capsule
HP:0012503	Abnormality of the pituitary gland
HP:0012504	Abnormal size of pituitary gland
HP:0012505	Enlarged pituitary gland
HP:0012506	Small pituitary gland
HP:0012507	Weakness of orbicularis oculi muscle
HP:0012508	Metamorphopsia
HP:0012509	Reduced thyroxin-binding globulin
HP:0012510	Extra-axial cerebrospinal fluid accumulation
HP:0012511	Temporal optic disc pallor
HP:0012512	Diffuse optic disc pallor
HP:0012513	Upper limb pain
HP:0012514	Lower limb pain
HP:0012515	Hip flexor weakness
HP:0012516	Tetralogy of Fallot with pulmonary atresia
HP:0012517	Reduced catalase activity
HP:0012518	Abnormal circle of Willis morphology
HP:0012519	Hypoplastic posterior communicating artery
HP:0012520	Perivascular spaces
HP:0012521	Optic nerve aplasia
HP:0012522	Spider hemangioma
HP:0012523	Oral aversion
HP:0012524	Abnormal platelet shape
HP:0012525	Abnormal alpha granule distribution
HP:0012526	Absence of alpha granules
HP:0012527	Abnormal alpha granule content
HP:0012528	Abnormal number of alpha granules
HP:0012529	Abnormal dense granule content
HP:0012530	Abnormal number of dense granules
HP:0012531	Pain
HP:0012532	Chronic pain
HP:0012533	Allodynia
HP:0012534	Dysesthesia
HP:0012535	Abnormal synaptic transmission
HP:0012536	Maternal anticardiolipin antibody positive
HP:0012537	Food intolerance
HP:0012538	Gluten intolerance
HP:0012539	Non-Hodgkin lymphoma
HP:0012540	Axillary epidermoid cyst
HP:0012541	Cephalohematoma
HP:0012542	Onychauxis
HP:0012543	Hemosiderinuria
HP:0012544	Elevated aldolase level
HP:0012545	Reduced aldolase level
HP:0012546	Skewed maternal X inactivation
HP:0012547	Abnormal involuntary eye movements
HP:0012548	Fatty replacement of skeletal muscle
HP:0012549	Conjunctival lipoma
HP:0012550	Colonic varices
HP:0012551	Absent neutrophil specific granules
HP:0012552	Increased neutrophil nuclear projections
HP:0012553	Hypoplastic thumbnail
HP:0012554	Absent thumbnail
HP:0012555	Absent nail of hallux
HP:0012556	Hyperbetaalaninemia
HP:0012557	EEG with centrotemporal focal spike waves
HP:0012558	Abnormal T3/T4 ratio
HP:0012559	Increased T3/T4 ratio
HP:0012560	Decreased T3/T4 ratio
HP:0012561	Unicuspid aortic valve
HP:0012562	Premature epimetaphyseal fusion in hand
HP:0012563	Premature epimetaphyseal fusion in foot
HP:0012564	Premature epimetaphyseal fusion in tibia
HP:0012565	Premature epimetaphyseal fusion in fibula
HP:0012566	Premature epimetaphyseal fusion in radius
HP:0012567	Premature epimetaphyseal fusion in ulna
HP:0012568	Lower eyelid edema
HP:0012569	Delayed menarche
HP:0012570	Synovial sarcoma
HP:0012571	Ureter fissus
HP:0012572	Ureter duplex
HP:0012573	Global proximal tubulopathy
HP:0012574	Mesangial hypercellularity
HP:0012575	Abnormality of the nephron
HP:0012576	Glomerular C3 deposition
HP:0012577	Thin glomerular basement membrane
HP:0012578	Membranous nephropathy
HP:0012579	Minimal change glomerulonephritis
HP:0012580	Calcium phosphate nephrolithiasis
HP:0012581	Solitary renal cyst
HP:0012582	Bilateral renal dysplasia
HP:0012583	Unilateral renal hypoplasia
HP:0012584	Bilateral renal hypoplasia
HP:0012585	Renal atrophy
HP:0012586	Bilateral renal atrophy
HP:0012587	Macroscopic hematuria
HP:0012588	Steroid-resistant nephrotic syndrome
HP:0012589	Multidrug-resistant nephrotic syndrome
HP:0012590	Abnormal urine output
HP:0012591	Abnormal urinary electrolyte concentration
HP:0012592	Albuminuria
HP:0012593	Nephrotic range proteinuria
HP:0012594	Microalbuminuria
HP:0012595	Mild proteinuria
HP:0012596	Moderate proteinuria
HP:0012597	Heavy proteinuria
HP:0012598	Abnormal urine potassium concentration
HP:0012599	Abnormal urine phosphate concentration
HP:0012600	Abnormal urine chloride concentration
HP:0012601	Hypochloriduria
HP:0012602	Renal chloride wasting
HP:0012603	Abnormal urine sodium concentration
HP:0012604	Hyponatriuria
HP:0012605	Hypernatriuria
HP:0012606	Renal sodium wasting
HP:0012607	Abnormal urine magnesium concentration
HP:0012608	Hypermagnesiuria
HP:0012609	Hypomagnesiuria
HP:0012610	Abnormality of urinary uric acid concentration
HP:0012611	Increased urinary urate
HP:0012612	Abnormal urinary sulfate concentration
HP:0012613	Increased urinary sulfate
HP:0012614	Abnormal urine cytology
HP:0012615	Cylindruria
HP:0012616	Leukocyte cylindruria
HP:0012617	Erythrocyte cylindruria
HP:0012618	Urachal cyst
HP:0012619	Multiple bladder diverticula
HP:0012620	Cloacal abnormality
HP:0012621	Persistent cloaca
HP:0012622	Chronic kidney disease
HP:0012623	Stage 1 chronic kidney disease
HP:0012624	Stage 2 chronic kidney disease
HP:0012625	Stage 3 chronic kidney disease
HP:0012626	Stage 4 chronic kidney disease
HP:0012627	Pseudoexfoliation
HP:0012628	Abnormal suspensory ligament of lens morphology
HP:0012629	Phakodonesis
HP:0012630	Abnormal trabecular meshwork morphology
HP:0012631	Pigment deposition in the trabecular meshwork
HP:0012632	Abnormal intraocular pressure
HP:0012633	Asymmetry of intraocular pressure
HP:0012634	Iris pigment dispersion
HP:0012635	Iris hypoperfusion
HP:0012636	Retinal vein occlusion
HP:0012637	Renal calcium wasting
HP:0012638	Abnormality of nervous system physiology
HP:0012639	Abnormality of nervous system morphology
HP:0012640	Abnormality of intracranial pressure
HP:0012641	Decreased intracranial pressure
HP:0012642	Cerebellar agenesis
HP:0012643	Foveal hypopigmentation
HP:0012644	Increased caudate lactate level
HP:0012645	Enlarged peripheral nerve
HP:0012646	Retractile testis
HP:0012647	Abnormal inflammatory response
HP:0012648	Decreased inflammatory response
HP:0012649	Increased inflammatory response
HP:0012650	Perisylvian polymicrogyria
HP:0012651	Abasia
HP:0012652	Exercise-induced asthma
HP:0012653	Status asthmaticus
HP:0012654	Abnormal CSF dopamine level
HP:0012655	Elevated CSF dopamine level
HP:0012656	Reduced CSF dopamine level
HP:0012657	Abnormal brain positron emission tomography
HP:0012658	Abnormal brain FDG positron emission tomography
HP:0012659	Prefrontal hypometabolism in FDG PET
HP:0012660	Thalamic hypometabolism in FDG PET
HP:0012661	Hypothalamic hypometabolism in FDG PET
HP:0012662	Parietal hypometabolism in FDG PET
HP:0012663	Mildly reduced ejection fraction
HP:0012664	Reduced ejection fraction
HP:0012665	Moderately reduced ejection fraction
HP:0012666	Severely reduced ejection fraction
HP:0012667	Regional left ventricular wall motion abnormality
HP:0012668	Vasovagal syncope
HP:0012669	Carotid sinus syncope
HP:0012670	Orthostatic syncope
HP:0012671	Abulia
HP:0012672	Akinetic mutism
HP:0012673	Aplasia of the upper vagina
HP:0012674	Aplasia of the lower vagina
HP:0012675	Iron accumulation in brain
HP:0012676	Copper accumulation in brain
HP:0012677	Iron accumulation in globus pallidus
HP:0012678	Iron accumulation in substantia nigra
HP:0012679	Widened interpedicular distance
HP:0012680	Abnormality of the pineal gland
HP:0012681	Abnormality of pineal morphology
HP:0012682	Pineal gland calcification
HP:0012683	Pineal cyst
HP:0012684	Abnormal pineal volume
HP:0012685	Decreased pineal volume
HP:0012686	Increased pineal volume
HP:0012687	Agenesis of pineal gland
HP:0012688	Abnormality of pineal physiology
HP:0012689	Abnormal pineal melatonin secretion
HP:0012690	T2 hypointense thalamus
HP:0012691	Focal T2 hypointense thalamic lesion
HP:0012692	Focal T2 hyperintense thalamic lesion
HP:0012693	Abnormal thalamic size
HP:0012694	Enlarged thalamic volume
HP:0012695	Decreased thalamic volume
HP:0012696	Abnormal thalamic MRI signal intensity
HP:0012697	Small basal ganglia
HP:0012698	Cerebellar gliosis
HP:0012699	Anomaly of lower limb diaphyses
HP:0012700	Abnormal large intestine physiology
HP:0012701	Bowel urgency
HP:0012702	Tenesmus
HP:0012703	Abnormality of the subarachnoid space
HP:0012704	Widened subarachnoid space
HP:0012705	Abnormal metabolic brain imaging by MRS
HP:0012706	Elevated brain choline level by MRS
HP:0012707	Elevated brain lactate level by MRS
HP:0012708	Reduced brain N-acetyl aspartate level by MRS
HP:0012709	Abnormal brain choline/creatine ratio by MRS
HP:0012710	Ingrown nail
HP:0012711	Delayed ossification of vertebral epiphysis
HP:0012712	Mild hearing impairment
HP:0012713	Moderate hearing impairment
HP:0012714	Severe hearing impairment
HP:0012715	Profound hearing impairment
HP:0012716	Moderate conductive hearing impairment
HP:0012717	Severe conductive hearing impairment
HP:0012718	Morphological abnormality of the gastrointestinal tract
HP:0012719	Functional abnormality of the gastrointestinal tract
HP:0012720	Neoplasm of the nose
HP:0012721	Venous malformation
HP:0012722	Heart block
HP:0012723	Sinoatrial block
HP:0012724	Upper eyelid edema
HP:0012725	Cutaneous syndactyly
HP:0012726	Episodic hypokalemia
HP:0012727	Thoracic aortic aneurysm
HP:0012728	Fusiform descending thoracic aortic aneurysm
HP:0012729	Saccular descending thoracic aortic aneurysm
HP:0012730	Aglossia
HP:0012731	Ectopic anterior pituitary gland
HP:0012732	Anorectal anomaly
HP:0012733	Macule
HP:0012734	Ketotic hypoglycemia
HP:0012735	Cough
HP:0012736	Profound global developmental delay
HP:0012737	Small intestinal polyp
HP:0012738	Agenesis of canine
HP:0012739	Agenesis of the small intestine
HP:0012740	Papilloma
HP:0012741	Unilateral cryptorchidism
HP:0012742	Thin fingernail
HP:0012743	Abdominal obesity
HP:0012744	Femoral aplasia
HP:0012745	Short palpebral fissure
HP:0012746	Thin toenail
HP:0012747	Abnormal brainstem MRI signal intensity
HP:0012748	Focal T2 hyperintense brainstem lesion
HP:0012749	Focal T2 hypointense brainstem lesion
HP:0012750	T2 hypointense brainstem
HP:0012751	Abnormal basal ganglia MRI signal intensity
HP:0012752	Focal T2 hypointense basal ganglia lesion
HP:0012753	T2 hypointense basal ganglia
HP:0012754	CNS hypermyelination
HP:0012755	Enlarged brainstem
HP:0012756	CSF polymorphonuclear pleocytosis
HP:0012757	Abnormal neuron morphology
HP:0012758	Neurodevelopmental delay
HP:0012759	Neurodevelopmental abnormality
HP:0012760	Impaired social reciprocity
HP:0012761	Absent mastoid
HP:0012762	Cerebral white matter atrophy
HP:0012763	Paroxysmal dyspnea
HP:0012764	Orthopnea
HP:0012765	Widened cerebellar subarachnoid space
HP:0012766	Widened cerebral subarachnoid space
HP:0012767	Abnormal placental size
HP:0012768	Neonatal asphyxia
HP:0012769	Abnormal arm span
HP:0012770	Reduced arm span
HP:0012771	Increased arm span
HP:0012772	Abnormal upper to lower segment ratio
HP:0012773	Reduced upper to lower segment ratio
HP:0012774	Increased upper to lower segment ratio
HP:0012775	Stellate iris
HP:0012776	Abnormal ciliary body morphology
HP:0012777	Retinal neoplasm
HP:0012778	Retinal astrocytic hamartoma
HP:0012779	Transient hearing impairment
HP:0012780	Neoplasm of the ear
HP:0012781	Mid-frequency hearing loss
HP:0012782	Perilobar nephrogenic rest
HP:0012783	Intralobar nephrogenic rest
HP:0012784	Perinephritis
HP:0012785	Flexion contracture of finger
HP:0012786	Recurrent cystitis
HP:0012787	Recurrent pyelonephritis
HP:0012788	Reticulate pigmentation of oral mucosa
HP:0012789	Hypoplasia of the calcaneus
HP:0012790	Abnormal intramembranous ossification
HP:0012791	Abnormal humeral ossification
HP:0012792	Absent ossification of thoracic vertebral bodies
HP:0012793	Kinked brainstem
HP:0012794	Periventricular white matter hypodensities
HP:0012795	Abnormality of the optic disc
HP:0012796	Increased cup-to-disc ratio
HP:0012797	Lymphatic vessel neoplasm
HP:0012798	Pulmonary lymphangiomyomatosis
HP:0012799	Unilateral facial palsy
HP:0012800	Accessory cranial suture
HP:0012801	Narrow jaw
HP:0012802	Broad jaw
HP:0012803	Anisometropia
HP:0012804	Corneal ulceration
HP:0012805	Iris transillumination defect
HP:0012806	Proboscis
HP:0012807	High insertion of columella
HP:0012808	Abnormal nasal base
HP:0012809	Narrow nasal base
HP:0012810	Wide nasal base
HP:0012811	Wide nasal ridge
HP:0012812	Fullness of paranasal tissue
HP:0012813	Unilateral breast hypoplasia
HP:0012814	Bilateral breast hypoplasia
HP:0012815	Hypoplastic female external genitalia
HP:0012816	Right ventricular noncompaction cardiomyopathy
HP:0012817	Noncompaction cardiomyopathy
HP:0012818	Biventricular noncompaction cardiomyopathy
HP:0012819	Myocarditis
HP:0012820	Bilateral vocal cord paralysis
HP:0012821	Unilateral vocal cord paresis
HP:0012822	Bilateral vocal cord paresis
HP:0012823	Clinical modifier
HP:0012824	Severity
HP:0012825	Mild
HP:0012826	Moderate
HP:0012827	Borderline
HP:0012828	Severe
HP:0012829	Profound
HP:0012830	Position
HP:0012831	Laterality
HP:0012832	Bilateral
HP:0012833	Unilateral
HP:0012834	Right
HP:0012835	Left
HP:0012836	Spatial pattern
HP:0012837	Generalized
HP:0012838	Localized
HP:0012839	Distal
HP:0012840	Proximal
HP:0012841	Retinal vascular tortuosity
HP:0012842	Skin appendage neoplasm
HP:0012843	Hair follicle neoplasm
HP:0012844	Trichilemmoma
HP:0012845	Single trichilemmoma
HP:0012846	Multiple trichilemmomata
HP:0012847	Epilepsia partialis continua
HP:0012848	Small intestinal stenosis
HP:0012849	Small intestinal bleeding
HP:0012850	Small intestinal dysmotility
HP:0012851	Colonic stenosis
HP:0012852	Hepatic bridging fibrosis
HP:0012853	Scrotal hypospadias
HP:0012854	Midshaft hypospadias
HP:0012855	Scrotal hyperpigmentation
HP:0012856	Abnormal scrotal rugation
HP:0012857	Increased scrotal rugation
HP:0012858	Decreased scrotal rugation
HP:0012859	Esophageal leukoplakia
HP:0012860	Testicular fibrosis
HP:0012861	Ovotestis
HP:0012862	Abnormal germ cell morphology
HP:0012863	Abnormal male germ cell morphology
HP:0012864	Abnormal sperm morphology
HP:0012865	Sperm head anomaly
HP:0012866	Sperm neck anomaly
HP:0012867	Sperm mid-piece anomaly
HP:0012868	Sperm tail anomaly
HP:0012869	Acephalic spermatozoa
HP:0012870	Vanishing testis
HP:0012871	Varicocele
HP:0012872	Abnormal vas deferens morphology
HP:0012873	Absent vas deferens
HP:0012874	Abnormal male reproductive system physiology
HP:0012875	Abnormal ejaculation
HP:0012876	Premature ejaculation
HP:0012877	Retrograde ejaculation
HP:0012878	Retarded ejaculation
HP:0012879	Anejaculation
HP:0012880	Abnormality of the labia minora
HP:0012881	Abnormality of the labia majora
HP:0012882	Hyperplastic labia majora
HP:0012883	Fallopian tube cyst
HP:0012884	Fallopian tube torsion
HP:0012885	Fallopian tube duplication
HP:0012886	Hemorrhagic ovarian cyst
HP:0012887	Ovarian serous cystadenoma
HP:0012888	Abnormality of the uterine cervix
HP:0012889	Cervical endometriosis
HP:0012890	Posteriorly placed anus
HP:0012891	High posterior hairline
HP:0012892	Facial muscle hypertrophy
HP:0012893	Neck muscle hypertrophy
HP:0012894	Paraspinal muscle hypertrophy
HP:0012895	Scapular muscle hypertrophy
HP:0012896	Abnormal motor evoked potentials
HP:0012897	Abnormal upper-limb motor evoked potentials
HP:0012898	Abnormal lower-limb motor evoked potentials
HP:0012899	Handgrip myotonia
HP:0012900	Myotonia of the face
HP:0012901	Myotonia of the jaw
HP:0012902	Myotonia of the lower limb
HP:0012903	Myotonia of the upper limb
HP:0012904	Cold-sensitive myotonia
HP:0012905	Euryblepharon
HP:0020006	Ciliary body coloboma
HP:0020034	Diffuse
HP:0020035	Lower limb dysmetria
HP:0020036	Upper limb dysmetria
HP:0020037	Astasia
HP:0020038	Vertebrobasilar dolichoectasia
HP:0020041	Double elevator palsy
HP:0020042	Double depressor palsy
HP:0020043	Vertical incomitant strabismus
HP:0020044	Horizontal incomitant strabismus
HP:0020045	Esodeviation
HP:0020046	Accommodative esotropia
HP:0020047	Abnormal myeloid cell morphology
HP:0020048	Reduced bone-marrow pro-B cell count
HP:0020049	Exodeviation
HP:0020050	Anti-granulocyte-macrophage colony stimulating factor antibody positivity
HP:0020054	Abnormal erythrocyte physiology
HP:0020058	Abnormal red blood cell count
HP:0020059	Increased red blood cell count
HP:0020060	Decreased red blood cell count
HP:0020061	Abnormal hemoglobin concentration
HP:0020062	Decreased hemoglobin concentration
HP:0020063	Increased hemoglobin concentration
HP:0020064	Abnormal eosinophil count
HP:0025004	Hallux rigidus
HP:0025005	Thickening of glomerular capillary wall
HP:0025006	Abnormal glomerular capillary morphology
HP:0025007	Ectopic fovea
HP:0025008	Tracheal tug on inspiration
HP:0025009	Forward slanting upper incisors
HP:0025010	Foveal atrophy
HP:0025011	Pyriform aperture stenosis
HP:0025012	Status cribrosum
HP:0025013	Decerebrate rigidity
HP:0025014	Subcutaneous spheroids
HP:0025015	Abnormal vascular morphology
HP:0025016	Abnormal capillary morphology
HP:0025017	Capillary fragility
HP:0025018	Abnormal capillary physiology
HP:0025019	Arterial rupture
HP:0025020	Elevated prostate-specific antigen level
HP:0025021	Abnormal erythrocyte sedimentation rate
HP:0025022	Decreased erythrocyte sedimentation rate
HP:0025023	Rectal atresia
HP:0025024	Megarectum
HP:0025025	Rectovestibular fistula
HP:0025026	H-type rectovestibular fistula
HP:0025027	Osteoma cutis
HP:0025028	Abnormality of enteric nervous system morphology
HP:0025029	Abnormality of enteric neuron morphology
HP:0025030	Enteric neuronal degeneration
HP:0025031	Abnormality of the digestive system
HP:0025032	Abnormality of digestive system physiology
HP:0025033	Abnormality of digestive system morphology
HP:0025034	Abnormal morphology of erythroid progenitor cell
HP:0025035	Abnormal proerythroblast morphology
HP:0025037	Hypothalamic gliosis
HP:0025038	Intratesticular abscess
HP:0025039	Basal ganglia edema
HP:0025040	Thalamic edema
HP:0025041	Thalamic calcification
HP:0025042	Abnormality of mesenteric lymph nodes
HP:0025043	Enlarged mesenteric lymph node
HP:0025044	Lung abscess
HP:0025045	Abnormal brain lactate level by MRS
HP:0025046	Reduced brain lactate level by MRS
HP:0025047	Abnormal brain choline level by MRS
HP:0025048	Reduced brain choline level by MRS
HP:0025049	Abnormal brain creatine level by MRS
HP:0025050	Elevated brain creatine level by MRS
HP:0025051	Reduced brain creatine level by MRS
HP:0025052	Abnormal brain N-acetyl aspartate level by MRS
HP:0025053	Elevated brain N-acetyl aspartate level by MRS
HP:0025057	Abnormality of olfactory lobe morphology
HP:0025058	Hypothalamic atrophy
HP:0025059	Splenic abscess
HP:0025060	Multifocal splenic abscess
HP:0025061	Unifocal splenic abscess
HP:0025062	Geophagia
HP:0025063	Scaphoid abdomen
HP:0025064	Thalamic hemorrhage
HP:0025065	Abnormal mean corpuscular volume
HP:0025066	Decreased mean corpuscular volume
HP:0025068	Incomitant strabismus
HP:0025069	Concomitant strabismus
HP:0025070	Abnormal U wave
HP:0025071	U wave inversion
HP:0025072	Prominent U wave
HP:0025073	Exercise-induced U wave inversion
HP:0025074	Abnormal QRS complex
HP:0025075	Increased QRS voltage
HP:0025076	Abnormal QRS voltage
HP:0025077	Decreased QRS voltage
HP:0025078	Electrical alternans
HP:0025079	Pancreatic abscess
HP:0025080	Orthokeratotic hyperkeratosis
HP:0025081	Darier's sign
HP:0025082	Abnormal cutaneous elastic fiber morphology
HP:0025083	Elevated dermal desmosine content
HP:0025084	Folliculitis
HP:0025085	Bloody diarrhea
HP:0025086	Bloody mucoid diarrhea
HP:0025087	Delayed recoil upon stretching of skin
HP:0025088	Onychomadesis
HP:0025089	Feculent vomiting
HP:0025090	Abnormal large intestinal mucosa morphology
HP:0025092	Epidermal acanthosis
HP:0025093	Peripapillary exudate
HP:0025094	Disciform macular scar
HP:0025095	Sneeze
HP:0025096	Paroxysmal sneezing
HP:0025097	Eyelid myoclonus
HP:0025098	Dysgenesis of the hypothalamus
HP:0025099	Dysgenesis of the thalamus
HP:0025100	Abnormal morphology of the hippocampus
HP:0025101	Dysgenesis of the hippocampus
HP:0025102	Dysgenesis of the basal ganglia
HP:0025103	Umbilicated nodule
HP:0025104	Capillary malformation
HP:0025105	Nevus anemicus
HP:0025106	Nevus roseus
HP:0025107	Cutis marmorata telangiectatica congenita
HP:0025108	Angioma serpentinum
HP:0025109	Reduced red cell pyruvate kinase activity
HP:0025110	Placoid macular lesion
HP:0025112	Sound sensitivity
HP:0025113	Misophonia
HP:0025114	Hypergranulosis
HP:0025115	Civatte bodies
HP:0025116	Fetal distress
HP:0025117	Rete ridge flattening
HP:0025118	Lip discoloration
HP:0025119	Violet lip discoloration
HP:0025121	Simple partial occipital seizures
HP:0025122	Sawtooth acanthosis
HP:0025123	White streaks/specks on enamel.
HP:0025124	Fragile teeth
HP:0025125	White lesion of the oral mucosa
HP:0025126	Oral hairy leukoplakia
HP:0025127	Actinic keratosis
HP:0025128	Reduced intraabdominal adipose tissue
HP:0025129	Abnormal small intestinal mucosa morphology
HP:0025130	Decreased small intestinal mucosa lactase activity
HP:0025131	Finger swelling
HP:0025132	Abnormal circulating estrogen level
HP:0025133	Abnormal serum estradiol
HP:0025134	Increased serum estradiol
HP:0025135	Abnormal serum estriol
HP:0025136	Increased serum estriol
HP:0025137	Decreased serum estriol
HP:0025138	Abnormal serum estrone
HP:0025139	Increased serum estrone
HP:0025140	Decreased serum estrone
HP:0025141	Gingival calcification
HP:0025142	Constitutional symptom
HP:0025143	Chills
HP:0025144	Shivering
HP:0025145	Rigors
HP:0025146	Foveal degeneration
HP:0025147	Beaten bronze macular sheen
HP:0025148	Dark choroid
HP:0025149	Atrophic muscularis propria
HP:0025150	Hypoganglionosis
HP:0025151	Ganglioneuromatosis
HP:0025152	Poor visual behavior for age
HP:0025153	Transient
HP:0025154	Portosystemic collateral veins
HP:0025155	Abnormality of hepatobiliary system physiology
HP:0025156	Dependency on intravenous nutrition
HP:0025157	Increased urinary sedoheptulose
HP:0025158	Hyperautofluorescent retinal lesion
HP:0025159	Hypoautofluorescent retinal lesion
HP:0025160	Abnormal temper tantrums
HP:0025161	Frequent temper tantrums
HP:0025162	Severe temper tantrums
HP:0025163	Abnormality of optic chiasm morphology
HP:0025164	Increased number of elastic fibers in the dermis
HP:0025165	Clumping of elastic fibers in the dermis
HP:0025166	Thickened elastic fibers in the dermis
HP:0025167	Fragmented elastic fibers in the dermis
HP:0025168	Left ventricular diastolic dysfunction
HP:0025169	Left ventricular systolic dysfunction
HP:0025170	Neuronal/glioneuronal neoplasm of the central nervous system
HP:0025171	Rosette-forming glioneuronal tumor
HP:0025172	Smooth septal thickening on pulmonary HRCT
HP:0025173	Nodular septal thickening on pulmonary HRCT
HP:0025174	Irregular septal thickening on pulmonary HRCT
HP:0025175	Honeycomb lung
HP:0025176	Intralobular interstitial thickening
HP:0025177	Peribronchovascular interstitial thickening
HP:0025178	Subpleural interstitial thickening
HP:0025179	Ground-glass opacification on pulmonary HRCT
HP:0025180	Centrilobular ground-glass opacification on pulmonary HRCT
HP:0025181	Abdominal aseptic abscess
HP:0025182	Localized area of pendulous skin
HP:0025186	Marcus Gunn jaw winking synkinesis
HP:0025188	Retinal vasculitis
HP:0025190	Generalized tonic-clonic seizures without focal onset
HP:0025191	Segmental myoclonic seizures
HP:0025192	Subtentorial periventricular white matter hyperdensity
HP:0025193	Posterolateral diaphragmatic hernia
HP:0025194	Morgagni diaphragmatic hernia
HP:0025195	Central diaphragmatic hernia
HP:0025196	Increased total iron binding capacity
HP:0025197	Inclusion body fibromatosis
HP:0025198	Inflammatory cap polyp
HP:0025200	Muscle fiber actin filament accumulation
HP:0025201	Abnormal apolipoprotein level
HP:0025202	Elevated apolipoprotein A-IV level
HP:0025203	Caput medusae
HP:0025204	Triggered by
HP:0025205	Triggered by breast feeding
HP:0025206	Triggered by cold
HP:0025207	Triggered by dehydration
HP:0025208	Triggered by carbohydrate ingestion
HP:0025209	Triggered by fructose ingestion
HP:0025210	Triggered by glucose ingestion
HP:0025211	Triggered by ethanol ingestion
HP:0025212	Triggered by fasting
HP:0025213	Triggered by galactose ingestion
HP:0025214	Triggered by heat
HP:0025215	Triggered by febrile illness
HP:0025216	Triggered by heavy meal
HP:0025217	Triggered by high-fat diet
HP:0025218	Triggered by hyperventilation
HP:0025219	Triggered by vaccination
HP:0025220	Triggered by menstruation
HP:0025221	Triggered by pregnancy
HP:0025222	Triggered by sleep deprivation
HP:0025223	Triggered by smoking
HP:0025224	Triggered by sodium ingestion
HP:0025225	Triggered by sound
HP:0025226	Triggered by stress
HP:0025227	Triggered by excitement
HP:0025228	Triggered by sudden movement
HP:0025229	Triggered by vestibular stimulation
HP:0025230	Tendonitis
HP:0025231	Abnormality of synovial bursa morphology
HP:0025232	Bursitis
HP:0025233	Sleep paralysis
HP:0025234	Parasomnia
HP:0025235	Non-rapid eye movement parasomnia
HP:0025236	Somnambulism
HP:0025237	Confusional arousal
HP:0025238	Foot pain
HP:0025239	Subhyaloid hemorrhage
HP:0025240	Preretinal hemorrhage
HP:0025241	Flame-shaped retinal hemorrhage
HP:0025242	Dot-and-blot retinal hemorrhage
HP:0025243	Subretinal hemorrhage
HP:0025244	Subretinal pigment epithelium hemorrhage
HP:0025245	Cutaneous cyst
HP:0025246	Trichilemmal cyst
HP:0025247	Dermoid cyst
HP:0025248	Eruptive vellus hair cyst
HP:0025249	Comedo
HP:0025250	Closed comedo
HP:0025251	Open comedo
HP:0025252	Geographic tongue
HP:0025253	Claustrophobia
HP:0025254	Ameliorated by
HP:0025255	Ameliorated by pregnancy
HP:0025256	Ameliorated by heat
HP:0025257	Ameliorated by carbohydrate ingestion
HP:0025258	Stiff neck
HP:0025259	Stiff elbow
HP:0025260	Stiff wrist
HP:0025261	Stiff finger
HP:0025262	Stiff hip
HP:0025263	Stiff knee
HP:0025264	Stiff ankle
HP:0025265	Stiff toe
HP:0025266	Cervical osteoarthritis
HP:0025267	Snoring
HP:0025268	Stuttering
HP:0025269	Panic attack
HP:0025270	Abnormality of esophagus physiology
HP:0025271	Esophageal spasms
HP:0025272	Melasma
HP:0025273	Achilles tendonitis
HP:0025274	Ovarian dermoid cyst
HP:0025275	Lateral
HP:0025276	Abnormality of skin adnexa physiology
HP:0025277	Gustatory sweating
HP:0025278	Cold-induced sweating
HP:0025279	Migratory
HP:0025280	Pain characteristic
HP:0025281	Sharp
HP:0025282	Dull
HP:0025283	Tender
HP:0025284	Sleep-interrupting
HP:0025285	Aggravated by
HP:0025286	Aggravated by activity
HP:0025287	Axial
HP:0025289	Cervical lymphadenopathy
HP:0025290	Upper-body predominance
HP:0025291	Lower-body predominance
HP:0025292	Acral
HP:0025293	Distributed along Blashko lines
HP:0025294	Dermatomal
HP:0025295	Herpetiform
HP:0025296	Morbilliform
HP:0025297	Prolonged
HP:0025300	Malar rash
HP:0025301	Nocturnal
HP:0025302	Diurnal
HP:0025303	Episodic
HP:0025304	Periodic
HP:0025305	Quotidian
HP:0025306	Acute emergence over minutes
HP:0025307	Acute emergence over hours
HP:0025308	Acute emergence over days
HP:0025309	Abnormal pupil shape
HP:0025310	Oval pupil
HP:0025311	Anterior chamber cyst
HP:0025312	Esophoria
HP:0025313	Exophoria
HP:0025314	Choroidal nevus
HP:0025315	Exacerbated by head trauma
HP:0025317	Cubitus varus
HP:0025318	Ovarian carcinoma
HP:0025319	Rubeosis iridis
HP:0025320	Leakage of dye on fundus fluorescein angiography
HP:0025321	Copper accumulation in liver
HP:0025322	Venous occlusion
HP:0025323	Abnormal arterial physiology
HP:0025324	Arterial occlusion
HP:0025325	Sparse medial eyebrow
HP:0025326	Retinal arterial occlusion
HP:0025327	Decreased renal parenchymal thickness
HP:0025328	Antepartum hemorrhage
HP:0025329	Anti-glutamic acid decarboxylase antibody positivity
HP:0025330	Downgaze palsy
HP:0025331	Upgaze palsy
HP:0025332	Abnormality of foot cortical bone
HP:0025333	Cortical thinning of foot bones
HP:0025334	Triggered by emotion
HP:0025335	Delayed ability to stand
HP:0025336	Delayed ability to sit
HP:0025337	Red eye
HP:0025338	Circumlimbal hyperemia
HP:0025339	Superficial episcleral hyperemia
HP:0025340	Deep episcleral hyperemia
HP:0025341	Corneal keratic precipitates
HP:0025342	Central retinal artery occlusion
HP:0025343	Lupus anticoagulant
HP:0025344	Interlobular bile duct destruction
HP:0025345	Abnormality of circulating beta-2-microglobulin level
HP:0025346	Increased circulating beta-2-microglobulin level
HP:0025347	Decreased circulating beta-2-microglobulin level
HP:0025348	Abnormality of the corneal limbus
HP:0025349	Limbal edema
HP:0025350	Giant conjunctival papillae
HP:0025351	Recurrent interdigital mycosis
HP:0025352	Autosomal dominant germline de novo mutation
HP:0025353	Anti-multiple nuclear dots antibody positivity
HP:0025354	Abnormal cellular phenotype
HP:0025355	Retinal arterial macroaneurysms
HP:0025356	Psychomotor retardation
HP:0025357	Erratic myoclonus
HP:0025358	Uveal ectropion
HP:0025359	Polygonal renal calices
HP:0025360	Polycalycosis
HP:0025361	Abnormality of medullary pyramid morphology
HP:0025362	Renal medullary pyramid hypoplasia
HP:0025363	Endocapillary hypercellularity
HP:0025364	Extracapillary hypercellularity
HP:0025367	Trichoepithelioma
HP:0025368	Abnormality of growth plate morphology
HP:0025369	Thick growth plates
HP:0025370	Abnormal ossification of the sacrum
HP:0025371	Delayed ossification of the sacrum
HP:0025372	Loud snoring
HP:0025373	Interictal EEG abnormality
HP:0025374	Duplicated odontoid process
HP:0025375	Orthotopic os odontoideum
HP:0025376	Hyperglutaminuria
HP:0025377	Triggered by exertion
HP:0025379	Anti-thyroid peroxidase antibody positivity
HP:0025380	Increased serum androstenedione
HP:0025381	Anti-pituitary antibody positivity
HP:0025382	Hypodipsia
HP:0025383	Dorsocervical fat pad
HP:0025384	Diet-resistant subcutaneous adipose tissue
HP:0025385	Diet-resistant subcutaneous adipose tissue below waist
HP:0025386	Bitemporal hollowing
HP:0025387	Pill-rolling tremor
HP:0025388	Thyroid nodule
HP:0025389	Pulmonary interstitial high-resolution computed tomography abnormality
HP:0025390	Reticular pattern on pulmonary HRCT
HP:0025391	Crazy paving pattern on pulmonary HRCT
HP:0025392	Nodular pattern on pulmonary HRCT
HP:0025393	Reticulonodular pattern on pulmonary HRCT
HP:0025394	Cystic pattern on pulmonary HRCT
HP:0025395	Combined cystic and ground-glass pattern on pulmonary HRCT
HP:0025396	Decreased attenuation pattern on pulmonary HRCT
HP:0025397	Mosaic attenuation pattern on pulmonary HRCT
HP:0025398	Nodular-perilymphatic pattern on pulmonary HRCT
HP:0025399	Nodular-centrilobular with tree-in-bud pattern on pulmonary HRCT
HP:0025400	Nodular-random pattern on pulmonary HRCT
HP:0025401	Staring gaze
HP:0025402	Square-wave jerks
HP:0025403	Stooped posture
HP:0025404	Abnormal visual fixation
HP:0025405	Visual fixation instability
HP:0025406	Asthenia
HP:0025407	Rectourethral fistula
HP:0025408	Abnormal spleen morphology
HP:0025409	Abnormal spleen physiology
HP:0025410	Splenogonadal fusion
HP:0025413	Fossa navicularis urethral stricture
HP:0025414	Pendulous urethral stricture
HP:0025415	Bulbar urethral stricture
HP:0025416	Vaginal stricture
HP:0025417	Patulous urethra
HP:0025418	Renal cortical necrosis
HP:0025419	Pulmonary pneumatocele
HP:0025420	Diffuse alveolar hemorrhage
HP:0025421	Pneumomediastinum
HP:0025422	Pleural cyst
HP:0025423	Abnormal larynx morphology
HP:0025424	Abnormal larynx physiology
HP:0025425	Laryngospasm
HP:0025426	Abnormal bronchus morphology
HP:0025427	Abnormal bronchus physiology
HP:0025428	Bronchospasm
HP:0025429	Abnormal cry
HP:0025430	High-pitched cry
HP:0025431	Staccato cry
HP:0025432	Acanthoma
HP:0025433	Decreased lecithin cholesterol acyl transferase activity
HP:0025434	Reduced hemolytic complement activity
HP:0025435	Increased lactate dehydrogenase activity
HP:0025436	Elevated serum 11-deoxycortisol
HP:0025437	Macrocephalic sperm head
HP:0025439	Pharyngitis
HP:0025440	Warm reactive autoantibody positivity
HP:0025441	Achilles tendon calcification
HP:0025443	Abnormal cardiac atrial physiology
HP:0025444	Reduced amygdala volume
HP:0025445	Morphological abnormality of the papillary muscles
HP:0025446	Anomalous insertion of papillary muscle directly into anterior mitral leaflet
HP:0025447	Displacement of the papillary muscles
HP:0025448	Anterior displacement of the papillary muscles
HP:0025449	Apically displaced anterolateral papillary muscle
HP:0025451	Testicular adrenal rest tumor
HP:0025452	Pyoderma gangrenosum
HP:0025453	Delayed adrenarche
HP:0025454	Abnormal CSF metabolite level
HP:0025455	Decreased CSF 5-hydroxyindolacetic acid
HP:0025456	Abnormal CSF protein level
HP:0025457	Decreased CSF protein
HP:0025458	Decreased CSF albumin
HP:0025459	Increased CSF/serum albumin ratio
HP:0025460	High myoinositol in brain by MRS
HP:0025461	Abnormal cell morphology
HP:0025462	obsolete Abnormal cellular physiology
HP:0025463	Abnormality of redox activity
HP:0025464	Increased reactive oxygen species production
HP:0025465	Abnormal circulating beta globulin level
HP:0025466	Beta 2-microglobulinuria
HP:0025469	Anagen effluvium
HP:0025470	Telogen effluvium
HP:0025471	Congenital panfollicular nevus
HP:0025472	Recurrent plantar mycosis
HP:0025473	Hyperpigmented papule
HP:0025474	Erythematous plaque
HP:0025475	Erythematous macule
HP:0025476	Testicular lipomatosis
HP:0025477	Periarticular calcification
HP:0025478	Atrial standstill
HP:0025479	Self-neglect
HP:0025480	Lipomyelomeningocele
HP:0025481	Cervical hemivertebrae
HP:0025482	Positive perchlorate discharge test
HP:0025483	Abnormal circulating thyroglobulin level
HP:0025484	Increased circulating thyroglobulin level
HP:0025485	Vaginal adenosis
HP:0025486	Fused labia majora
HP:0025487	Abnormality of bladder morphology
HP:0025488	Detrusor sphincter dyssynergia
HP:0025489	Bladder duplication
HP:0025490	Myocardial bridging
HP:0025491	Venous stenosis
HP:0025492	Microcoria
HP:0025493	Palmoplantar erythema
HP:0025494	Coated aorta
HP:0025495	Descending aorta hypoplasia
HP:0025496	Abnormal coronary artery physiology
HP:0025497	Coronary artery spasm
HP:0025498	Aceruloplasminemia
HP:0025499	Class I obesity
HP:0025500	Class II obesity
HP:0025501	Class III obesity
HP:0025502	Overweight
HP:0025503	Anomalous coronary artery arising from the opposite sinus
HP:0025505	Anomalous origin of the circumflex artery from the right sinus of Valsalva
HP:0025506	Coronary artery sandwich anomaly
HP:0025507	Yellow papule
HP:0025508	Gottron's papules
HP:0025509	Piezogenic pedal papules
HP:0025510	Nevus spillus
HP:0025511	Nevus sebaceus
HP:0025512	Skin-colored papule
HP:0025513	Scleral rupture
HP:0025514	Morning glory anomaly
HP:0025515	Delayed thelarche
HP:0025516	Coronary-pulmonary artery fistula
HP:0025517	Hypoplastic hippocampus
HP:0025518	Visual gaze preference
HP:0025519	Multiple biliary hamartomas
HP:0025520	Calcinosis cutis
HP:0025521	Increased body fat percentage
HP:0025522	Elongated chordae tendinae of the mitral valve
HP:0025523	Abnormal morphology of the chordae tendinae of the mitral valve
HP:0025524	Palmoplantar scaling skin
HP:0025525	Scaling skin on fingertip
HP:0025526	Psoriasiform lesion
HP:0025527	Serpiginous cutaneous lesion
HP:0025528	Annular cutaneous lesion
HP:0025529	Hyperpigmented nodule
HP:0025530	Xanthomas of the palmar creases
HP:0025531	Harlequin phenomenon
HP:0025532	Positive pathergy test
HP:0025533	Peau d'orange
HP:0025534	Ocular melanocytosis
HP:0025535	Shawl sign
HP:0025536	V-sign
HP:0025537	Plantar edema
HP:0025538	Palmar edema
HP:0025539	Abnormal B cell subset distribution
HP:0025540	Abnormal T cell subset distribution
HP:0025541	obsolete Decreased activity of complement receptor
HP:0025546	Abnormal mean corpuscular hemoglobin concentration
HP:0025547	Decreased mean corpuscular hemoglobin concentration
HP:0025548	Increased mean corpuscular hemoglobin concentration
HP:0025549	Eccentric visual fixation
HP:0025550	Elevated circulating ribitol concentration
HP:0025551	Optic nerve misrouting
HP:0025552	Periorbital purpura
HP:0025553	Periorbital ecchymosis with tarsal plate sparing
HP:0025554	Yellow nodule
HP:0025555	Periungual teleangiectasia
HP:0025558	Lamellar cataract with riders
HP:0025559	Coronary cataract
HP:0025560	Anterior chamber cells
HP:0025561	Anterior chamber cells grade 1+
HP:0025562	Anterior chamber cells grade 0.5+
HP:0025563	Anterior chamber cells grade 0
HP:0025564	Anterior chamber cells grade 2+
HP:0025565	Anterior chamber cells grade 3+
HP:0025566	Anterior chamber cells grade 4+
HP:0025567	Central serous chorioretinopathy
HP:0025568	Abnormal morphology of the choroidal vasculature
HP:0025569	Polypoidal choroidal vasculopathy
HP:0025570	Choroidal vascular hyperpermeability
HP:0025571	Christmas tree cataract
HP:0025572	Punctal stenosis
HP:0025573	Mild myopia
HP:0025574	Macular hemorrhage
HP:0025575	Abnormal superior vena cava morphology
HP:0025576	Abnormal inferior vena cava morphology
HP:0025578	Aortic valve prolapse
HP:0025579	Abnormal left atrium morphology
HP:0025580	Abnormal right atrium morphology
HP:0025581	Foveal hemorrhage
HP:0025582	Submacular hemorrhage
HP:0025583	Tapetal-like fundal reflex
HP:0025584	Hypotropia
HP:0025585	Hyperphoria
HP:0025586	Hypertropia
HP:0025587	Hyperdeviation
HP:0025588	Hypodeviation
HP:0025589	Cyclodeviation
HP:0025590	Abnormal extraocular muscle physiology
HP:0025591	Abnormal superior oblique muscle physiology
HP:0025592	Superior oblique muscle weakness
HP:0025593	Superior oblique muscle restriction
HP:0025594	Superior oblique muscle overaction
HP:0025595	Superior oblique muscle underaction
HP:0025596	Abnormal inferior oblique muscle physiology
HP:0025597	Inferior oblique muscle restriction
HP:0025598	Inferior oblique muscle weakness
HP:0025599	Inferior oblique muscle overaction
HP:0025600	Abnormal inferior rectus muscle physiology
HP:0025601	Inferior rectus muscle weakness
HP:0025602	Inferior rectus muscle restriction
HP:0025603	Abnormal superior rectus muscle physiology
HP:0025604	Orbital schwannoma
HP:0025605	Lid lag on downgaze
HP:0025606	Abnormal medial rectus muscle physiology
HP:0025607	Upper eyelid entropion
HP:0025608	Cicatricial ectropion
HP:0025609	Anterior blepharitis
HP:0025610	Posterior blepharitis
HP:0025611	Epicanthus superciliaris
HP:0025612	Corneal astigmatism
HP:0025613	Focal emotional seizure
HP:0030000	EMG: repetitive nerve stimulation abnormality
HP:0030001	Lagopthalmos
HP:0030002	Nocturnal lagophthalmos
HP:0030003	Paralytic lagophthalmos
HP:0030004	Cicatricial lagophthalmos
HP:0030005	Capillary leak
HP:0030006	Single fiber EMG abnormality
HP:0030007	EMG: positive sharp waves
HP:0030008	Cervical agenesis
HP:0030009	Cervical insufficiency
HP:0030010	Hydrometrocolpos
HP:0030011	Imperforate hymen
HP:0030012	Abnormal female reproductive system physiology
HP:0030013	obsolete Endometriosis
HP:0030014	Female sexual dysfunction
HP:0030015	Female anorgasmia
HP:0030016	Dyspareunia
HP:0030017	Vaginismus
HP:0030018	Decreased female libido
HP:0030019	Increased female libido
HP:0030021	Auricular tag
HP:0030022	Question mark ear
HP:0030023	Quelprud nodule
HP:0030024	Pretragal ectopia
HP:0030025	Auricular pit
HP:0030026	Squared superior portion of helix
HP:0030027	Abnormality of the nasal cartilage
HP:0030028	Absent nasal cartilage
HP:0030029	Splayed fingers
HP:0030030	Absent ray
HP:0030031	Small toe
HP:0030032	Partial absence of foot
HP:0030033	Small finger
HP:0030034	Diffuse glomerular basement membrane lamellation
HP:0030035	Struvite nephrolithiasis
HP:0030036	Isothenuria
HP:0030037	Bifid ureter
HP:0030038	Enchondroma
HP:0030039	Fused thoracic vertebrae
HP:0030040	Fused lumbar vertebrae
HP:0030041	Schmorl's node
HP:0030042	Incomplete ossification of pubis
HP:0030043	Hip subluxation
HP:0030044	Flexion contracture of digit
HP:0030045	Serpentine fibula
HP:0030046	Hypoglycosylation of alpha-dystroglycan
HP:0030047	Abnormality of lateral ventricle
HP:0030048	Colpocephaly
HP:0030049	Brain abscess
HP:0030050	Narcolepsy
HP:0030051	Tip-toe gait
HP:0030052	Inguinal freckling
HP:0030053	Stiff skin
HP:0030054	Perifollicular fibrosis
HP:0030055	Hyperconvex toenail
HP:0030056	Uncombable hair
HP:0030057	Autoimmune antibody positivity
HP:0030058	Sickled erythrocytes
HP:0030059	Mitochondrial depletion
HP:0030060	Nervous tissue neoplasm
HP:0030061	Neuroectodermal neoplasm
HP:0030062	Craniopharyngioma
HP:0030063	Neuroepithelial neoplasm
HP:0030064	Neurocytoma
HP:0030065	Primitive neuroectodermal tumor
HP:0030066	Ependymoblastoma
HP:0030067	Peripheral primitive neuroectodermal neoplasm
HP:0030068	Olfactory esthesioneuroblastoma
HP:0030069	Primary central nervous system lymphoma
HP:0030070	Central primitive neuroectodermal tumor
HP:0030071	Medulloepithelioma
HP:0030072	Paranasal sinus neoplasm
HP:0030073	obsolete Pharyngeal neoplasm
HP:0030074	Chemodectoma
HP:0030075	Ductal carcinoma in situ
HP:0030076	Lobular carcinoma in situ
HP:0030077	Bronchial neoplasm
HP:0030078	Lung adenocarcinoma
HP:0030079	Cervix cancer
HP:0030080	Burkitt lymphoma
HP:0030081	Punctate periventricular T2 hyperintense foci
HP:0030082	Abnormal drinking behavior
HP:0030083	Salt craving
HP:0030084	Clinodactyly
HP:0030085	Abnormal CSF lactate level
HP:0030086	Reduced CSF lactate
HP:0030087	Abnormal serum testosterone level
HP:0030088	Increased serum testosterone level
HP:0030089	Abnormal muscle fiber protein expression
HP:0030090	Abnormal muscle fiber merosin expression
HP:0030091	Absent muscle fiber merosin
HP:0030092	Reduced muscle fiber merosin
HP:0030093	Abnormal muscle fiber laminin beta 1
HP:0030094	Reduced muscle fiber laminin beta 1
HP:0030095	Reduced muscle collagen VI
HP:0030096	Abnormal muscle fiber dystrophin expression
HP:0030097	Absent muscle dystrophin expression
HP:0030098	Reduced muscle dystrophin expression
HP:0030099	Reduced muscle fiber alpha dystroglycan
HP:0030100	Abnormal muscle fiber alpha sarcoglycan
HP:0030101	Absent muscle fiber alpha sarcoglycan
HP:0030102	Reduced muscle fiber alpha sarcoglycan
HP:0030103	Abnormal muscle fiber beta sarcoglycan
HP:0030104	Abnormal muscle fiber gamma sarcoglycan
HP:0030105	Abnormal muscle fiber delta sarcoglycan
HP:0030106	Absent muscle fiber beta sarcoglycan
HP:0030107	Reduced muscle fiber beta sarcoglycan
HP:0030108	Reduced muscle fiber gamma sarcoglycan
HP:0030109	Absent muscle fiber gamma sarcoglycan
HP:0030110	Absent muscle fiber delta sarcoglycan
HP:0030111	Reduced muscle fiber delta sarcoglycan
HP:0030112	Abnormal muscle fiber alpha dystroglycan
HP:0030113	Abnormal muscle fiber dysferlin
HP:0030114	Absent muscle fiber dysferlin
HP:0030115	Reduced muscle fiber dysferlin
HP:0030116	Abnormal muscle fiber emerin
HP:0030117	Absent muscle fiber emerin
HP:0030118	Reduced muscle fiber emerin
HP:0030119	Abnormal muscle fiber calpain-3
HP:0030120	Absent muscle fiber calpain-3
HP:0030121	Reduced muscle fiber calpain-3
HP:0030122	Reduced muscle fiber perlecan
HP:0030123	Abnormal muscle fiber lamin A/C
HP:0030124	Reduced muscle fiber lamin A/C
HP:0030125	Sacralization of the fifth lumbar vertebra
HP:0030126	Abnormality of the endometrium
HP:0030127	Endometriosis
HP:0030129	Impaired ristocetin cofactor assay activity
HP:0030130	Impaired von Willibrand factor collagen binding activity
HP:0030131	Abnormal von Willebrand factor multimer distribution
HP:0030132	Absence of large von Willibrand factor multimers
HP:0030133	Abnormal presence of ultra-large von Willebrand factor multimers
HP:0030134	Total absence von Willebrand factor multimers
HP:0030135	Absence of intermediate von Willibrand factor multimers
HP:0030136	Enhanced ristocetin cofactor assay activity
HP:0030137	Prolonged bleeding following circumcision
HP:0030138	Excessive bleeding from superficial cuts
HP:0030139	Excessive bleeding after a venipuncture
HP:0030140	Oral cavity bleeding
HP:0030141	Abnormality of the posterior hairline
HP:0030142	Abnormal bowel sounds
HP:0030143	Hyperactive bowel sounds
HP:0030144	Hypoactive bowel sounds
HP:0030145	Lack of bowel sounds
HP:0030146	Abnormal liver parenchyma morphology
HP:0030147	Truncal titubation
HP:0030148	Heart murmur
HP:0030149	Cardiogenic shock
HP:0030150	Plasmacytosis
HP:0030151	Cholangitis
HP:0030152	obsolete Biliary tract neoplasm
HP:0030153	Cholangiocarcinoma
HP:0030154	Gallbladder perforation
HP:0030155	Scrotal pain
HP:0030156	Bence Jones Proteinuria
HP:0030157	Flank pain
HP:0030158	Cervical ectropion
HP:0030159	Cervical polyp
HP:0030160	Cervicitis
HP:0030161	Vaginal pruritus
HP:0030162	Glomerulomegaly
HP:0030163	Abnormal vascular physiology
HP:0030164	Jaw claudication
HP:0030165	Temporal artery tortuosity
HP:0030166	Night sweats
HP:0030167	Antimitochondrial antibody positivity
HP:0030168	Dilated superficial abdominal veins
HP:0030169	Gastric varix
HP:0030170	Cystic artery pseudoaneurysm
HP:0030171	Perirenal hematoma
HP:0030172	Peripheral amyelination
HP:0030173	Peripheral hypermyelination
HP:0030174	Increased peripheral myelin thickness
HP:0030175	Myelin tomacula
HP:0030176	Asymmetric peripheral demyelination
HP:0030177	Abnormality of peripheral nervous system electrophysiology
HP:0030178	Abnormality of central nervous system electrophysiology
HP:0030179	Abnormal peripheral action potential amplitude
HP:0030180	Oppenheim reflex
HP:0030181	Gordon reflex
HP:0030182	Tetraplegia/tetraparesis
HP:0030183	Impaired visually enhanced vestibulo-ocular reflex
HP:0030185	Isometric tremor
HP:0030186	Kinetic tremor
HP:0030187	Titubation
HP:0030188	Tremor by anatomical site
HP:0030190	Oral motor hypotonia
HP:0030191	Abnormal peripheral nervous system synaptic transmission
HP:0030192	Fatigable weakness of bulbar muscles
HP:0030193	Fatigable weakness of chewing muscles
HP:0030194	Fatigable weakness of speech muscles
HP:0030195	Fatigable weakness of swallowing muscles
HP:0030196	Fatigable weakness of respiratory muscles
HP:0030197	Fatigable weakness of skeletal muscles
HP:0030198	Fatigable weakness of distal limb muscles
HP:0030199	Fatigable weakness of neck muscles
HP:0030200	Fatiguable weakness of proximal limb muscles
HP:0030201	Response to drugs acting on neuromuscular transmission
HP:0030202	Favorable response of weakness to acetylcholine esterase inhibitors
HP:0030203	Unfavorable response of muscle weakness to acetylcholine esterase inhibitors
HP:0030205	Increased jitter at single fibre EMG
HP:0030206	EMG: incremental response of compound muscle action potential to repetitive nerve stimulation
HP:0030207	Paradoxical respiration
HP:0030208	Acetylcholine receptor antibody positivity
HP:0030209	Calcium channel antibody positivity
HP:0030210	Muscle specific kinase antibody positivity
HP:0030211	Slow pupillary light response
HP:0030212	Collectionism
HP:0030213	Emotional blunting
HP:0030214	Hypersexuality
HP:0030215	Inappropriate crying
HP:0030216	Inertia
HP:0030217	Limb apraxia
HP:0030218	Punding
HP:0030219	Semantic dementia
HP:0030220	Socially inappropriate behavior
HP:0030221	Sweet craving
HP:0030222	Visual agnosia
HP:0030223	Perseveration
HP:0030224	Abnormal muscle fiber desmin
HP:0030225	Accumulation of muscle fiber desmin
HP:0030226	Abnormal muscle fiber myotilin
HP:0030227	Accumulation of muscle fiber myotilin
HP:0030228	Abnormal muscle fiber valosin-containing protein
HP:0030229	Accumulation of muscle fiber valosin-containing protein
HP:0030230	Central core regions in muscle fibers
HP:0030231	Glycogen accumulation in muscle fiber lysosomes
HP:0030232	Increased sarcoplasmic glycogen
HP:0030233	Bethlem sign
HP:0030234	Highly elevated creatine phosphokinase
HP:0030235	Extremely elevated creatine phosphokinase
HP:0030236	Abnormality of muscle size
HP:0030237	Hand muscle weakness
HP:0030239	Hypoplasia of the upper arm musculature
HP:0030241	Hypoplasia of deltoid muscle
HP:0030242	Portal vein thrombosis
HP:0030243	Hepatic vein thrombosis
HP:0030244	Maternal fever in pregnancy
HP:0030245	Intrapartum fever
HP:0030246	Maternal first trimester fever
HP:0030247	Splanchnic vein thrombosis
HP:0030248	Mesenteric venous thrombosis
HP:0030249	Enanthema
HP:0030250	Pulmonary granulomatosis
HP:0030251	Absence of memory B cells
HP:0030252	Absence of mature B cells
HP:0030253	Defective T cell proliferation
HP:0030254	Nail bed hemorrhage
HP:0030255	Large intestinal polyposis
HP:0030256	Small intestinal polyposis
HP:0030257	Freckled genitalia
HP:0030258	Hyperpigmented genitalia
HP:0030259	Hypopigmented genitalia
HP:0030260	Microphallus
HP:0030261	Absent penis
HP:0030262	Narrow penis
HP:0030263	Torsion of the penis
HP:0030264	Webbed penis
HP:0030265	Wide penis
HP:0030266	Abnormality of the sacroiliac notch
HP:0030267	Calcification of the interosseus membrane of the forearm
HP:0030268	Hyperplastic callus formation
HP:0030269	Increased serum insulin-like growth factor 1
HP:0030270	Elevated red cell adenosine deaminase activity
HP:0030271	Reduced erythrocyte 2,3-diphosphoglycerate concentration
HP:0030272	Abnormal erythrocyte enzyme activity
HP:0030273	Reduced red cell adenosine deaminase activity
HP:0030274	Accessory scrotum
HP:0030275	Ectopic scrotum
HP:0030276	Small scrotum
HP:0030277	Abnormal vertebral pedicle morphology
HP:0030278	Hypoplastic vertebral pedicle
HP:0030279	Hypoplastic L5 vertebral pedicle
HP:0030280	Rib gap
HP:0030281	Cervical C3/C4 vertebral fusion
HP:0030282	Posterior rib gap
HP:0030283	Partial absence of the septum pellucidum
HP:0030284	Triangular tongue
HP:0030285	Splayed superior cerebellar peduncle
HP:0030286	Atrophic superior cerebellar peduncle
HP:0030289	Flattened femoral epiphysis
HP:0030290	Unossified sacrum
HP:0030291	Lower-limb metaphyseal irregularity
HP:0030292	Tibial metaphyseal irregularity
HP:0030293	Fibular metaphyseal irregularity
HP:0030294	Metaphyseal chondromatosis of tibia
HP:0030295	Metaphyseal chondromatosis of femur
HP:0030296	Metaphyseal chondromatosis of radius
HP:0030297	Metaphyseal chondromatosis of ulna
HP:0030298	Metaphyseal chondromatosis of humerus
HP:0030299	Distal femoral metaphyseal abnormality
HP:0030300	10 pairs of ribs
HP:0030301	Abnormality of the anterior commissure
HP:0030302	Agenesis of the anterior commissure
HP:0030303	Hypoplastic anterior commissure
HP:0030304	Abnormal number of vertebrae
HP:0030305	Decreased number of vertebrae
HP:0030306	11 thoracic vertebrae
HP:0030307	Flared lower limb metaphysis
HP:0030308	Flared distal tibial metaphysis
HP:0030309	Flared distal fibular metaphysis
HP:0030310	Upper extremity joint dislocation
HP:0030311	Lower extremity joint dislocation
HP:0030312	Obliteration of the calvarial diploe
HP:0030313	Abnormal periosteum morphology
HP:0030314	Periostosis
HP:0030318	Angular cheilitis
HP:0030319	Weakness of facial musculature
HP:0030320	Increased intervertebral space
HP:0030321	Abnormal vertebral artery morphology
HP:0030322	Vertebral artery hypoplasia
HP:0030323	Unilateral vertebral artery hypoplasia
HP:0030324	Bilateral vertebral artery hypoplasia
HP:0030325	Cervicomedullary schisis
HP:0030326	Abnormal macrophage count
HP:0030327	Abnormal osteoclast count
HP:0030328	Decreased osteoclast count
HP:0030329	Retinal thinning
HP:0030330	Multinucleated giant chondrocytes in epiphyseal cartilage
HP:0030331	Impaired stimulus-induced skin wrinkling
HP:0030332	obsolete Abnormal T cell morphology
HP:0030333	Abnormal alpha-beta T cell morphology
HP:0030334	Abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell morphology
HP:0030335	Abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell count
HP:0030336	Absence of CD4-positive, CD25-positive regulatory T cells
HP:0030337	Elevated CD4-positive, CD25-positive regulatory T cell count
HP:0030338	Abnormal circulating gonadotropin level
HP:0030339	Decreased circulating gonadotropin level
HP:0030340	obsolete Increased circulating gonadotropin level
HP:0030341	Decreased circulating follicle stimulating hormone level
HP:0030344	Decreased circulating luteinizing hormone level
HP:0030345	Abnormal circulating luteinizing hormone level
HP:0030346	Abnormal circulating follicle-stimulating hormone level
HP:0030347	Abnormal circulating androgen level
HP:0030348	Increased circulating androgen level
HP:0030349	Decreased circulating androgen level
HP:0030350	Erythematous papule
HP:0030351	Urticarial plaque
HP:0030352	Abnormal serum insulin-like growth factor 1 level
HP:0030353	Decreased serum insulin-like growth factor 1
HP:0030354	Abnormal serum interferon level
HP:0030355	Abnormal serum interferon-gamma level
HP:0030356	Increased serum interferon-gamma level
HP:0030357	Small cell lung carcinoma
HP:0030358	Non-small cell lung carcinoma
HP:0030359	Squamous cell lung carcinoma
HP:0030360	Large cell lung carcinoma
HP:0030361	Abnormality of eicosanoid metabolism
HP:0030362	Reduced muscle carnitine level
HP:0030363	Primary Caesarian section
HP:0030364	Secondary Caesarian section
HP:0030365	Vaginal birth after Caesarian
HP:0030366	Delivery by Odon device
HP:0030367	Finger hyperphalangy
HP:0030368	Hyperphalangy of the 2nd finger
HP:0030369	Induced vaginal delivery
HP:0030370	Abnormal proportion of naive B cells
HP:0030371	Increased proportion of naive B cells
HP:0030372	Decreased proportion of naive B cells
HP:0030373	Abnormal proportion of memory B cells
HP:0030374	Decreased proportion of memory B cells
HP:0030375	Increased proportion of memory B cells
HP:0030376	Abnormal proportion of immature B cells
HP:0030377	Increased proportion of immature B cells
HP:0030378	Decreased proportion of immature B cells
HP:0030379	Abnormal proportion of transitional B cells
HP:0030380	Decreased proportion of transitional B cells
HP:0030381	Increased proportion of transitional B cells
HP:0030383	Abnormal proportion of marginal zone B cells
HP:0030384	Decreased proportion of marginal zone B cells
HP:0030385	Increased proportion of marginal zone B cells
HP:0030386	Abnormal proportion of class-switched memory B cells
HP:0030387	Increased proportion of class-switched memory B cells
HP:0030388	Decreased proportion of class-switched memory B cells
HP:0030389	Abnormality of thromboxane metabolism
HP:0030390	Abnormality of leukotriene metabolism
HP:0030391	Spoken Word Recognition Deficit
HP:0030392	Choroid plexus carcinoma
HP:0030393	Endolymphatic sac tumor
HP:0030394	Fallopian tube carcinoma
HP:0030396	Abnormal platelet granule secretion
HP:0030397	Abnormal platelet dense granule secretion
HP:0030398	Abnormal platelet ATP dense granule secretion
HP:0030399	Abnormal platelet alpha granule secretion
HP:0030400	Abnormal platelet lysosome secretion
HP:0030401	Abnormal platelet dense granule ATP/ADP ratio
HP:0030402	Abnormal platelet aggregation
HP:0030403	Spontaneous platelet aggregation
HP:0030404	Glucagonoma
HP:0030405	Pancreatic endocrine tumor
HP:0030406	Primary peritoneal carcinoma
HP:0030407	Pineocytoma
HP:0030408	Pineoblastoma
HP:0030409	Renal transitional cell carcinoma
HP:0030410	Sebaceous gland carcinoma
HP:0030411	Jejunal adenocarcinoma
HP:0030412	Ileal adenocarcinoma
HP:0030413	Squamous cell carcinoma of the tongue
HP:0030414	Verrucous cell carcinoma of the tongue
HP:0030415	Sarcomatoid carcinoma of the tongue
HP:0030416	Vulvar neoplasm
HP:0030417	Squamous cell carcinoma of the vulva
HP:0030418	Vulvar melanoma
HP:0030419	Bartholin gland carcinoma
HP:0030420	Vulvar adenocarcinoma
HP:0030421	Epididymal neoplasm
HP:0030422	obsolete Papillary cystadenoma of the epididymis
HP:0030423	Splenic cyst
HP:0030424	Epididymal cyst
HP:0030425	Calcified ovarian cyst
HP:0030426	Ossifying fibroma
HP:0030427	Ossifying fibroma of the jaw
HP:0030428	Cutaneous myxoma
HP:0030429	Juvenile nasopharyngeal angiofibroma
HP:0030430	Neuroma
HP:0030431	Osteochondroma
HP:0030432	Chondroblastoma
HP:0030433	Osteoid osteoma
HP:0030434	Pilomatrixoma
HP:0030436	Fibrofolliculoma
HP:0030437	Anal canal neoplasm
HP:0030438	Anal canal squamous cell carcinoma
HP:0030439	Anal canal adenocarcinoma
HP:0030440	Anal margin neoplasm
HP:0030441	Anal margin Paget's disease
HP:0030442	Anal margin squamous cell carcinoma
HP:0030443	Anal margin basal cell carcinoma
HP:0030444	Anal margin melanoma
HP:0030445	Pulmonary carcinoid tumor
HP:0030446	Atypical pulmonary carcinoid tumor
HP:0030447	Merkel cell skin cancer
HP:0030448	Soft tissue sarcoma
HP:0030449	Therapeutic abortion
HP:0030450	Neuroplasm of the autonomic nervous system
HP:0030451	Mesenteric cyst
HP:0030452	Chylolymphatic mesenteric cyst
HP:0030453	Abnormal visual electrophysiology
HP:0030454	Abnormal electrooculogram
HP:0030455	Abnormality of pattern visual evoked potentials
HP:0030456	Abnormality of pattern onset/offset visual evoked potentials
HP:0030457	Abnormal amplitude of pattern onset/offset visual evoked potentials
HP:0030458	Abnormal timing of pattern onset/offset visual evoked potentials
HP:0030460	Abnormal timing of pattern reversal visual evoked potentials
HP:0030461	Abnormal timing of flash visual evoked potentials
HP:0030462	Abnormal amplitude of flash visual evoked potentials
HP:0030463	Asymmetrical distribution of flash visual evoked potentials
HP:0030464	Asymmetrical distribution of pattern reversal visual evoked potentials
HP:0030465	Undetectable light-adapted electroretinogram
HP:0030466	Abnormal full-field electroretinogram
HP:0030467	Abnormal pattern electroretinogram
HP:0030468	Abnormal multifocal electroretinogram
HP:0030469	Abnormal dark-adapted electroretinogram
HP:0030470	Abnormal dark-adapted bright flash electroretinogram
HP:0030471	Abnormal dark-adapted dim flash electroretinogram
HP:0030472	Abnormal light-adapted single flash electroretinogram
HP:0030473	Abnormal light-adapted flicker electroretinogram
HP:0030474	Undetectable dark-adapted electroretinogram
HP:0030475	Abnormal timing of dark-adapted dim flash electroretinogram
HP:0030476	Abnormal amplitude of dark-adapted dim flash electroretinogram
HP:0030477	Abnormal timing of dark-adapted bright flash electroretinogram
HP:0030478	Abnormal amplitude of dark-adapted bright flash electroretinogram
HP:0030479	Abnormal amplitude of light-adapted flicker electroretinogram
HP:0030480	Abnormal timing of light-adapted flicker electroretinogram
HP:0030481	Abnormal amplitude of light-adapted single flash electroretinogram
HP:0030482	Abnormal timing of light-adapted single flash electroretinogram
HP:0030483	Reduced amplitude of dark-adapted bright flash electroretinogram a-wave
HP:0030484	Supernormal dark-adapted bright flash electroretinogram b-wave
HP:0030485	Abnormal amplitude of pattern electroretinogram
HP:0030486	Abnormal timing of pattern electroretinogram
HP:0030487	Abnormal P50/N95 ratio of pattern electroretinogram
HP:0030488	Abnormal central response of multifocal electroretinogram
HP:0030489	Abnormal paracentral response of multifocal electroretinogram
HP:0030490	Exudative vitreoretinopathy
HP:0030491	Choriocapillaris atrophy
HP:0030493	Abnormality of foveal pigmentation
HP:0030494	Macular microaneurysm/hemorrhage
HP:0030495	Abnormality of macular vasculature
HP:0030496	Macular exudate
HP:0030497	Macular cotton wool spot
HP:0030498	Macular thickening
HP:0030499	Macular drusen
HP:0030500	Yellow/white lesions of the macula
HP:0030501	Macular crystals
HP:0030502	Retinoschisis
HP:0030503	Macular telangiectasia
HP:0030504	Grouped congenital hypertrophy of retinal pigment epithelium
HP:0030505	Nummular pigmentation of the fundus
HP:0030506	Yellow/white lesions of the retina
HP:0030507	Retinal crystals
HP:0030508	Retinal cavernous hemangioma
HP:0030509	Retinal racemose hemangioma
HP:0030510	Combined hamartoma of the retinal pigment epithelium and retina
HP:0030511	Bradyopsia
HP:0030512	Difficulty adjusting to changes in luminance
HP:0030513	Difficulty adjusting from light to dark
HP:0030514	Difficulty adjusting from dark to light
HP:0030515	Moderately reduced visual acuity
HP:0030516	Homonymous hemianopia
HP:0030517	Heteronymous hemianopia
HP:0030518	Congruous homonymous hemianopia
HP:0030519	Congruous heteronymous hemianopia
HP:0030520	Binasal hemianopia
HP:0030521	Bitemporal hemianopia
HP:0030522	Mild constriction of peripheral visual field
HP:0030523	obsolete Peripheral visual field constriction with 40-50 degrees central field preserved
HP:0030524	obsolete Peripheral visual field constriction with 30-39 degrees central field preserved
HP:0030525	Moderate constriction of peripheral visual field
HP:0030526	Severe constriction of peripheral visual field
HP:0030527	Very severe constriction of peripheral visual field
HP:0030528	Paracentral scotoma
HP:0030529	Ring scotoma
HP:0030530	Arcuate scotoma
HP:0030531	Altitudinal visual field defect
HP:0030532	Visual acuity test abnormality
HP:0030533	Abnormal unaided visual acuity test
HP:0030534	Abnormal best corrected visual acuity test
HP:0030535	Abnormal pinhole visual acuity test
HP:0030536	Unaided visual acuity 0.1 LogMAR
HP:0030537	Unaided visual acuity 0.2 LogMAR
HP:0030538	Unaided visual acuity 0.3 LogMAR
HP:0030539	Unaided visual acuity 0.4 LogMAR
HP:0030540	Unaided visual acuity 0.5 LogMAR
HP:0030541	Unaided visual acuity 0.6 LogMAR
HP:0030542	Unaided visual acuity 0.7 LogMAR
HP:0030543	Unaided visual acuity 0.8 LogMAR
HP:0030544	Unaided visual acuity 0.9 LogMAR
HP:0030545	Unaided visual acuity 1.0 LogMAR
HP:0030546	Unaided visual acuity 1.1 LogMAR
HP:0030547	Unaided visual acuity 1.2 LogMAR
HP:0030548	Unaided visual acuity 1.3 LogMAR
HP:0030549	Unaided visual acuity 2.0 LogMAR
HP:0030550	Unaided visual acuity 3.0 LogMAR
HP:0030551	Visual acuity light perception with projection
HP:0030552	Visual acuity light perception without projection
HP:0030553	Visual acuity no light perception
HP:0030554	Best corrected visual acuity 0.1 LogMAR
HP:0030555	Best corrected visual acuity 0.2 LogMAR
HP:0030556	Best corrected visual acuity 0.3 LogMAR
HP:0030557	Best corrected visual acuity 0.4 LogMAR
HP:0030558	Best corrected visual acuity 0.5 LogMAR
HP:0030559	Best corrected visual acuity 0.7 LogMAR
HP:0030560	Best corrected visual acuity 0.6 LogMAR
HP:0030561	Best corrected visual acuity 0.8 LogMAR
HP:0030562	Best corrected visual acuity 0.9 LogMAR
HP:0030563	Best corrected visual acuity 1.0 LogMAR
HP:0030564	Best corrected visual acuity 1.1 LogMAR
HP:0030565	Best corrected visual acuity 1.2 LogMAR
HP:0030566	Best corrected visual acuity 1.3 LogMAR
HP:0030567	Best corrected visual acuity 2.0 LogMAR
HP:0030568	Best corrected visual acuity 3.0 LogMAR
HP:0030569	Pinhole visual acuity 0.1 LogMAR
HP:0030570	Pinhole visual acuity 0.2 LogMAR
HP:0030571	Pinhole visual acuity 0.3 LogMAR
HP:0030572	Pinhole visual acuity 0.4 LogMAR
HP:0030573	Pinhole visual acuity 0.5 LogMAR
HP:0030574	Pinhole visual acuity 0.6 LogMAR
HP:0030575	Pinhole visual acuity 0.7 LogMAR
HP:0030576	Pinhole visual acuity 0.8 LogMAR
HP:0030577	Pinhole visual acuity 0.9 LogMAR
HP:0030578	Pinhole visual acuity 1.0 LogMAR
HP:0030579	Pinhole visual acuity 1.1 LogMAR
HP:0030580	Pinhole visual acuity 1.2 LogMAR
HP:0030581	Pinhole visual acuity 1.3 LogMAR
HP:0030582	Pinhole visual acuity 2.0 LogMAR
HP:0030583	Pinhole visual acuity 3.0 LogMAR
HP:0030584	Color vision test abnormality
HP:0030585	Red desaturation
HP:0030586	Abnormal Ishihara plate test
HP:0030587	Abnormal Hardy-Rand-Rittler plate test
HP:0030588	Abnormal visual field test
HP:0030589	Abnormal confrontational visual field test
HP:0030590	Abnormal Amsler grid test
HP:0030591	Abnormal kinetic perimetry test
HP:0030592	Abnormal static perimetry test
HP:0030593	Abnormal manual kinetic perimetry test
HP:0030594	Abnormal automated kinetic perimetry test
HP:0030595	Abnormal static automated perimetry test
HP:0030596	Abnormal Humphrey SITA 30-2 perimetry test
HP:0030597	Abnormal Humphrey SITA 24-2 perimetry test
HP:0030598	Abnormal Humphrey SITA 10-2 perimetry test
HP:0030599	Abnormal Estermann grid perimetry test
HP:0030601	Abnormal posterior segment imaging
HP:0030602	Abnormal fundus autofluorescence imaging
HP:0030603	Abnormal optical coherence tomography
HP:0030604	Abnormal fundus fluorescein angiography
HP:0030605	Abnormal indocyanine green angiography
HP:0030606	Abnormal OCT-measured macular thickness
HP:0030607	Reduced OCT-measured macular thickness
HP:0030608	Increased OCT-measured macular thickness
HP:0030609	Photoreceptor layer loss on macular OCT
HP:0030610	Photoreceptor outer segment loss on macular OCT
HP:0030611	Retinal pigment epithelial loss on macular OCT
HP:0030612	Abnormal retinal morphology on macular OCT
HP:0030613	Abnormal foveal morphology on macular OCT
HP:0030614	Foveal photoreceptor layer loss on macular OCT
HP:0030615	Foveal photoreceptor outer segment loss on macular OCT
HP:0030616	Foveal retinal pigment epithelial loss on macular OCT
HP:0030617	Abnormal OCT-measured foveal thickness
HP:0030618	Increased OCT-measured foveal thickness
HP:0030619	Reduced OCT-measured foveal thickness
HP:0030620	Inner retinal layer loss on macular OCT
HP:0030621	Foveal inner retinal layer loss on macular OCT
HP:0030622	Abnormal foveal pit on macular OCT
HP:0030623	Intraretinal hyporeflective spaces on macular OCT
HP:0030624	Subretinal hyporeflective spaces on macular OCT
HP:0030625	Hyporeflective spaces on macular OCT
HP:0030626	Foveal intraretinal hyporeflective spaces on macular OCT
HP:0030627	Foveal hyporeflective spaces on macular OCT
HP:0030628	Foveal subretinal hyporeflective spaces on macular OCT
HP:0030629	Perifoveal ring of hyperautofluorescence
HP:0030630	Irregular central macular autofluorescence
HP:0030631	Hyperautofluorescent macular lesion
HP:0030632	Hypoautofluorescent macular lesion
HP:0030633	Perifoveal ring of hyperautofluorescence surrounded by normal autofluorescence
HP:0030634	Perifoveal ring of hyperautofluorescence surrounded by abnormal autofluorescence
HP:0030635	Retinal dystrophy with early macular involvement
HP:0030636	Occult macular dystrophy
HP:0030637	Congenital stationary cone dysfunction
HP:0030638	Congenital stationary night blindness with normal fundus
HP:0030639	Congenital stationary night blindness with abnormal fundus
HP:0030640	Complete congenital stationary night blindness
HP:0030641	Incomplete congenital stationary night blindness
HP:0030642	Fundus albipunctatus
HP:0030643	Vitelliform-like retinal lesions
HP:0030644	Blind-spot enlargment
HP:0030645	Central
HP:0030646	Peripheral
HP:0030647	Paracentral
HP:0030648	Midperipheral
HP:0030649	Pericentral
HP:0030650	Focal
HP:0030651	Multifocal
HP:0030652	Vitreous haze
HP:0030654	Umbilical cord cyst
HP:0030655	Umbilical cord knot
HP:0030656	Umbilical vein varix
HP:0030657	Umbilical cord hematoma
HP:0030658	Marginal umbilical cord insertion
HP:0030659	Velamentous cord insertion
HP:0030660	Furcate cord insertion
HP:0030661	Vitreous snowballs
HP:0030662	Vitreous inflammatory cells
HP:0030663	Optically empty vitreous
HP:0030664	Beevor's sign
HP:0030665	Rubral tremor
HP:0030666	Retinal neovascularization
HP:0030667	Peripheral retinal neovascularization
HP:0030668	Periorbital dermoid cyst
HP:0030669	Abnormal ocular adnexa morphology
HP:0030670	Hamartoma of the orbital region
HP:0030671	Abnormal common tendinous ring morphology
HP:0030672	Asteroid hyalosis
HP:0030673	Erosive vitreoretinopathy
HP:0030674	Antenatal onset
HP:0030675	Contracture of proximal interphalangeal joints of 2nd-5th fingers
HP:0030676	Satyr ear
HP:0030677	Mozart ear
HP:0030679	Ash-leaf spot
HP:0030680	Abnormality of cardiovascular system morphology
HP:0030681	Abnormal morphology of myocardial trabeculae
HP:0030682	Left ventricular noncompaction
HP:0030683	Vaginitis
HP:0030684	Abnormal adiponectin level
HP:0030685	Decreased adiponectin level
HP:0030686	Increased adiponectin level
HP:0030687	Abnormal glucagon level
HP:0030688	Increased glucagon level
HP:0030689	Decreased glucagon level
HP:0030690	Gingival cleft
HP:0030691	Divergence nystagmus
HP:0030692	Brain neoplasm
HP:0030693	Supratentorial neoplasm
HP:0030694	Pineal parenchymal cell neoplasm
HP:0030706	Ranula
HP:0030707	Unilateral lung agenesis
HP:0030708	Myeloschisis
HP:0030709	Myelocystocele
HP:0030710	Lipomeningocele
HP:0030711	Hydrocolpos
HP:0030712	Uterine synechiae
HP:0030713	Vein of Galen aneurysmal malformation
HP:0030714	Subchorionic thrombohematoma
HP:0030715	Bronchial atresia
HP:0030716	Acrania
HP:0030717	Meconium peritonitis
HP:0030718	Right atrial enlargement
HP:0030719	Unguarded tricuspid valve
HP:0030720	Subchorionic septal cyst
HP:0030721	Tetraphocomelia
HP:0030722	Ectopic liver
HP:0030723	Congenital megalourethra
HP:0030724	Central nervous system cyst
HP:0030725	Neurenteric cyst
HP:0030726	Spinal neurenteric cyst
HP:0030727	Intracranial neurenteric cyst
HP:0030728	Meromelia
HP:0030729	Frontoethmoidal meningocele
HP:0030730	Parietal meningocele
HP:0030731	Carcinoma
HP:0030732	Dysplastic tricuspid valve
HP:0030733	Vesicoallantoic abdominal wall defect
HP:0030735	Ureterovesical junction obstruction
HP:0030736	Sacrococcygeal teratoma
HP:0030737	Altman type I sacrococcygeal teratoma
HP:0030738	Altman type II sacrococcygeal teratoma
HP:0030739	Altman type III sacrococcygeal teratoma
HP:0030740	Anomalous muscle bundle of the right ventricle
HP:0030741	Mediastinal teratoma
HP:0030742	Glial remnants posterior to lens
HP:0030743	Glial remnants anterior to the optic disc
HP:0030744	Hyaloid vascular remnant and retrolental mass
HP:0030745	Dilatation of the ductus arteriosus
HP:0030746	Intraventricular hemorrhage
HP:0030747	Preterm intraventricular hemorrhage
HP:0030748	Grade I preterm intraventricular hemorrhage
HP:0030749	Grade II preterm intraventricular hemorrhage
HP:0030750	Grade III preterm intraventricular hemorrhage
HP:0030751	Grade IV preterm intraventricular hemorrhage
HP:0030752	Dacryocystocele
HP:0030753	Intrauterine fetal demise of one twin after midgestation
HP:0030754	Allantoic cyst
HP:0030755	Craniofacial teratoma
HP:0030756	Erythrodontia
HP:0030757	Tooth abscess
HP:0030758	Periapical tooth abscess
HP:0030759	Adipocyte hypertrophy
HP:0030760	Renal fibrosis
HP:0030761	obsolete Renal glomerular fibrosis
HP:0030762	Mesangiolysis
HP:0030763	Amniotic Sheet
HP:0030764	Ochronosis
HP:0030765	Sleep terror
HP:0030766	Ear pain
HP:0030767	Epignathus
HP:0030769	Exencephaly
HP:0030770	Craniorachischisis
HP:0030771	Mallet finger
HP:0030772	Proximal femoral focal deficiency
HP:0030773	Internuclear ophthalmoplegia
HP:0030774	Mitochondrial swelling
HP:0030775	Modic type vertebral endplate changes
HP:0030776	Modic type I vertebral endplate changes
HP:0030777	Modic type II vertebral endplate changes
HP:0030778	Modic type III vertebral endplate changes
HP:0030779	Ethmocephaly
HP:0030780	Abnormality of the protein C anticoagulant pathway
HP:0030781	Increased circulating free fatty acid level
HP:0030782	Abnormal serum interleukin level
HP:0030783	Increased serum interleukin-6
HP:0030784	Anomia
HP:0030785	Mediastinal cystic lymphangioma
HP:0030786	Photopsia
HP:0030787	Cerumen abnormality
HP:0030788	Impacted cerumen
HP:0030789	Excessive cerumen
HP:0030790	Abnormal cerumen color
HP:0030791	Abnormal jaw morphology
HP:0030792	Jaw neoplasm
HP:0030793	Jaw swelling
HP:0030794	Abnormal C-peptide level
HP:0030795	Reduced C-peptide level
HP:0030796	Increased C-peptide level
HP:0030797	Reduced volume of central subdivision of bed nucleus of stria terminalis
HP:0030798	Abnormality of the bed nucleus of stria terminalis
HP:0030799	Scaphocephaly
HP:0030800	Abnormal visual accommodation
HP:0030801	Reduced visual accommodation
HP:0030802	Lower eyelid retraction
HP:0030803	Platonychia
HP:0030804	Trachyonychia
HP:0030805	Absent lunula
HP:0030806	Fast-growing nails
HP:0030807	Abnormal nail growth
HP:0030808	Ragged cuticle
HP:0030809	Abnormal tongue morphology
HP:0030810	Abnormal tongue physiology
HP:0030811	Tongue pain
HP:0030812	Enlarged tonsils
HP:0030813	Absent tonsils
HP:0030814	Orange discoloured tonsils
HP:0030815	Lipoma of the tongue
HP:0030816	Gingival recession
HP:0030817	Beaked nails
HP:0030818	Central nail canal
HP:0030819	Ski jump nail
HP:0030820	Hooded eyelid
HP:0030821	Hooded lower eyelid
HP:0030822	Hooded upper eyelid
HP:0030823	Scleral thickening
HP:0030824	Mizuo phenomenon
HP:0030825	Absent foveal reflex
HP:0030826	Eyelid fasciculation
HP:0030828	Wheezing
HP:0030829	Abnormal breath sound
HP:0030830	Crackles
HP:0030831	Rhonchi
HP:0030832	Vitreous strands
HP:0030833	Neck pain
HP:0030834	Shoulder pain
HP:0030835	Elbow pain
HP:0030836	Wrist pain
HP:0030837	Finger pain
HP:0030838	Hip pain
HP:0030839	Knee pain
HP:0030840	Ankle pain
HP:0030841	Toe pain
HP:0030842	Choking episodes
HP:0030843	Cardiac amyloidosis
HP:0030844	Undetectable pattern electroretinogram
HP:0030845	Heliotrope rash of eyelid
HP:0030846	Abnormality of venous physiology
HP:0030847	Abnormal jugular venous pressure
HP:0030848	Elevated jugular venous pressure
HP:0030849	Hepatojugular reflux
HP:0030850	Abnormal pulse pressure
HP:0030851	Low pulse pressure
HP:0030852	High pulse pressure
HP:0030853	Heterotaxy
HP:0030854	Scleral staphyloma
HP:0030855	Anterior staphyloma
HP:0030856	Posterior staphyloma
HP:0030857	Eye movement-induced pain
HP:0030858	Addictive behavior
HP:0030859	Topoisomerase I antibody positivity
HP:0030860	Abnormal CSF amyloid level
HP:0030861	Decreased CSF amyloid level
HP:0030862	Elevated CSF amyloid level
HP:0030863	Nasal flaring
HP:0030864	Intercostal retractions
HP:0030865	Large elbow
HP:0030866	Large knee
HP:0030867	Vertical orbital dystopia
HP:0030868	Monorchism
HP:0030869	Anorchism
HP:0030870	Abnormality of spinal facet joint
HP:0030871	Facet joint arthrosis
HP:0030872	Abnormal cardiac ventricular function
HP:0030873	Anticentromere antibody positivity
HP:0030874	Oxygen desaturation on exertion
HP:0030875	Abnormality of pulmonary circulation
HP:0030876	Increased pulmonary capillary wedge pressure
HP:0030877	Obstructive deficit on pulmonary function testing
HP:0030878	Abnormality on pulmonary function testing
HP:0030879	Interlobular septal thickening on pulmonary HRCT
HP:0030880	Raynaud phenomenon
HP:0030881	Shoulder impingement
HP:0030882	Coronary artery aneurysm
HP:0030883	Femoroacetabular Impingement
HP:0030884	Gastrojejunal tube feeding in infancy
HP:0030885	Recurrent parasitic infections
HP:0030886	Abnormal lymphocyte apoptosis
HP:0030887	Increased lymphocyte apoptosis
HP:0030888	C3 nephritic factor positivity
HP:0030889	Congenital shortened small intestine
HP:0030890	Hyperintensity of cerebral white matter on MRI
HP:0030891	Periventricular white matter hyperdensities
HP:0030892	Deep cerebral white matter hyperdensities
HP:0030893	Abnormal response to short acting pulmonary vasodilator
HP:0030894	Insufficient response to short acting pulmonary vasodilator
HP:0030895	Abnormal gastrointestinal motility
HP:0030896	Abnormal gastrointestinal transit time
HP:0030897	Decreased intestinal transit time
HP:0030898	Pruritis on abdomen
HP:0030899	Pruritis on hand
HP:0030900	Pruritus on foot
HP:0030901	Pruritis on breast
HP:0030902	Palmomental reflex
HP:0030903	Grasp reflex
HP:0030904	Glabellar reflex
HP:0030905	Snout reflex
HP:0030906	Suck reflex
HP:0030907	Thunderclap headache
HP:0030908	Liver kidney microsome type 1 antibody positivity
HP:0030909	Anti-liver cytosolic antigen type 1 antibody positivity
HP:0030911	Bifid clitoris
HP:0030912	Duplicated clitoris
HP:0030913	Exaggerated rugosity of the labia majora
HP:0030914	Abnormal peristalsis
HP:0030915	Cerebellar edema
HP:0030917	Low APGAR score
HP:0030918	Low 1-minute APGAR score
HP:0030919	Low 5-minute APGAR score
HP:0030920	5-minute APGAR score of 0
HP:0030921	5-minute APGAR score of 1
HP:0030922	5-minute APGAR score of 2
HP:0030923	5-minute APGAR score of 3
HP:0030924	5-minute APGAR score of 4
HP:0030925	5-minute APGAR score of 5
HP:0030926	5-minute APGAR score of 6
HP:0030927	1-minute APGAR score of 0
HP:0030928	1-minute APGAR score of 1
HP:0030929	1-minute APGAR score of 2
HP:0030930	1-minute APGAR score of 3
HP:0030931	1-minute APGAR score of 4
HP:0030932	1-minute APGAR score of 5
HP:0030933	1-minute APGAR score of 6
HP:0030934	Oral erythroplakia
HP:0030935	Abnormality of intestinal smooth muscle morphology
HP:0030936	Abnormal layering of muscularis propria
HP:0030937	Fibrotic muscularis propria
HP:0030938	Enteric intraneuronal nuclear inclusion bodies
HP:0030939	Palpebral thickening
HP:0030943	Vulvodynia
HP:0030946	Conjunctival papillae
HP:0030947	Conjunctival follicles
HP:0030948	Elevated gamma-glutamyltransferase activity
HP:0030949	Glomerular deposits
HP:0030950	Pulmonary venous hypertension
HP:0030951	Skeletal muscle fibrosis
HP:0030952	Birdshot choroidal lesions
HP:0030953	Conjunctival hyperemia
HP:0030955	Alcoholism
HP:0030956	Abnormality of cardiovascular system electrophysiology
HP:0030957	Ventricular septal aneurysm
HP:0030958	Membranous ventricular septal aneurysm
HP:0030959	Muscular ventricular septal aneurysm
HP:0030960	obsolete Abnormal pupillary morphology
HP:0030961	Microspherophakia
HP:0030962	Abnormal morphology of the great vessels
HP:0030963	obsolete Abnormal aortic morphology
HP:0030964	Abnormal aortic physiology
HP:0030965	Aortic stiffness
HP:0030966	Abnormal pulmonary artery morphology
HP:0030967	Abnormal pulmonary artery physiology
HP:0030968	Abnormal pulmonary vein morphology
HP:0030969	Abnormal pulmonary vein physiology
HP:0030970	Abnormal vena cava physiology
HP:0030971	obsolete Abnormal vena cava morphology
HP:0030972	Abnormal systemic blood pressure
HP:0030973	Postexertional malaise
HP:0030974	Cryptozoospermia
HP:0030975	Pontine tegmental cap
HP:0030976	Abnormal factor VIII activity
HP:0030977	Increased factor VIII activity
HP:0030978	Decreased CSF/serum albumin ratio
HP:0030979	Dilatation of large choroidal vessels
HP:0030980	Reduced brain glutamine level by MRS
HP:0030981	Abnormal CSF/serum albumin ratio
HP:0030983	Ovarian thecoma
HP:0030984	Abnormal serum bile acid concentration
HP:0030985	Decreased serum bile concentration
HP:0030986	Biliary epithelial hyperplasia
HP:0030987	Suppurative cholangitis
HP:0030988	Granulomatous cholangitis
HP:0030989	Lymphoid cholangitis
HP:0030990	Pleomorphic cholangitis
HP:0030991	Sclerosing cholangitis
HP:0030992	Abnormal pancreatic duct morphology
HP:0030993	Duplication of pancreatic duct
HP:0030994	Pancreas divisum
HP:0030995	Peritoneal effusion
HP:0030996	Megaduodenum
HP:0030997	Atretic vas deferens
HP:0030998	Cerebrospinal fluid rhinorrhoea
HP:0030999	Abnormal vestibular saccule morphology
HP:0031000	Vestibular saccular degeneration
HP:0031001	Minifascicle formation
HP:0031002	Neuritis
HP:0031003	Polyneuritis
HP:0031004	Hemiareflexia
HP:0031005	Hyperalgesia
HP:0031006	Acroparesthesia
HP:0031007	Orofacial action-specific dystonia induced by speech
HP:0031008	Lingual dystonia
HP:0031009	Ainhum
HP:0031010	Hyperphalangy of the 3rd finger
HP:0031011	Fatty streak
HP:0031012	Thin-cap fibroatheroma
HP:0031013	Ankylosis
HP:0031014	Arteria lusoria
HP:0031015	Intrahepatic portal vein sclerosis
HP:0031016	Alternating radiolucent and radiodense metaphyseal lines
HP:0031017	Swiss cheese atrial septal defect
HP:0031018	Eccrine syringofibroadenoma
HP:0031019	Pyknotic bone marrow neutrophils
HP:0031020	Bone marrow hypercellularity
HP:0031021	Squamous Papilloma
HP:0031022	Oropharyngeal squamous papilloma
HP:0031023	Multiple mucosal neuromas
HP:0031024	Cylindroma
HP:0031025	Gastric leiomyosarcoma
HP:0031026	Snail-like ilia
HP:0031027	Internal notch of the femoral head
HP:0031028	Lactescent serum
HP:0031029	Elevated carcinoembryonic antigen level
HP:0031030	Elevated carcinoma antigen 125 level
HP:0031031	Abnormal retinol-binding protein level
HP:0031032	Decreased retinol-binding protein level
HP:0031033	Impaired urinary acidification
HP:0031034	Abnormal insulin like growth factor binding protein acid labile subunit level
HP:0031035	Chronic infection
HP:0031036	Reduced growth-hormone binding protein level
HP:0031037	Reduced insulin-like factor 3 level
HP:0031038	Spermatogenesis maturation arrest
HP:0031039	Early spermatogenesis maturation arrest
HP:0031040	Late spermatogenesis maturation arrest
HP:0031041	Obstruction of the superior vena cava
HP:0031042	Strawberry tongue
HP:0031043	Type A4 brachydactyly
HP:0031044	Type A5 brachydactyly
HP:0031045	Acral blistering
HP:0031046	Absent soft palate
HP:0031047	Paraproteinemia
HP:0031048	Light-chain paraproteinemia
HP:0031049	Heavy-chain paraproteinemia
HP:0031050	Whole-immunoglobulin paraproteinemia
HP:0031051	Tarsal sclerosis
HP:0031052	Elevated vascular endothelial growth factor level
HP:0031053	Coarctation in the transverse aortic arch
HP:0031054	Long segment coarctation of the aorta
HP:0031055	Abnormal branching pattern of left aortic arch
HP:0031056	Fusiform cerebral aneurysm
HP:0031057	Skin fissure
HP:0031058	Impairment of activities of daily living
HP:0031059	Impaired ability to bathe oneself
HP:0031060	Impaired ability to dress oneself
HP:0031061	Impaired toileting ability
HP:0031062	Impaired transferring ability
HP:0031063	Impaired feeding ability
HP:0031064	Impaired continence
HP:0031065	Abnormal ovarian morphology
HP:0031066	Abnormal ovarian physiology
HP:0031067	Empty ovarian follicle
HP:0031068	Increased femoral torsion
HP:0031069	Abnormal femoral torsion
HP:0031070	Decreased femoral torsion
HP:0031071	Abnormal endocrine morphology
HP:0031072	Abnormal endocrine physiology
HP:0031073	Abnormal response to endocrine stimulation test
HP:0031074	Abnormal response to ACTH stimulation test
HP:0031075	Abnormal response to insulin tolerance test
HP:0031076	Impaired cortisol response to insulin stimulation test
HP:0031077	Abnormal response to corticotropin releasing hormone stimulation test
HP:0031078	Impaired cortisol response to corticotropin releasing hormone stimulation test
HP:0031079	Impaired growth-hormone response to insulin stimulation test
HP:0031080	Abnormal response to glucagon stimulation test
HP:0031081	Impaired cortisol response to glucagon stimulation test
HP:0031082	Impaired growth-hormone response to glucagon stimulation test
HP:0031083	Abnormal response to human chorionic gonadotrophin stimulation test
HP:0031084	Excessive insulin response to glucagon test
HP:0031085	Decreased prealbumin level
HP:0031086	Ectopic ovary
HP:0031087	Absent pubertal growth spurt
HP:0031088	Vaginal dryness
HP:0031089	Palatal edema
HP:0031090	Finger dactylitis
HP:0031091	Toe dactylitis
HP:0031092	Spindle-shaped finger
HP:0031093	Abnormal breast morphology
HP:0031094	Abnormal breast physiology
HP:0031095	Abnormal humerus morphology
HP:0031096	Delayed vertebral ossification
HP:0031097	Abnormal thyroid-stimulating hormone level
HP:0031098	Decreased thyroid-stimulating hormone level
HP:0031099	Abnormal circulating inhibin level
HP:0031100	Decreased inhibin B level
HP:0031101	Abnormal antimullerian hormone level
HP:0031102	Increased antimullerian hormone level
HP:0031103	Decreased antimullerian hormone level
HP:0031104	Insulin receptor antibody positivity
HP:0031105	Abnormal uterus morphology
HP:0031106	T-shaped uterus
HP:0031107	Decreased fibular diameter
HP:0031108	Triceps weakness
HP:0031109	Agalactia
HP:0031110	Twin-to-twin transfusion
HP:0031111	Cutaneous hamartoma
HP:0031117	Purely bicuspid aortic valve
HP:0031118	Single raphe bicuspid aortic valve
HP:0031119	Bicuspid aortic valve with right-left cusp fusion
HP:0031120	Bicuspid aortic valve with right-noncoronary cusp fusion
HP:0031121	Bicuspid aortic valve with left-noncoronary cusp fusion
HP:0031122	Two-raphe bicuspid aortic valve
HP:0031123	Recurrent gastroenteritis
HP:0031124	Decreased platelet thromboxane A2 receptor
HP:0031125	Decreased platelet alpha-2A-adrenergic receptor
HP:0031126	Impaired clot retraction
HP:0031127	Impaired convulxin-induced platelet aggregation
HP:0031128	Impaired collagen-related peptide-induced platelet aggregation
HP:0031129	Impaired phorbol myristate acetate-induced platelet aggregation
HP:0031130	Impaired calcium ionophore-induced platelet aggregation
HP:0031131	Abnormal plalelet phosphatidylserine exposure
HP:0031132	Impaired annexin V binding to platelet phosphatidylserine
HP:0031133	Increased annexin V binding to platelet phosphatidylserine
HP:0031134	Cor triatrium sinister
HP:0031135	Triggered by physical trauma
HP:0031136	Decreased acrosin in sperm head
HP:0031137	Storage in hepatocytes
HP:0031138	Abnormal B-type natriuretic peptide level
HP:0031139	Frog-leg posture
HP:0031140	Abnormal liver sonography
HP:0031141	Increased hepatic echogenicity
HP:0031142	Abnormal hepatic echogenicity
HP:0031143	Decreased hepatic echogenicity
HP:0031144	Coarsened hepatic echotexture
HP:0031145	Starry sky appearance on hepatic sonography
HP:0031146	Impaired oral bolus formation
HP:0031150	Vitreomacular adhesion
HP:0031151	Vitreomacular traction
HP:0031152	Full-thickness macular hole
HP:0031153	Membranous vitreous appearance
HP:0031154	Beaded vitreous appearance
HP:0031155	Increased Arden ratio of electrooculogram
HP:0031156	Decreased platelet glycoprotein Ib
HP:0031157	Carotid cavernous fistula
HP:0031158	Widened atrophic scar
HP:0031159	Thinning of Descemet membrane
HP:0031160	Myelokathexis
HP:0031161	Reduced brain glutamate level by MRS
HP:0031162	Impaired oropharyngeal swallow response
HP:0031163	Low femoral bone density
HP:0031164	Growth arrest lines
HP:0031165	Multifocal seizures
HP:0031166	Eyelid myokymia
HP:0031167	Triggered by ingestion of potassium-rich food
HP:0031169	Postterm pregnancy
HP:0031170	Female fetal virilization
HP:0031171	Femoral spur
HP:0031172	Sectoral retinitis pigmentosa
HP:0031173	Tibial spur
HP:0031174	Double-layered patella
HP:0031175	Absent cervical vertebra
HP:0031176	Absent thoracic vertebra
HP:0031177	Finger flexor weakness
HP:0031178	Fixed head retroflexion
HP:0031179	Nuchal rigidity
HP:0031180	Erythema migrans
HP:0031181	Necrolytic migratory erythema
HP:0031185	Increased NT-proBNP level
HP:0031186	Abnormal circulating deoxycorticosterone level
HP:0031187	Abnormality of circulating pregnenolone level
HP:0031188	Genital edema
HP:0031189	Wrist drop
HP:0031190	Superficial dermal perivascular inflammatory infiltrate
HP:0031191	Deep dermal perivascular inflammatory infiltrate
HP:0031192	Abnormal morphology of left ventricular trabeculae
HP:0031193	Abnormal morphology of right ventricular trabeculae
HP:0031194	Increased density of left ventricular trabeculae
HP:0031195	Apical hypertrabeculation of the left ventricle
HP:0031196	Thin myocardium compact layer
HP:0031197	Cellular urinary casts
HP:0031198	Renal tubular epithelial cell casts
HP:0031199	Acellular urinary casts
HP:0031200	Hyaline casts
HP:0031201	Granular casts
HP:0031202	Waxy casts
HP:0031203	Fatty casts
HP:0031204	Bacterial cell casts
HP:0031205	Reduced lysosomal acid lipase activity
HP:0031206	Striatal T2 hyperintensity
HP:0031207	Hepatic hemangioma
HP:0031208	Increased pituitary glycoprotein alpha subunit level
HP:0031209	Decreased lipoprotein lipase activity
HP:0031210	Abnormal circulating hyaluronic acid concentration
HP:0031211	Elevated cholesterol ester level
HP:0031212	Abnormal circulating progesterone level
HP:0031213	Elevated circulating 17-hydroxyprogesterone
HP:0031214	Decreased circulating dehydroepiandrosterone level
HP:0031215	Decreased circulating dehydroepiandrosterone-sulfate level
HP:0031216	Increased circulating progesterone
HP:0031217	Hot flashes
HP:0031218	Inappropriate antidiuretic hormone secretion
HP:0031219	Reduced radioactive iodine uptake
HP:0031220	Increased radioactive iodine uptake
HP:0031221	Abnormal radioactive iodine uptake test result
HP:0031222	Increased circulating thyroxine-binding globulin level
HP:0031223	Focal pancreatic islet hyperplasia
HP:0031224	Diffuse pancreatic islet hyperplasia
HP:0031225	Intrapulmonary shunt
HP:0031226	Perinephric fluid collection
HP:0031227	Nasopharyngeal teratoma
HP:0031228	Abnormal incisura morphology
HP:0031229	Increased incisura length
HP:0031230	Decreased incisura length
HP:0031231	Narrow incisura width
HP:0031232	Increased incisura width
HP:0031233	Horizontal inferior border of scapula
HP:0031234	Neutrophilic infiltration of the skin
HP:0031235	Predominantly epidermal neutrophilic infiltrate
HP:0031236	Predominantly dermal neutrophilic infiltrate
HP:0031237	Internally nucleated skeletal muscle fibers
HP:0031238	Necklace skeletal muscle fibers
HP:0031239	Extrafoveal choroidal neovascularization
HP:0031240	Juxtafoveal choroidal neovascularization
HP:0031241	Subfoveal choroidal neovascularization
HP:0031242	Decreased circulating chylomicron concentration
HP:0031243	Decreased VLDL cholesterol concentration
HP:0031244	Swollen lip
HP:0031245	Productive cough
HP:0031246	Nonproductive cough
HP:0031247	Whooping cough
HP:0031248	Palmar pruritus
HP:0031249	Parageusia
HP:0031250	Lip fissure
HP:0031251	Abnormal subclavian artery morphology
HP:0031252	Dilated left subclavian artery
HP:0031253	Anomalous origin of left subclavian artery
HP:0031254	Thalamic arteriovenous malformation
HP:0031255	Hypothalamic arteriovenous malformation
HP:0031256	Optic nerve arteriovenous malformation
HP:0031257	Arteriovenous malformation of the maxilla
HP:0031258	Delirium
HP:0031259	Oophoritis
HP:0031260	Triangular tibia
HP:0031261	Bladder polyp
HP:0031263	Abnormal renal corpuscle morphology
HP:0031264	Abnormal morphology of Bowman capsule
HP:0031265	Abnormal podocyte morphology
HP:0031266	Podocyte foot process effacement
HP:0031267	Abnormal CD69 upregulation upon TCR activation
HP:0031268	Decreased CD69 upregulation upon TCR activation
HP:0031269	Abnormal CD25 upregulation upon TCR activation
HP:0031270	Decreased CD25 upregulation upon TCR activation
HP:0031271	Absent ankle pulse
HP:0031272	Pulmonary arterial atherosclerosis
HP:0031273	Shock
HP:0031274	Hypovolemic shock
HP:0031275	Distributive shock
HP:0031276	Obstructive shock
HP:0031278	Abnormal thoracic duct morphology
HP:0031279	Abnormal response to gonadotropin-releasing hormone stimulation test
HP:0031280	Increased LH response to gonadotropin-releasing hormone stimulation test
HP:0031281	Sialadenitis
HP:0031282	Malalignment of the great toenail
HP:0031283	Tufted hairs
HP:0031284	Flushing
HP:0031285	Abnormal perifollicular morphology
HP:0031286	Perifollicular erythema
HP:0031287	Seborrheic keratosis
HP:0031288	Cobblestone-like hyperkeratosis
HP:0031289	White papule
HP:0031290	Tuberous xanthoma
HP:0031291	Ichthyosis follicularis
HP:0031292	Cutaneous abscess
HP:0031293	Digital pitting scar
HP:0031294	Hypoplastic right atrium
HP:0031295	Left atrial enlargement
HP:0031296	Atrial septal hypertrophy
HP:0031297	Unroofed coronary sinus
HP:0031298	Coronary sinus enlargement
HP:0031299	Elevated left atrial pressure
HP:0031300	Abnormal circulating properdin level
HP:0031301	Peripheral arterial calcification
HP:0031302	Lower extremity peripheral arterial calcification
HP:0031303	Femoral arterial calcification
HP:0031304	Iliac arterial calcification
HP:0031305	Tibial arterial calcification
HP:0031306	Intracranial arterial calcification
HP:0031307	Internal carotid artery calcification
HP:0031308	Vertebral artery calcification
HP:0031309	Cerebral artery calcification
HP:0031310	Basilar artery calcification
HP:0031311	Middle cerebral artery calcification
HP:0031313	Abdominal aortic calcification
HP:0031314	Carotid artery calcification
HP:0031315	External carotid artery calcification
HP:0031316	Abnormal ventricular myocardium morphology
HP:0031317	Fatty replacement of ventricular myocardial tissue
HP:0031318	Myofiber disarray
HP:0031319	Cardiomyocyte hypertrophy
HP:0031320	Cardiomyocyte mitochondrial proliferation
HP:0031321	Myocardial immune cell infiltration
HP:0031322	Myocardial lymphocytic infiltration
HP:0031323	Myocardial eosinophilic infiltration
HP:0031324	Myocardial multinucleated giant cells
HP:0031325	Myocardial granulomatous infiltrates
HP:0031326	Monoclonal light chain cardiac amyloidosis
HP:0031327	Transthyretin cardiac amyloidosis
HP:0031328	Perivascular cardiac fibrosis
HP:0031329	Interstitial cardiac fibrosis
HP:0031330	Perivascular myocardial immune cell infiltration
HP:0031331	Abnormal cardiomyocyte morphology
HP:0031332	Cardiomyocyte degeneration
HP:0031333	Myocardial sarcomeric disarray
HP:0031334	Cardiomyocyte inclusion bodies
HP:0031335	Abnormal cardiomyocyte mitochondrial morphology
HP:0031336	Intranuclear cardiomyocyte mitochondria
HP:0031337	Abnormal cardiomyocyte connexin43 staining
HP:0031338	Abnormal cardiomyocyte plakoglobin staining
HP:0031339	Abnormal cadiomyocyte dystrophin staining
HP:0031340	Abnormal lysosomal morphology
HP:0031341	Gastric arteriovenous malformation
HP:0031342	Duodenal arteriovenous malformation
HP:0031343	Jejunal arteriovenous malformation
HP:0031344	Pelvic arteriovenous malformation
HP:0031345	Colonic arteriovenous malformation
HP:0031346	Rectal arteriovenous malformation
HP:0031347	Uterine arteriovenous malformation
HP:0031348	Dextrotransposition of the great arteries
HP:0031349	Levotransposition of the great arteries
HP:0031350	Cardiac sarcoma
HP:0031351	Calcified amorphous tumor of the heart
HP:0031352	Chest tightness
HP:0031353	Otitis media with effusion
HP:0031354	Sleep onset Insomnia
HP:0031355	Maintenance insomnia
HP:0031356	Terminal insomnia
HP:0031357	Glomeruloid hemangioma
HP:0031358	Vegetative state
HP:0031359	Cutaneous sclerotic plaque
HP:0031360	Yellow skin plaque
HP:0031361	Zebra bodies
HP:0031362	Sex-limited autosomal recessive inheritance
HP:0031363	Palpable purpura
HP:0031364	Ecchymosis
HP:0031365	Macular purpura
HP:0031366	Palate neoplasm
HP:0031367	Metaphyseal striations
HP:0031368	Intestinal perforation
HP:0031369	Colon perforation
HP:0031370	Small intestinal perforation
HP:0031371	Rectal perforation
HP:0031372	Cold paresis
HP:0031373	Stiff tongue
HP:0031374	Ankle weakness
HP:0031375	Refractory
HP:0031377	Abnormal cell proliferation
HP:0031378	Abnormal lymphocyte proliferation
HP:0031379	Abnormal T cell proliferation
HP:0031380	Abnormal B cell proliferation
HP:0031381	Decreased lymphocyte proliferation in response to mitogen
HP:0031382	Decreased lymphocyte proliferation in response to anti-CD3
HP:0031383	Abnormal lymphocyte surface marker expression
HP:0031384	Reduced T cell CD40 expression
HP:0031385	Megakaryocyte nucleus hypolobulation
HP:0031386	Increased micromegakaryocyte count
HP:0031387	Increased multinucleated megakaryocyte count
HP:0031388	Megakaryocyte nucleus hyperlobulation
HP:0031389	Abnormal MHC II surface expression
HP:0031390	Reduced MHC II surface expression
HP:0031391	Elevated MHC II surface expression
HP:0031392	Abnormal proportion of CD4 T cells
HP:0031393	Abnormal proportion of CD8 T cells
HP:0031394	Abnormal CD4:CD8 ratio
HP:0031396	Abnormal proportion of naive T cells
HP:0031397	Reduced proportion of naive T cells
HP:0031398	Elevated proportion of naive T cells
HP:0031399	Abnormal proportion of double-negative alpha-beta regulatory T cell
HP:0031401	Reduced proportion of CD4-negative, CD8-negative, alpha-beta regulatory T cells
HP:0031402	Reduced antigen-specific T cell proliferation
HP:0031403	Impaired pathogen-specific CD8 cytoxicity
HP:0031404	Impaired antigen-specific response
HP:0031405	Poroma
HP:0031406	Abnormal cytokine signaling
HP:0031407	Impaired cytokine signaling
HP:0031408	Increased proportion of CD25+ mast cells
HP:0031409	Abnormal lymphocyte physiology
HP:0031410	Abnormal distribution of CD56 bright/dim natural killer cells
HP:0031411	Abnormal chromosome morphology
HP:0031412	Abnormal telomere morphology
HP:0031413	Short telomere length
HP:0031414	High serum calcifediol
HP:0031415	High serum calcitriol
HP:0031416	Abnormal nasal mucus secretion
HP:0031417	Rhinorrhea
HP:0031418	Increased body mass index
HP:0031419	Reduced sex -hormone binding protein level
HP:0031420	Small yellow foveal lesion with surrounding grey zone
HP:0031421	Small superior frontal cortex
HP:0031422	Abnormal morphology of the cerebellar cortex
HP:0031423	Small cerebellar cortex
HP:0031424	Abnormal circulating beta-C-terminal telopeptide level
HP:0031425	Increased circulating beta-C-terminal telopeptide level
HP:0031426	Decreased circulating beta-C-terminal telopeptide level
HP:0031427	Abnormal circulating osteocalcin level
HP:0031428	Increased circulating osteocalcin level
HP:0031429	Decreased circulating osteocalcin level
HP:0031430	Oligoclonal T cell expansion
HP:0031431	Persistent repetition of words
HP:0031432	Persistent repetition of actions
HP:0031433	Alexithymia
HP:0031434	Abnormal speech prosody
HP:0031435	Monotonic speech
HP:0031436	Increased pitch variability of speech
HP:0031437	Pregnancy exposure
HP:0031438	Abnormal sex hormone-binding globulin level
HP:0031439	Abnormal angiostatin level
HP:0031440	obsolete Abnormal tricuspid valve morphology
HP:0031441	Abnormal tricuspid valve annulus morphology
HP:0031442	Abnormal tricuspid chordae tendinae morphology
HP:0031443	Abnormal tricuspid valve leaflet morphology
HP:0031444	Dilatation of the tricuspid annulus
HP:0031445	Oral mucosa nodule
HP:0031446	Erosion of oral mucosa
HP:0031447	Penile freckling
HP:0031448	Herpetiform vesicles
HP:0031449	Perineal hemangioma
HP:0031450	Polycyclic
HP:0031451	Lower extremity subcutanous fat hypertrophy
HP:0031452	Lichenoid skin lesion
HP:0031453	Oral lichenoid lesion
HP:0031454	Apocrine hidrocystoma
HP:0031455	Presacral ganglioneuroma
HP:0031456	Ectopic pregnancy
HP:0031457	Pulmonary opacity
HP:0031458	Adenoiditis
HP:0031459	Soft tissue neoplasm
HP:0031460	Benign muscle neoplasm
HP:0031461	Intramuscular Myxoma
HP:0031462	Musculotendinous retraction
HP:0031463	Esophageal squamous papilloma
HP:0031464	Genital blistering
HP:0031465	Abnormal vasa vasorum morphology
HP:0031466	Impairment in personality functioning
HP:0031467	Negative affectivity
HP:0031468	Separation insecurity
HP:0031469	Low self esteem
HP:0031472	Risk taking
HP:0031473	Hostility
HP:0031474	Pulmonary chondroma
HP:0031475	Nonconvulsive status epilepticus
HP:0031476	Abnormal buccal mucosa cell morphology
HP:0031477	obsolete Abnormal mitral valve morphology
HP:0031478	Abnormal mitral valve annulus morphology
HP:0031479	Dilatation of the mitral annulus
HP:0031480	Abnormal mitral valve leaflet morphology
HP:0031481	Abnormal mitral valve physiology
HP:0031482	Abnormal regional left ventricular contraction
HP:0031483	Reduced contraction of the left ventricular apex
HP:0031484	Cold-induced hemolysis
HP:0031485	Subperiosteal bone formation
HP:0031486	Vascular malformation of the lip
HP:0031487	Capillary malformation of the lip
HP:0031488	Arteriovenous malformation of the lip
HP:0031489	Venous malformation of the lip
HP:0031490	Hemangioma of the lip
HP:0031491	Continuous spike and waves during slow sleep
HP:0031492	Epithelial neoplasm
HP:0031493	Glandular cell neoplasm
HP:0031494	Ovarian mucinous tumor
HP:0031495	Mucinous neoplasm
HP:0031496	Mucinous cystic neoplasm of the pancreas
HP:0031497	Mucinous colorectal carcinoma
HP:0031498	Mucinous gastric carcinoma
HP:0031499	Appendiceal mucinous neoplasm
HP:0031500	Abdominal mass
HP:0031501	Pelvic mass
HP:0031502	Trophoblastic tumor
HP:0031503	Night gasping
HP:0031504	Foamy urine
HP:0031505	Abnormal circulating thyroxine level
HP:0031506	Increased circulating thyroxine level
HP:0031507	Decreased circulating thyroxine level
HP:0031508	Abnormal thyroid hormone level
HP:0031509	Dry nipple
HP:0031510	Linear earlobe crease
HP:0031511	Diagonal earlobe crease
HP:0031512	Abnormal cutaneous collagen fibril morphology
HP:0031513	Luse bodies
HP:0031514	Increased proportion of exhausted T cells
HP:0031515	Abnormal meiosis
HP:0031516	Oocyte arrest at metaphase I
HP:0031517	Verruciform xanthoma
HP:0031518	Absent posterior alpha rhythm
HP:0031519	Cauliflower deformity of dermal collagen fibrils
HP:0031520	Groin pain
HP:0031521	Vaginal clear cell adenocarcinoma
HP:0031522	Cervical clear cell adenocarcinoma
HP:0031523	Salivary gland oncocytoma
HP:0031524	Ampulla of Vater carcinoma
HP:0031525	Keratoacanthoma
HP:0031526	Subretinal fluid
HP:0031527	Intraretinal fluid
HP:0031528	Subretinal deposits
HP:0031529	Focal subretinal deposits
HP:0031530	Multifocal subretinal deposits
HP:0031531	Sub-RPE deposits
HP:0031532	Focal sub-RPE deposits
HP:0031533	Multifocal sub-RPE deposits
HP:0031534	Passive dorsiflexion of the 5th finger more than 90 degrees
HP:0031535	Increased theta frequency activity in EEG
HP:0031536	Separate origin of the left anterior descending and left circumflex artery
HP:0031537	Anomalous origin of the left circumflex artery from the right coronary artery
HP:0031538	Abnormal dermoepidermal junction morphology
HP:0031539	Linear IgA deposits along the epidermal basement membrane zone
HP:0031540	Linear IgG deposits along the epidermal basement membrane zone
HP:0031541	Linear C3 deposits along the epidermal basement membrane zone
HP:0031542	Myelin-like whorls in vacuolated fibers
HP:0031544	Elevated propionylcarnitine level
HP:0031545	Abnormally low T cell receptor excision circle level
HP:0031546	Cardiac conduction abnormality
HP:0031547	Abnormal QT interval
HP:0031548	Follicular infundibulum tumor
HP:0031549	Lymphocytoma cutis
HP:0031550	Abnormal flow cytometry test rest
HP:0031551	Reduced cell surface marker level
HP:0031552	Reduced fibroblast surface marker level
HP:0031553	Reduced granulocyte surface marker level
HP:0031554	Reduced granulocyte CD55 level
HP:0031555	Reduced granulocyte CD59 level
HP:0031556	Reduced granulocyte CD16 level
HP:0031557	Reduced fibroblast CD55 level
HP:0031558	Reduced fibroblast CD59 level
HP:0031559	Reduced fibroblast CD16 level
HP:0031560	Coronary cameral fistula
HP:0031561	Coronary cameral fistula to right ventricle
HP:0031562	Balanced double aortic arch
HP:0031563	Coronary arteriovenous fistula
HP:0031564	Bronchial isomerism
HP:0031565	Abdominal situs ambiguus
HP:0031566	Abnormal pulmonary valve cusp morphology
HP:0031567	Abnormal aortic valve cusp morphology
HP:0031568	Thickened aortic valve cusp
HP:0031569	Absent aortic valve cusps
HP:0031570	Tessier number 0 facial cleft
HP:0031571	Paramedian facial cleft
HP:0031572	Tessier number 1 facial cleft
HP:0031573	Tessier number 2 facial cleft
HP:0031574	Orbital cleft
HP:0031575	Tessier number 3 facial cleft
HP:0031576	Tessier number 4 facial cleft
HP:0031577	Tessier number 5 facial cleft
HP:0031578	Tessier number 6 facial cleft
HP:0031579	Tessier number 7 facial cleft
HP:0031580	Tessier number 8 facial cleft
HP:0031581	Tessier number 9 facial cleft
HP:0031582	Tessier number 10 facial cleft
HP:0031583	Tessier number 11 facial cleft
HP:0031584	Tessier number 12 facial cleft
HP:0031585	Tessier number 13 facial cleft
HP:0031586	Tessier number 14 facial cleft
HP:0031587	Tessier number 30 facial cleft
HP:0031588	Unhappy demeanor
HP:0031589	Suicidal ideation
HP:0031590	Asthenopia
HP:0031591	Enlarged Eustachian valve
HP:0031592	Situs inversus with levocardia
HP:0031593	Abnormal PR interval
HP:0031594	PR segment depression
HP:0031595	Abnormal P wave
HP:0031596	Abnormal PR segment
HP:0031597	PR segment elevation
HP:0031598	Notched P wave
HP:0031599	P mitrale
HP:0031600	P wave inversion
HP:0031601	P pulmonale
HP:0031602	Abnormal mucociliary clearance
HP:0031603	Impaired nasal mucociliary clearance
HP:0031604	Agenesis of the carotid canal
HP:0031605	Abnormality of fundus pigmentation
HP:0031606	Retinal cotton wool spot
HP:0031607	Pelvic organ prolapse
HP:0031609	Geographic atrophy
HP:0031610	Recurrent shoulder dislocation
HP:0031611	Sub-inner limiting membrane hemorrhage
HP:0031613	Inferior chorioretinal coloboma
HP:0031614	Inferior retinal coloboma
HP:0031615	Hypopyon
HP:0031616	Anterior chamber flare
HP:0031618	Anterior chamber flare grade 1+
HP:0031619	Anterior chamber flare grade 2+
HP:0031620	Anterior chamber flare grade 3+
HP:0031621	Anterior chamber flare grade 4+
HP:0031622	Brown anomaly
HP:0031623	Brow ptosis
HP:0031624	Moderate myopia
HP:0031625	Pseudoaneurysm
HP:0031626	Coronary ostial atresia
HP:0031627	Globus pallidus calcification
HP:0031628	Aborted sudden cardiac death
HP:0031629	Impaired tandem gait
HP:0031630	Abnormal subpleural morphology
HP:0031631	Subpleural honeycombing
HP:0031632	Anomalous origin of the right subclavian artery from the descending aorta
HP:0031633	Isolation of the left subclavian artery
HP:0031634	Anomalous origin of the left common carotid artery from the main pulmonary artery
HP:0031635	Anomalous origin of the left common carotid artery from the brachiocephalic artery
HP:0031636	Anomalous origin of the right common carotid artery from the aorta
HP:0031637	Right coronary artery ostial atresia
HP:0031638	Anomalous origin of the left anterior descending artery from the pulmonary artery
HP:0031639	Absent left main coronary artery
HP:0031640	Abnormal radial artery morphology
HP:0031643	Fusiform ascending tubular aorta aneurysm
HP:0031644	Fusiform abdominal aortic aneurysm
HP:0031645	Saccular abdominal aortic aneurysm
HP:0031646	Fusiform aortic arch aneurysm
HP:0031647	Saccular aortic arch aneurysm
HP:0031648	Penetrating aortic ulcer
HP:0031649	Aortic rupture
HP:0031650	Abnormal atrioventricular valve physiology
HP:0031651	Abnormal tricuspid valve physiology
HP:0031652	Abnormal aortic valve physiology
HP:0031653	Abnormal heart valve physiology
HP:0031654	Abnormal pulmonary valve physiology
HP:0031655	Quadricuspid aortic valve
HP:0031656	Systolic anterior motion of the mitral valve
HP:0031657	Abnormal heart sound
HP:0031658	Third heart sound
HP:0031659	Fourth heart sound
HP:0031660	Loud first heart sound
HP:0031661	Abnormal second heart sound
HP:0031662	Fixed splitting of the second heart sound
HP:0031663	Paradoxical splitting of the second heart sound
HP:0031664	Systolic heart murmur
HP:0031665	Midsystolic murmur
HP:0031666	Late systolic murmur
HP:0031667	Holosystolic murmur
HP:0031668	Diastolic heart murmur
HP:0031669	Middiastolic murmur
HP:0031670	Continuous heart murmur
HP:0031671	Typical atrial flutter
HP:0031672	Reverse typical atrial flutter
HP:0031673	Orthodromic atrioventricular reentrant tachycardia
HP:0031674	Antidromic atrioventricular reentrant tachycardia
HP:0031675	Fascicular left ventricular tachycardia
HP:0031676	Monomorphic ventricular tachycardia
HP:0031677	Polymorphic ventricular tachycardia
HP:0031678	Atherosclerotic lesion
HP:0031679	Type I atherosclerotic lesion
HP:0031680	Type II atherosclerotic lesion
HP:0031681	Type III atherosclerotic lesion
HP:0031682	Type V atherosclerotic lesion
HP:0031683	Type VI atherosclerotic lesion
HP:0031684	Renal artery atherosclerosis
HP:0031685	Abnormal stool composition
HP:0031686	Increased stool alpha1-antitrypsin concentration
HP:0031687	Abnormally loud pulmonic component of the second heart sound
HP:0031688	Erythroid dysplasia
HP:0031689	Megakaryocyte dysplasia
HP:0031690	Opportunistic infection
HP:0031691	Severe viral infection
HP:0031692	Severe cytomegalovirus infection
HP:0031693	Severe Epstein Barr virus infection
HP:0031694	Severe adenovirus infection
HP:0031695	Severe parainfluenza infection
HP:0031696	Disseminated viral infection
HP:0031697	Disseminated infection with live vaccine virus
HP:0031698	Disseminated Bacillus Calmette-Guerin infection
HP:0031699	Disseminated cryptosporidium infection
HP:0031700	Invasive parasitic infection
HP:0031701	Anterior chamber inflammatory cells
HP:0031702	Anterior chamber red blood cells
HP:0031703	Abnormal ear morphology
HP:0031704	Abnormal ear physiology
HP:0031705	Compensatory head posture
HP:0031706	Compensatory chin depression
HP:0031707	Compensatory face turn to the right
HP:0031708	Compensatory face turn to the left
HP:0031709	Compensatory head tilt to the right shoulder
HP:0031710	Compensatory head tilt to the left shoulder
HP:0031711	Asymmetric abdominal aortic aneurysm
HP:0031713	Constant exotropia
HP:0031714	Distance exotropia
HP:0031715	Near exotropia
HP:0031716	Cyclic exotropia
HP:0031717	Alternating exotropia
HP:0031718	Consecutive exotropia
HP:0031719	True distance exotropia
HP:0031720	Simulated distance exotropia
HP:0031721	Sensory exotropia
HP:0031722	Near esotropia
HP:0031723	Secondary esotropia
HP:0031724	Microtropia
HP:0031725	Hypophoria
HP:0031726	Incyclotropia
HP:0031727	Excyclotropia
HP:0031728	Mild hypermetropia
HP:0031729	Moderate hypermetropia
HP:0031730	Axial myopia
HP:0031731	Increased tear production
HP:0031732	Increased basal tear production
HP:0031733	Reflex tearing
HP:0031734	Lacrimal pump failure
HP:0031736	Involutional entropion
HP:0031737	Cicatricial entropion
HP:0031738	Mechanical entropion
HP:0031739	Abnormal oblique muscle physiology
HP:0031740	Abnormal horizontal rectus muscle physiology
HP:0031741	Inferior oblique muscle underaction
HP:0031742	Inferior rectus muscle underaction
HP:0031743	Inferior rectus muscle overaction
HP:0031744	Superior rectus muscle weakness
HP:0031745	Superior rectus muscle overaction
HP:0031746	Superior rectus muscle rescriction
HP:0031747	Superior rectus muscle underaction
HP:0031748	Abnormal vertical rectus muscle physiology
HP:0031749	Abnormal lateral rectus muscle physiology
HP:0031750	Lateral rectus muscle weakness
HP:0031751	Lateral rectus muscle underaction
HP:0031752	Lateral rectus muscle overaction
HP:0031753	Medial rectus muscle weakness
HP:0031754	Medial rectus muscle overaction
HP:0031755	Abnormal rectus muscle physiology
HP:0031756	Medial rectus muscle underaction
HP:0031757	Medial rectus muscle restriction
HP:0031758	Lateral rectus muscle restriction
HP:0031759	Basic constant esotropia
HP:0031760	Non-accomodative esotropia
HP:0031761	Infantile constant esotropia
HP:0031762	Distance esotropia
HP:0031763	Cyclic esotropia
HP:0031764	Fully accomodative esotropia
HP:0031765	Partially accomodative esotropia
HP:0031766	Convergence excess esotropia
HP:0031767	Consecutive esotropia
HP:0031768	Parafoveal fixation
HP:0031769	Peripheral fixation
HP:0031770	Epicanthus palpebralis
HP:0031771	Epicanthus tarsalis
HP:0031772	Abnormal posterior circulating artery morphology
HP:0031773	Posterior communicating artery aneurysm
HP:0031774	Posterior communicating artery infundibulum
HP:0031775	Neurogenic strabismus
HP:0031776	Cyclotropia
HP:0031777	Cyclophoria
HP:0031778	Incyclophoria
HP:0031779	Excyclophoria
HP:0031780	Eosinophilic ascites
HP:0031781	Microtropia with identity
HP:0031782	Microtropia without identity
HP:0031783	Absent coronary sinus
HP:0031784	Abnormal ascending aorta morphology
HP:0031785	Abnormal eyelid movement
HP:0031786	Cogan lid twitch
HP:0031787	Oblique astigmatism
HP:0031788	With the rule astigmatism
HP:0031789	Against the rule astigmatism
HP:0031790	Mixed astigmatism
HP:0031791	Lenticular astigmatism
HP:0031792	Irregular astigmatism
HP:0031793	Increased serum leptin
HP:0031794	Decreased circulating glycerol level
HP:0031795	Abnormal circulating glycerol level
HP:0031796	Recurrent
HP:0031797	Clinical course
HP:0031798	Elevated apolipoprotein B level
HP:0031799	Decreased apolipoprotein AI level
HP:0031800	Elevated apolipoprotein A-II level
HP:0031801	Vocal cord dysfunction
HP:0031803	Fundus hemorrhage
HP:0031804	Premacular hemorrhage
HP:0031805	Intraretinal hemorrhage
HP:0031806	Abnormal basophil count
HP:0031807	Increased basophil count
HP:0031808	Decreased basophil count
HP:0031809	Archibald's sign
HP:0031810	Anti-ganglioside antibody positivity
HP:0031811	Bilirubinuria
HP:0031812	Nitrituria
HP:0031813	Colonic eosinophilia
HP:0031814	Palilalia
HP:0031815	Abnormal oral physiology
HP:0031816	Abnormal oral morphology
HP:0031817	Decreased circulating parathyroid hormone level
HP:0031818	Abnormal waist to hip ratio
HP:0031819	Increased waist to hip ratio
HP:0031820	Decreased waist to hip ratio
HP:0031821	Abnormal hypoxanthine-guanine phosphoribosyltransferase level
HP:0031822	Elevated hypoxanthine-guanine phosphoribosyltransferase level
HP:0031823	Reduced hypoxanthine-guanine phosphoribosyltransferase level
HP:0031824	Hepatic mastocytosis
HP:0031825	Freezing of gait
HP:0031826	Abnormal reflex
HP:0031827	Absent abdominal reflex
HP:0031828	Abnormal superficial reflex
HP:0031829	Absent cremaster reflex
HP:0031830	Pinguecula
HP:0031831	Decreased serum zinc
HP:0031832	Hypermetric downward saccades
HP:0031833	Hypometric upward saccades
HP:0031834	Aortopulmonary collateral arteries
HP:0031835	Abnormal superoxide dismutase activity
HP:0031836	Increased superoxide dismutase activity
HP:0031837	Decreased superoxide dismutase activity
HP:0031838	Presence of xenobiotic
HP:0031840	Urine xenobiotic
HP:0031841	Positive urine methadone test
HP:0031842	Lymphangiectasis
HP:0031843	Bradyphrenia
HP:0031844	Euphoria
HP:0031845	Abnormal libido
HP:0031846	Femur fracture
HP:0031847	Difficulty walking backward
HP:0031848	Cock-walk gait
HP:0031849	Sleep-wake inversion
HP:0031850	Abnormal hematocrit
HP:0031851	Reduced hematocrit
HP:0031853	Isomerism
HP:0031854	Left Isomerism
HP:0031855	Right isomerism
HP:0031856	Hobby horse gait
HP:0031857	Ineffective esophageal peristalsis
HP:0031858	Esophageal furrows
HP:0031860	Abnormal heart rate variability
HP:0031861	Decreased heart rate variability
HP:0031862	Increased heart rate variability
HP:0031863	Bloodstream infectious agent
HP:0031864	Bacteremia
HP:0031865	Abnormal liver physiology
HP:0031866	Clasp-knife sign
HP:0031867	Neck hypertonia
HP:0031868	Optic ataxia
HP:0031869	Recurrent joint dislocation
HP:0031870	Phosphohydroxylysinuria
HP:0031871	Abnormal Langerhans cell morphology
HP:0031872	Absent Birbeck granules in Langerhans cells
HP:0031873	Early chronotype
HP:0031874	Late chronotype
HP:0031875	Abnormal hepcidin level
HP:0031876	Decreased hepcidin level
HP:0031877	Elevated hepcidin level
HP:0031878	Acromicria
HP:0031879	Abnormal eyelid physiology
HP:0031880	Eyelid laxity
HP:0031881	Decreased tear drainage
HP:0031882	Agyria
HP:0031883	Increased proinsulin:insulin ratio
HP:0031884	Abnormal CSF glucose level
HP:0031885	Hyperglycorrhachia
HP:0031886	Abnormal LDL cholesterol concentration
HP:0031887	Abnormal chylomicron concentration
HP:0031888	Abnormal HDL cholesterol concentration
HP:0031889	Abnormal VLDL cholesterol concentration
HP:0031890	Increased urine urobilinogen
HP:0031891	Decreased eosinophil count
HP:0031898	Rouleaux formation
HP:0031899	Abnormal coagulation factor V activity
HP:0031900	Abnormal serum mast cell beta-tryptase concentration
HP:0031901	Increased serum mast cell beta-tryptase concentration
HP:0031902	Decreased serum mast cell beta-tryptase concentration
HP:0031903	Abnormal serum selenium concentration
HP:0031904	Abnormal total hemolytic complement activity
HP:0031905	Increased total hemolytic complement activity
HP:0031906	Decreased total hemolytic complement activity
HP:0031907	Anti-mitochondrial M2 antibody positivity
HP:0031908	Micrographia
HP:0031909	Unicornuate uterus
HP:0031910	Abnormal cranial nerve physiology
HP:0031911	Abnormal fifth cranial nerve physiology
HP:0031912	Trigeminal anesthesia
HP:0031913	Rhombencephalosynapsis
HP:0031914	Fluctuating
HP:0031915	Stable
HP:0031917	Digital ulcer
HP:0031918	Ovarian sex cord-stromal tumor
HP:0031919	Juvenile type ovarian granulosa cell tumor
HP:0031920	Malignant ovarian granulosa cell tumor
HP:0031921	Gastrocnemius myalgia
HP:0031922	Renal artery duplication
HP:0031923	Hematocolpos
HP:0031924	Rope sign
HP:0031925	Rosette
HP:0031926	Homer Wright rosette
HP:0031927	Flexner-Wintersteiner rosette
HP:0031928	True ependymal rosette
HP:0031929	Perivascular pseudorosette
HP:0031930	Neurocytic rosette
HP:0031931	Ocular flutter
HP:0031932	Aorto-left ventricular tunnel
HP:0031933	Aorto-right ventricular tunnel
HP:0031934	Abnormal descending aorta morphology
HP:0031935	Ascending aorta hypoplasia
HP:0031936	Delayed ability to walk
HP:0031937	Tachylalia
HP:0031938	Abnormal conus terminalis morphology
HP:0031939	Conus terminalis arteriovenous malformation
HP:0031941	Abnormal portal venous system morphology
HP:0031942	Congenital absence of portal vein
HP:0031943	Akathisia
HP:0031944	Pleural thickening
HP:0031945	Elevated N,N-dimethylglycine level
HP:0031946	Elevated urinary N,N-dimethylglycine level
HP:0031947	Tongue tremor
HP:0031948	Snowball lesion of corpus callosum
HP:0031949	Recurrent bacterial upper respiratory tract infections
HP:0031950	Usual interstitial pneumonia
HP:0031951	Nocturnal seizures
HP:0031952	Neurogenic claudication
HP:0031953	Cautious gait
HP:0031954	Dystonic gait
HP:0031955	Antalgic gait
HP:0031956	Elevated serum aspartate aminotransferase
HP:0031957	Spastic hemiparetic gait
HP:0031958	Spastic paraparetic gait
HP:0031959	Leg dystonia
HP:0031960	Arm dystonia
HP:0031961	Abnormal serum anion gap
HP:0031962	Elevated serum anion gap
HP:0031963	Decreased serum anion gap
HP:0031964	Elevated serum alanine aminotransferase
HP:0031965	Increased RBC distribution width
HP:0031967	Cloudy urine
HP:0031969	Reduced blood urea nitrogen
HP:0031970	Abnormal blood urea nitrogen
HP:0031971	Subaortic ventricular septal bulge
HP:0031972	Presyncope
HP:0031973	Increased vertical cup-to-disc ratio
HP:0031974	Increased vertical cup-to-disc ratio - 0.6
HP:0031975	Increased vertical cup-to-disc ratio - 0.7
HP:0031976	Increased vertical cup-to-disc ratio - 0.8
HP:0031977	Increased vertical cup-to-disc ratio - 0.9
HP:0031978	Increased vertical cup-to-disc ratio - 1.0
HP:0031979	Abnormal urine carbohydrate level
HP:0031980	Abnormal urine carboxylic acid level
HP:0031981	Elevated urine glycolate
HP:0031982	Abnormal putamen morphology
HP:0031983	Abnormal chest radiograph finding (lung)
HP:0031984	Esophageal food impaction
HP:0031985	Esophageal exudate
HP:0031986	Polyminimyoclonus
HP:0031987	Diminished ability to concentrate
HP:0031988	Muscle spasm
HP:0031989	Perioral spasm
HP:0031990	Chvostek sign
HP:0031991	Increased urinary excretion of galactosyl hydroxylysine
HP:0031992	Apical hypertrophic cardiomyopathy
HP:0031993	Hoffmann sign
HP:0031994	Bronchial breath sound
HP:0031995	Squawks
HP:0031996	Inspiratory crackles
HP:0031997	Early inspiratory crackles
HP:0031998	Late inspiratory crackles
HP:0031999	Expiratory crackles
HP:0032000	Pleural rub
HP:0032001	Pink urine
HP:0032002	Orange urine
HP:0032003	Green urine
HP:0032004	Pruritus vulvae
HP:0032005	Hemidystonia
HP:0032006	Lip tremor
HP:0032007	Maceration
HP:0032008	Pulmonary fat embolism
HP:0032009	Infantile constant exotropia
HP:0032010	Basic constant exotropia
HP:0032011	Heterophoria
HP:0032012	Heterotropia
HP:0032013	Hypermetric horizontal saccades
HP:0032014	Dysmetric vertical saccades
HP:0032015	Dysmetric horizontal saccades
HP:0032016	Abnormal sputum
HP:0032017	Sputum eosinophilia
HP:0032018	Multiple mononeuropathy
HP:0032019	Muscle eosinophilia
HP:0032020	Eosinophilic bladder infiltration
HP:0032021	Eosinophilic liver infiltration
HP:0032022	Eosinophilic dermal infiltration
HP:0032023	Eosinophilic gallbladder infiltration
HP:0032024	Ileal ulcer
HP:0032025	Reduced serum alpha-1-antitrypsin
HP:0032026	Anetoderma
HP:0032027	Retinal dots
HP:0032028	Macular dots
HP:0032029	Floppy eyelid
HP:0032030	Lateral canthal tendon laxity
HP:0032031	Medial canthal tendon laxity
HP:0032032	Horizontal eyelid laxity
HP:0032033	Vertical eyelid laxity
HP:0032034	Upper eyelid laxity
HP:0032035	Lower eyelid laxity
HP:0032036	Abnormal contrast sensitivity
HP:0032037	Mildly reduced visual acuity
HP:0032039	Abnormality of the ocular adnexa
HP:0032040	Abnormal ocular adnexa physiology
HP:0032041	Vocal cord polyp
HP:0032043	Odynophagia
HP:0032044	Decreased vigilance
HP:0032045	Hypoplastic carotid canal
HP:0032046	Focal cortical dysplasia
HP:0032047	Focal cortical dysplasia type I
HP:0032048	Focal cortical dysplasia type Ia
HP:0032049	Focal cortical dysplasia type Ib
HP:0032050	Focal cortical dysplasia type Ic
HP:0032051	Focal cortical dysplasia type II
HP:0032052	Focal cortical dysplasia type IIa
HP:0032053	Focal cortical dysplasia type IIb
HP:0032054	Focal cortical dysplasia type III
HP:0032055	Focal cortical dysplasia type IIIa
HP:0032056	Focal cortical dysplasia type IIIb
HP:0032057	Focal cortical dysplasia type IIIc
HP:0032058	Focal cortical dysplasia type IIId
HP:0032059	Mild malformation of cortical development
HP:0032060	Epithelioid hemangioma
HP:0032061	Hypereosinophilia
HP:0032062	Mallory-Weiss tear
HP:0032063	Ankle joint effusion
HP:0032064	Gastrointestinal eosinophilia
HP:0032065	Abnormal serum bicarbonate concentration
HP:0032066	Decreased serum bicarbonate concentration
HP:0032067	Elevated serum bicarbonate concentration
HP:0032068	Increased urinary mucus
HP:0032069	Anti-thyroglobulin antibody positivity
HP:0032070	Leptomeningeal enhancement
HP:0032071	Pulmonary eosinophilic infiltration
HP:0032072	Popliteal synovial cyst
HP:0032073	Aplasia of the fallopian tube
HP:0032075	Splenopancreatic fusion
HP:0032076	Abnormal male urethral meatus morphology
HP:0032077	Male urethral meatus stenosis
HP:0032078	Angel-shaped phalanx
HP:0032079	Medial degeneration
HP:0032081	Intralamellar mucoid extracellular matrix accumulation
HP:0032082	Translamellar mucoid extracellular matrix accumulation
HP:0032083	Aortic elastic fiber fragmentation
HP:0032084	Aortic elastic fiber thinning
HP:0032085	Aortic elastic fiber disorganization
HP:0032086	Aortic smooth muscle cell nuclei loss
HP:0032087	Aortic laminar medial collapse
HP:0032088	Aortic smooth muscle cell disorganization
HP:0032089	Aortic medial fibrosis
HP:0032090	Intralamellar aortic medial fibrosis
HP:0032091	Translamellar aortic medial fibrosis
HP:0032092	Left ventricular outflow tract obstruction
HP:0032094	Increased circulating surfactant protein level
HP:0032096	Abnormal manganese concentration
HP:0032097	Hypermanganesemia
HP:0032098	Hypomanganesemia
HP:0032099	Perioral radial furrowing
HP:0032100	Abnormal doll's eye reflex
HP:0032101	Unusual infection
HP:0032102	Wilson sign
HP:0032104	Saccadic oscillation
HP:0032105	Macrosaccadic oscillations
HP:0032106	Conjunctival icterus
HP:0032107	Limbal stem cell deficiency
HP:0032108	Mildly reduced contrast sensitivity
HP:0032109	Moderately reduced contrast sensitivity
HP:0032110	Severely reduced contrast sensitivity
HP:0032111	Abnormal Vistech contrast sensitivity test
HP:0032112	Abnormal Pelli Robson contrast sensitivity chart test
HP:0032113	Semidominant mode of inheritance
HP:0032114	Saccadic intrusion
HP:0032116	Macrosquare-wave jerks
HP:0032117	Macrosaccadic oscillation
HP:0032118	Retinitis
HP:0032119	Narrow angle glaucoma
HP:0032120	Abnormal peripheral nervous system physiology
HP:0032121	Froment sign
HP:0032122	Very low visual acuity
HP:0032123	Ultra-low vision
HP:0032124	Abnormal proportion of non-class-switched memory B cells
HP:0032125	Increased proportion of non-class-switched memory B cells
HP:0032126	Decreased proportion of non-class-switched memory B cells
HP:0032127	Abnormal plasmablast proportion
HP:0032128	Increased proportion of plasmablasts
HP:0032129	Decreased proportion of plasmablasts
HP:0032130	Mycobacterium abscessus abscessus infection
HP:0032131	Cervical dysplasia
HP:0032132	Decreased circulating total IgG
HP:0032133	Transient decreased circulating total IgG
HP:0032134	Chronic decreased circulating total IgG
HP:0032135	Decreased circulating IgG subclass level
HP:0032136	Decreased circulating IgG1 level
HP:0032137	Decreased circulating IgG3 level
HP:0032138	Decreased circulating IgG4 level
HP:0032139	Reduced isohemagglutinin level
HP:0032140	Decreased specific antibody response to vaccination
HP:0032141	Precordial pain
HP:0032142	Fetor hepaticus
HP:0032143	Burning mouth
HP:0032144	Coffee ground vomitus
HP:0032145	Sural nerve atrophy
HP:0032146	HbC hemoglobin
HP:0032147	Erythromelalgia
HP:0032148	Episodic pain
HP:0032149	Breakthrough pain
HP:0032150	Paroxysmal rectal pain
HP:0032151	Episodic eosinophilia
HP:0032152	Keratosis pilaris
HP:0032153	Joint subluxation
HP:0032154	Aphthous ulcer
HP:0032155	Abdominal cramps
HP:0032156	Skin detachment
HP:0032157	Recurrent genital herpes
HP:0032158	Unusual infection by anatomical site
HP:0032159	Fungal meningitis
HP:0032160	Cryptococcal meningitis
HP:0032161	Coccidioidal meningitis
HP:0032162	Unusual skin infection
HP:0032163	Molluscum contagiosum
HP:0032164	Increased blood folate concentration
HP:0032165	Placental mesenchymal dysplasia
HP:0032166	Unusual gastrointestinal infection
HP:0032167	Clostridium difficile enteritis
HP:0032168	Clostridium difficile colitis
HP:0032169	Severe infection
HP:0032170	Severe varicella zoster infection
HP:0032171	Bladder pain
HP:0040004	Abnormality of corneal shape
HP:0040006	Mortality/Aging
HP:0040007	Absent pigmentation of chest
HP:0040008	Aplasia of facial bones
HP:0040009	Hyperparakeratosis
HP:0040010	Small posterior fossa
HP:0040011	Flat posterior fossa
HP:0040012	Chromosome breakage
HP:0040013	Decreased mitochondrial number
HP:0040014	Increased mitochondrial number
HP:0040015	Increased activity of mitochondrial respiratory chain
HP:0040016	Prominent coccyx
HP:0040017	Protruding coccyx
HP:0040018	Clinodactyly of hallux
HP:0040019	Finger clinodactyly
HP:0040020	Radial deviation of the 5th finger
HP:0040021	Radial deviation of the thumb
HP:0040022	Clinodactyly of the 2nd finger
HP:0040023	Clinodactyly of the thumb
HP:0040024	Clinodactyly of the 3rd finger
HP:0040025	Clinodactyly of the 4th finger
HP:0040030	Chorioretinal hypopigmentation
HP:0040031	Chorioretinal hyperpigmentation
HP:0040032	Hypoplasia of the upper eyelids
HP:0040033	Aplasia/Hypoplasia of the fifth metatarsal bone
HP:0040034	Abnormality of the second metatarsal bone
HP:0040035	Abnormality of the fourth metatarsal bone
HP:0040036	Onychogryposis of fingernail
HP:0040037	obsolete Thin fingernail (obsolete)
HP:0040038	obsolete Thin toenail
HP:0040039	Onycholysis of fingernails
HP:0040040	Onycholysis of toenails
HP:0040042	Aplasia of the eccrine sweat glands
HP:0040043	Hypoplasia of the eccrine sweat glands
HP:0040044	Hypoplasia of the diaphragm
HP:0040045	Abnormality of the hemidiaphragms
HP:0040046	Abnormality of the left hemidiaphragm
HP:0040047	Abnormality of the right hemidiaphragm
HP:0040048	Aplasia of the left hemidiaphragm
HP:0040049	Macular edema
HP:0040050	Sparse upper eyelashes
HP:0040051	Abnormality of upper eyelashes
HP:0040052	Abnormality of lower eyelashes
HP:0040053	Long lower eyelashes
HP:0040054	Short upper eyelashes
HP:0040055	Short lower eyelashes
HP:0040056	Absent upper eyelashes
HP:0040057	Abnormality of nasal hair
HP:0040059	Calcification of ribs
HP:0040061	Osteosclerosis of the radius
HP:0040062	Slender radius
HP:0040063	Decreased adipose tissue
HP:0040064	Abnormality of limbs
HP:0040065	Abnormal morphology of bones of the upper limbs
HP:0040066	Abnormal morphology of bones of the lower limbs
HP:0040068	Abnormality of limb bone
HP:0040069	Abnormality of lower limb bone
HP:0040070	Abnormality of upper limb bone
HP:0040071	Abnormal morphology of ulna
HP:0040072	Abnormality of forearm bone
HP:0040073	Abnormal forearm bone morphology
HP:0040075	Hypopituitarism
HP:0040077	Abnormal concentration of calcium in blood
HP:0040078	Axonal degeneration
HP:0040079	Irregular dentition
HP:0040080	Anteverted ears
HP:0040081	Abnormal levels of creatine kinase in blood
HP:0040082	Happy demeanor
HP:0040083	Toe walking
HP:0040084	Abnormal circulating renin
HP:0040085	Abnormal circulating aldosterone
HP:0040086	Abnormal prolactin level
HP:0040087	Abnormal blood folate concentration
HP:0040088	Abnormal lymphocyte count
HP:0040089	Abnormal natural killer cell count
HP:0040090	Abnormality of the tympanic membrane
HP:0040091	Asymmetry of the size of ears
HP:0040092	Asymmetry of the shape of the ears
HP:0040093	Asymmetry of the position of the ears
HP:0040095	Neoplasm of the outer ear
HP:0040096	Neoplasm of the inner ear
HP:0040097	Neoplasm of the ceruminal gland
HP:0040098	Basalioma of the outer ear
HP:0040099	Abnormality of the round window
HP:0040100	Abnormality of the vestibular window
HP:0040101	Cutaneous atresia of the external auditory canal
HP:0040102	Osseous atresia of the external auditory canal
HP:0040103	Cutaneous stenosis of the external auditory canal
HP:0040104	Osseous stenosis of the external auditory canal
HP:0040106	Morphological abnormality of the lateral semicircular canal
HP:0040107	Morphological abnormality of the posterior semicircular canal
HP:0040108	Morphological abnormality of the anterior semicircular canal
HP:0040109	Morphological abnormality of the utricle
HP:0040110	Morphological abnormality of the saccule
HP:0040111	Bilateral external ear deformity
HP:0040112	Abnormal number of tubercles
HP:0040113	Old-aged sensorineural hearing impairment
HP:0040114	Absence of the reflex of the tensor tympani muscle
HP:0040115	Abnormality of the Eustachian tube
HP:0040116	Aplasia of the Eustachian tube
HP:0040117	Atresia of the Eustachian tube
HP:0040118	Stenosis of the Eustachian tube
HP:0040119	Unilateral conductive hearing impairment
HP:0040120	Abnormality of the reflex of the tensor tympanii muscle
HP:0040121	Abnormality of the acoustic reflex
HP:0040122	Impairment of the the acoustic reflex
HP:0040123	Impairment of the reflex of the tensor tympanii muscle
HP:0040124	Patent tuba eustachii
HP:0040126	Abnormal vitamin B12 level
HP:0040127	Abnormal sweat homeostasis
HP:0040128	Abnormal sweat electrolytes
HP:0040129	Abnormal nerve conduction velocity
HP:0040130	Abnormal serum iron
HP:0040131	Abnormal motor nerve conduction velocity
HP:0040132	Abnormal sensory nerve conduction velocity
HP:0040133	Abnormal serum ferritin
HP:0040134	Abnormal hepatic iron concentration
HP:0040135	Abnormal transferrin saturation
HP:0040137	Comedonal acne
HP:0040138	Mucinous histiocytosis
HP:0040139	Lipogranulomatosis
HP:0040140	Degeneration of the striatum
HP:0040141	Tardive dyskinesia
HP:0040142	5-oxoprolinase deficiency
HP:0040143	Dystopic os odontoideum
HP:0040144	L-2-hydroxyglutaric aciduria
HP:0040145	Dicarboxylic acidemia
HP:0040146	D-2-hydroxyglutaric acidemia
HP:0040147	L-2-hydroxyglutaric acidemia
HP:0040148	Cortical myoclonus
HP:0040149	Woolly scalp hair
HP:0040150	Epiblepharon of upper lid
HP:0040151	Epiblepharon of lower lid
HP:0040154	Acne inversa
HP:0040155	Elevated urinary 3-hydroxybutyric acid
HP:0040156	Elevated urinary carboxylic acid
HP:0040157	Abnormal intermamillary distance
HP:0040158	Short intermamillary distance
HP:0040159	Abnormal spaced incisors
HP:0040160	Generalized osteoporosis
HP:0040161	Localized osteoporosis
HP:0040162	Orthokeratosis
HP:0040163	Abnormal pelvis bone morphology
HP:0040164	Lipomas of eyelids
HP:0040165	Periostitis
HP:0040166	Abnormality of the periosteum
HP:0040167	Facial papilloma
HP:0040168	Focal seizures, afebril
HP:0040169	Loose anagen hair
HP:0040170	Abnormality of hair growth
HP:0040171	Decreased serum testosterone level
HP:0040172	Abnormality of occipitofrontalis muscle
HP:0040173	Abnormality of the tongue muscle
HP:0040174	Abnormality of extrinsic muscle of tongue
HP:0040175	Platelet-activating factor acetylhydrolase deficiency
HP:0040176	Abnormal level of phospholipids
HP:0040177	Abnormal level of platelet-activating factor
HP:0040178	Increased level of platelet-activating factor
HP:0040179	Decreased level of platelet-activating factor
HP:0040180	Hyperkeratosis pilaris
HP:0040181	Chapped lip
HP:0040182	Inappropriate sinus tachycardia
HP:0040183	Encopresis
HP:0040184	Oral bleeding
HP:0040185	Macrothrombocytopenia
HP:0040186	Maculopapular exanthema
HP:0040187	Neonatal sepsis
HP:0040188	Osteochondrosis
HP:0040189	Scaling skin
HP:0040190	White scaling skin
HP:0040191	Rectus femoris muscle atrophy
HP:0040192	APUdoma
HP:0040193	obsolete Pinealoblastoma
HP:0040194	Increased head circumference
HP:0040195	Decreased head circumference
HP:0040196	Mild microcephaly
HP:0040197	Encephalomalacia
HP:0040198	Non-medullary thyroid carcinoma
HP:0040199	obsolete Flat midface
HP:0040200	Motor impersistence
HP:0040201	Simultanapraxia
HP:0040202	Abnormal consumption behavior
HP:0040203	Abnormal CSF neopterin level
HP:0040204	Elevated CSF neopterin level
HP:0040205	Decreased CSF neopterin level
HP:0040206	Abnormal level of neopterin
HP:0040207	Abnormal CSF biopterin level
HP:0040208	Elevated CSF biopterin level
HP:0040209	Decreased CSF biopterin level
HP:0040210	Abnormal level of biopterin
HP:0040211	Abnormality of the skin of the palm
HP:0040212	Risus sardonicus
HP:0040213	Hypopnea
HP:0040214	Abnormal insulin level
HP:0040215	Abnormal circulating insulin level
HP:0040216	Hypoinsulinemia
HP:0040217	Elevated hemoglobin A1c
HP:0040218	Reduced natural killer cell count
HP:0040219	Absent natural killer cells
HP:0040220	Abnormal size the dental root
HP:0040221	Hypoplasia of the dental root
HP:0040222	Maternal thrombophilia
HP:0040223	Pulmonary hemorrhage
HP:0040224	Abnormality of fibrinolysis
HP:0040225	Decrease in high molecular weight von Willebrand factor Multimers
HP:0040226	Decreased level of heparin co-factor II
HP:0040227	Decreased level of histidine-rich glycoprotein
HP:0040228	Decreased level of plasminogen
HP:0040229	Decreased level of thrombomodulin
HP:0040230	Decreased level of tissue plasminogen activator
HP:0040231	Abnormal onset of bleeding
HP:0040232	Delayed onset bleeding
HP:0040233	Factor XIII subunit A deficiency
HP:0040234	Factor XIII subunit B deficiency
HP:0040235	Leukocyte inclusion bodies
HP:0040236	Hyperfibrinolysis
HP:0040237	Impaired binding of factor VIII to VWF
HP:0040238	Impaired neutrophil chemotaxis
HP:0040239	Increased plasma vitamin K epoxide after vitamin K supplementation
HP:0040240	Increased ratio of VWF propeptide to VWF antigen
HP:0040241	Increased RIPA
HP:0040242	Muscle haemorrhage
HP:0040243	Prolonged euglobulin clot lysis time
HP:0040244	Prolonged Russell's viper venom time
HP:0040245	Reduced alpha-2-antiplasmin activity
HP:0040246	Reduced antithrombin antigen
HP:0040247	Reduced euglobulin clot lysis time
HP:0040248	Reduced plasminogen activator inhibitor 1 activity
HP:0040249	Reduced plasminogen activator inhibitor 1 antigen
HP:0040250	Reduced prothrombin antigen
HP:0040251	Hand dimples
HP:0040252	Abnormal size of the clitoris
HP:0040253	Increased size of the clitoris
HP:0040254	Decreased size of the clitoris
HP:0040255	Aplasia/Hypoplasia of the clitoris
HP:0040256	Aplastic/Hypoplastic nasopharyngeal adenoids
HP:0040257	Abnormal size of nasopharyngeal adenoids
HP:0040258	Hypoplastic nasopharyngeal adenoids
HP:0040259	Aplastic nasopharyngeal adenoids
HP:0040260	Decreased size of nasopharyngeal adenoids
HP:0040261	Increased size of nasopharyngeal adenoids
HP:0040262	Glue ear
HP:0040263	Jaw ankylosis
HP:0040264	Jaw pain
HP:0040265	Upper limb muscle hypertrophy
HP:0040266	Proximal upper limb muscle hypertrophy
HP:0040267	Distal upper limb muscle hypertrophy
HP:0040268	Recurrent infections of the middle ear
HP:0040269	Blocked Eustachian tube
HP:0040270	Decreased glucose tolerance
HP:0040272	Hyperintensity of MRI T2 signal of the spinal cord
HP:0040273	Adenocarcinoma of the intestines
HP:0040274	Adenocarcinoma of the small intestine
HP:0040275	Adenocarcinoma of the large intestine
HP:0040276	Adenocarcinoma of the colon
HP:0040277	Neoplasm of the pituitary gland
HP:0040278	Prolactinoma
HP:0040279	Frequency
HP:0040280	Obligate
HP:0040281	Very frequent
HP:0040282	Frequent
HP:0040283	Occasional
HP:0040284	Very rare
HP:0040285	Excluded
HP:0040286	Abnormality of axial muscles
HP:0040287	Axial muscle atrophy
HP:0040288	Nasogastric tube feeding
HP:0040289	Cyclic neutropenia
HP:0040290	Abnormality of skeletal muscles
HP:0040291	Skeletal muscle steatosis
HP:0040292	Left hemiplegia
HP:0040293	Right hemiplegia
HP:0040294	Duplicated tongue
HP:0040295	Duplication of the upper lip
HP:0040296	Abnormal location of the eyebrow
HP:0040297	Preauricular cyst
HP:0040298	Hyperplasia of the endometrium
HP:0040299	Decreased circulating free fatty acid level
HP:0040300	Abnormal circulating free fatty acid level
HP:0040301	Increased urinary glycerol
HP:0040302	Hyperglycerolemia
HP:0040303	Decreased serum iron
HP:0040304	Duplication of the sella turcica
HP:0040305	Increased male libido
HP:0040306	Decreased male libido
HP:0040307	Male sexual dysfunction
HP:0040308	Male anorgasmia
HP:0040309	Increased size of the mandible
HP:0040310	Sterile arthritis
HP:0040311	Symetrical distal arthritis
HP:0040312	Temporomandibular arthritis
HP:0040313	Oligoarthritis
HP:0040314	Blind vagina
HP:0040315	Tongue edema
HP:0040316	obsolete Aplasia of the penis
HP:0040317	Blue urine
HP:0040318	Red urine
HP:0040319	Dark urine
HP:0040320	Red-brown urine
HP:0040321	Dark yellow urine
HP:0040322	Purple urine
HP:0040323	Erythema of the eyelids
HP:0040324	Heliotrope rash
HP:0040325	Bull's eye rash
HP:0040326	Hypoplasia of the olfactory bulb
HP:0040327	Abnormal morphology of the olfactory bulb
HP:0040328	Focal hyperintensity of cerebral white matter on MRI
HP:0040329	Multifocal hyperintensity of cerebral white matter on MRI
HP:0040330	Confluent hyperintensity of cerebral white matter on MRI
HP:0040331	Focal hypointensity of cerebral white matter on MRI
HP:0040332	Multifocal hypointensity of cerebral white matter on MRI
HP:0040333	Confluent hypointensity of cerebral white matter on MRI
HP:0040334	Purulent rhinitis
HP:0045001	Abnormal ossification of the trapezium
HP:0045002	Absent ossification of the trapezium
HP:0045003	Abnormal ossification of the scaphoid
HP:0045004	Abnormal ossification of the trapezoid bone
HP:0045005	Neural tube defect
HP:0045006	Aplasia of lymphatic vessels
HP:0045007	Abnormality of the substantia nigra
HP:0045008	Abnormal shape of the radius
HP:0045009	Abnormal morphology of the radius
HP:0045010	Abnormality of peripheral nerves
HP:0045011	Decreased urine bicarbonate concentration
HP:0045012	Decreased urinary catecholamine concentration
HP:0045013	obsolete Decreased urinary glucose concentration
HP:0045014	Hypolipidemia
HP:0045016	Elevated serum long-chain fatty acids
HP:0045017	Congenital malformation of the left heart
HP:0045018	Partial duplication of eyebrows
HP:0045025	Narrow palpebral fissure
HP:0045026	Abnormality of the mediastinum
HP:0045027	Abnormality of the thoracic cavity
HP:0045028	Type III lissencephaly
HP:0045029	Eosinophilic fasciitis
HP:0045034	Elevated urinary aminoisobutyric acid
HP:0045035	Decreased urinary copper concentration
HP:0045036	Abnormal urinary copper concentration
HP:0045037	Abnormality of jaw muscles
HP:0045038	Gastric lymphoma
HP:0045039	Osteolysis involving bones of the upper limbs
HP:0045040	Abnormal lactate dehydrogenase activity
HP:0045041	Reduced lactate dehydrogenase B level
HP:0045042	Decreased serum complement C4
HP:0045043	Decreased serum complement C4a
HP:0045044	Decreased serum complement C4b
HP:0045045	Elevated plasma acylcarnitine levels
HP:0045046	Reduced insulin like growth factor binding protein acid labile subunit level
HP:0045047	HbS hemoglobin
HP:0045048	Increased HbA2 hemoglobin
HP:0045049	Abnormal DLCO
HP:0045050	Increased DLCO
HP:0045051	Decreased DLCO
HP:0045052	Abnormality of the brachial nerve plexus
HP:0045053	Abnormality of the lumbosacral nerve plexus
HP:0045054	Brachial plexus neuropathy
HP:0045055	Tiger tail banding
HP:0045056	Abnormal levels of alpha-fetoprotein
HP:0045057	Decreased levels of alpha-fetoprotein
HP:0045058	Abnormality of the testis size
HP:0045059	Hyperkeratotic papule
HP:0045060	Aplasia/hypoplasia involving bones of the extremities
HP:0045061	Decreased carnitine level in liver
HP:0045063	Increased PIVKA-II
HP:0045073	Serositis
HP:0045074	Thin eyebrow
HP:0045075	Sparse eyebrow
HP:0045079	Distal femoral metaphyseal irregularity
HP:0045080	Decreased proportion of CD3-positive T cells
HP:0045081	Abnormality of body mass index
HP:0045082	Decreased body mass index
HP:0045083	obsolete Increased body mass index
HP:0045084	Limb myoclonus
HP:0045085	Atrophy of masseter muscle
HP:0045086	Knee joint hypermobility
HP:0045087	Hip joint hypermobility
HP:0100000	Early onset of sexual maturation
HP:0100001	Malignant mesothelioma
HP:0100002	Pleural mesothelioma
HP:0100003	Peritoneal mesothelioma
HP:0100004	Pericardial mesothelioma
HP:0100005	Testicular mesothelioma
HP:0100006	Neoplasm of the central nervous system
HP:0100007	Neoplasm of the peripheral nervous system
HP:0100008	Schwannoma
HP:0100009	Intracranial meningioma
HP:0100010	Spinal meningioma
HP:0100011	Scleral schwannoma
HP:0100012	Neoplasm of the eye
HP:0100013	Neoplasm of the breast
HP:0100014	Epiretinal membrane
HP:0100015	Stahl ear
HP:0100016	Abnormality of mesentery morphology
HP:0100017	Capsular cataract
HP:0100018	Nuclear cataract
HP:0100019	Cortical cataract
HP:0100020	Posterior capsular cataract
HP:0100021	Cerebral palsy
HP:0100022	Abnormality of movement
HP:0100023	Recurrent hand flapping
HP:0100024	Conspicuously happy disposition
HP:0100025	Overfriendliness
HP:0100026	Arteriovenous malformation
HP:0100027	Recurrent pancreatitis
HP:0100028	Ectopic thyroid
HP:0100029	Lingual thyroid
HP:0100030	Accessory ectopic thyroid tissue
HP:0100031	Neoplasm of the thyroid gland
HP:0100033	Tics
HP:0100034	Motor tics
HP:0100035	Phonic tics
HP:0100036	Pseudo-fractures
HP:0100037	Abnormality of the scalp hair
HP:0100038	Slow-growing scalp hair
HP:0100039	Thickened cortex of bones
HP:0100040	Broad 2nd toe
HP:0100041	Broad 3rd toe
HP:0100042	Broad 4th toe
HP:0100043	Broad 5th toe
HP:0100044	Absent epiphyses of the 2nd toe
HP:0100045	Bracket epiphyses of the 2nd toe
HP:0100046	Cone-shaped epiphyses of the 2nd toe
HP:0100047	Enlarged epiphyses of the 2nd toe
HP:0100048	Fragmentation of the epiphyses of the 2nd toe
HP:0100049	Irregular epiphyses of the 2nd toe
HP:0100050	Ivory epiphyses of the 2nd toe
HP:0100051	Pseudoepiphyses of the 2nd toe
HP:0100052	Small epiphyses of the 2nd toe
HP:0100053	Stippling of the epiphyses of the 2nd toe
HP:0100054	Triangular epiphyses of the 2nd toe
HP:0100055	Absent epiphyses of the 3rd toe
HP:0100056	Bracket epiphyses of the 3rd toe
HP:0100057	Cone-shaped epiphyses of the 3rd toe
HP:0100058	Enlarged epiphyses of the 3rd toe
HP:0100059	Fragmentation of the epiphyses of the 3rd toe
HP:0100060	Irregular epiphyses of the 3rd toe
HP:0100061	Ivory epiphyses of the 3rd toe
HP:0100062	Pseudoepiphyses of the 3rd toe
HP:0100063	Small epiphyses of the 3rd toe
HP:0100064	Stippling of the epiphyses of the 3rd toe
HP:0100065	Triangular epiphyses of the 3rd toe
HP:0100066	Absent epiphyses of the 4th toe
HP:0100067	Bracket epiphyses of the 4th toe
HP:0100068	Cone-shaped epiphyses of the 4th toe
HP:0100069	Enlarged epiphyses of the 4th toe
HP:0100070	Fragmentation of the epiphyses of the 4th toe
HP:0100071	Irregular epiphyses of the 4th toe
HP:0100072	Ivory epiphyses of the 4th toe
HP:0100073	Pseudoepiphyses of the 4th toe
HP:0100074	Small epiphyses of the 4th toe
HP:0100075	Stippling of the epiphyses of the 4th toe
HP:0100076	Triangular epiphyses of the 4th toe
HP:0100077	Absent epiphyses of the 5th toe
HP:0100078	Bracket epiphyses of the 5th toe
HP:0100079	Cone-shaped epiphyses of the 5th toe
HP:0100080	Enlarged epiphyses of the 5th toe
HP:0100081	Fragmentation of the epiphyses of the 5th toe
HP:0100082	Irregular epiphyses of the 5th toe
HP:0100083	Ivory epiphyses of the 5th toe
HP:0100084	Pseudoepiphyses of the 5th toe
HP:0100085	Small epiphyses of the 5th toe
HP:0100086	Stippling of the epiphyses of the 5th toe
HP:0100087	Triangular epiphyses of the 5th toe
HP:0100088	Abnormality of the epiphysis of the distal phalanx of the 2nd toe
HP:0100089	Abnormality of the epiphysis of the middle phalanx of the 2nd toe
HP:0100090	Abnormality of the epiphysis of the proximal phalanx of the 2nd toe
HP:0100091	Abnormality of the epiphysis of the distal phalanx of the 3rd toe
HP:0100092	Abnormality of the epiphysis of the middle phalanx of the 3rd toe
HP:0100093	Abnormality of the epiphysis of the proximal phalanx of the 3rd toe
HP:0100094	Abnormality of the epiphysis of the distal phalanx of the 4th toe
HP:0100095	Abnormality of the epiphysis of the middle phalanx of the 4th toe
HP:0100096	Abnormality of the epiphysis of the proximal phalanx of the 4th toe
HP:0100097	Abnormality of the epiphysis of the distal phalanx of the 5th toe
HP:0100098	Abnormality of the epiphysis of the middle phalanx of the 5th toe
HP:0100099	Abnormality of the epiphysis of the proximal phalanx of the 5th toe
HP:0100100	Absent epiphysis of the distal phalanx of the 2nd toe
HP:0100101	Bracket epiphysis of the distal phalanx of the 2nd toe
HP:0100102	Cone-shaped epiphysis of the distal phalanx of the 2nd toe
HP:0100103	Enlarged epiphysis of the distal phalanx of the 2nd toe
HP:0100104	Fragmentation of the epiphysis of the distal phalanx of the 2nd toe
HP:0100105	Irregular epiphysis of the distal phalanx of the 2nd toe
HP:0100106	Ivory epiphysis of the distal phalanx of the 2nd toe
HP:0100107	Pseudoepiphysis of the distal phalanx of the 2nd toe
HP:0100108	Small epiphysis of the distal phalanx of the 2nd toe
HP:0100109	Stippling of the epiphysis of the distal phalanx of the 2nd toe
HP:0100110	Triangular epiphysis of the distal phalanx of the 2nd toe
HP:0100111	Absent epiphysis of the middle phalanx of the 2nd toe
HP:0100112	Bracket epiphysis of the middle phalanx of the 2nd toe
HP:0100113	Cone-shaped epiphysis of the middle phalanx of the 2nd toe
HP:0100114	Enlarged epiphysis of the middle phalanx of the 2nd toe
HP:0100115	Fragmentation of the epiphysis of the middle phalanx of the 2nd toe
HP:0100116	Irregular epiphysis of the middle phalanx of the 2nd toe
HP:0100117	Ivory epiphysis of the middle phalanx of the 2nd toe
HP:0100118	Pseudoepiphysis of the middle phalanx of the 2nd toe
HP:0100119	Small epiphysis of the middle phalanx of the 2nd toe
HP:0100120	Stippling of the epiphysis of the middle phalanx of the 2nd toe
HP:0100121	Triangular epiphysis of the middle phalanx of the 2nd toe
HP:0100122	Absent epiphysis of the proximal phalanx of the 2nd toe
HP:0100123	Bracket epiphysis of the proximal phalanx of the 2nd toe
HP:0100124	Cone-shaped epiphysis of the proximal phalanx of the 2nd toe
HP:0100125	Enlarged epiphysis of the proximal phalanx of the 2nd toe
HP:0100126	Fragmentation of the epiphysis of the proximal phalanx of the 2nd toe
HP:0100127	Irregular epiphysis of the proximal phalanx of the 2nd toe
HP:0100128	Ivory epiphysis of the proximal phalanx of the 2nd toe
HP:0100129	Pseudoepiphysis of the proximal phalanx of the 2nd toe
HP:0100130	Small epiphysis of the proximal phalanx of the 2nd toe
HP:0100131	Stippling of the epiphysis of the proximal phalanx of the 2nd toe
HP:0100132	Triangular epiphysis of the proximal phalanx of the 2nd toe
HP:0100133	Abnormality of the pubic hair
HP:0100134	Abnormality of the axillary hair
HP:0100135	Absent epiphysis of the distal phalanx of the 3rd toe
HP:0100136	Bracket epiphysis of the distal phalanx of the 3rd toe
HP:0100137	Cone-shaped epiphysis of the distal phalanx of the 3rd toe
HP:0100138	Enlarged epiphysis of the distal phalanx of the 3rd toe
HP:0100139	Fragmentation of the epiphysis of the distal phalanx of the 3rd toe
HP:0100140	Irregular epiphysis of the distal phalanx of the 3rd toe
HP:0100141	Ivory epiphysis of the distal phalanx of the 3rd toe
HP:0100142	Pseudoepiphysis of the distal phalanx of the 3rd toe
HP:0100143	Small epiphysis of the distal phalanx of the 3rd toe
HP:0100144	Stippling of the epiphysis of the distal phalanx of the 3rd toe
HP:0100145	Triangular epiphysis of the distal phalanx of the 3rd toe
HP:0100146	Absent epiphysis of the middle phalanx of the 3rd toe
HP:0100147	Bracket epiphysis of the middle phalanx of the 3rd toe
HP:0100148	Cone-shaped epiphysis of the middle phalanx of the 3rd toe
HP:0100149	Enlarged epiphysis of the middle phalanx of the 3rd toe
HP:0100150	Fragmentation of the epiphysis of the middle phalanx of the 3rd toe
HP:0100151	Irregular epiphysis of the middle phalanx of the 3rd toe
HP:0100152	Ivory epiphysis of the middle phalanx of the 3rd toe
HP:0100153	Pseudoepiphysis of the middle phalanx of the 3rd toe
HP:0100154	Small epiphysis of the middle phalanx of the 3rd toe
HP:0100155	Stippling of the epiphysis of the middle phalanx of the 3rd toe
HP:0100156	Triangular epiphysis of the middle phalanx of the 3rd toe
HP:0100157	Absent epiphysis of the proximal phalanx of the 3rd toe
HP:0100158	Bracket epiphysis of the proximal phalanx of the 3rd toe
HP:0100159	Cone-shaped epiphysis of the proximal phalanx of the 3rd toe
HP:0100160	Enlarged epiphysis of the proximal phalanx of the 3rd toe
HP:0100161	Fragmentation of the epiphysis of the proximal phalanx of the 3rd toe
HP:0100162	Irregular epiphysis of the proximal phalanx of the 3rd toe
HP:0100163	Ivory epiphysis of the proximal phalanx of the 3rd toe
HP:0100164	Pseudoepiphysis of the proximal phalanx of the 3rd toe
HP:0100165	Small epiphysis of the proximal phalanx of the 3rd toe
HP:0100166	Stippling of the epiphysis of the proximal phalanx of the 3rd toe
HP:0100167	Triangular epiphysis of the proximal phalanx of the 3rd toe
HP:0100168	Fragmented epiphyses
HP:0100169	Absent epiphysis of the distal phalanx of the 4th toe
HP:0100170	Bracket epiphysis of the distal phalanx of the 4th toe
HP:0100171	Cone-shaped epiphysis of the distal phalanx of the 4th toe
HP:0100172	Enlarged epiphysis of the distal phalanx of the 4th toe
HP:0100173	Fragmentation of the epiphysis of the distal phalanx of the 4th toe
HP:0100174	Irregular epiphysis of the distal phalanx of the 4th toe
HP:0100175	Ivory epiphysis of the distal phalanx of the 4th toe
HP:0100176	Pseudoepiphysis of the distal phalanx of the 4th toe
HP:0100177	Small epiphysis of the distal phalanx of the 4th toe
HP:0100178	Stippling of the epiphysis of the distal phalanx of the 4th toe
HP:0100179	Triangular epiphysis of the distal phalanx of the 4th toe
HP:0100180	Absent epiphysis of the middle phalanx of the 4th toe
HP:0100181	Bracket epiphysis of the middle phalanx of the 4th toe
HP:0100182	Cone-shaped epiphysis of the middle phalanx of the 4th toe
HP:0100183	Enlarged epiphysis of the middle phalanx of the 4th toe
HP:0100184	Fragmentation of the epiphysis of the middle phalanx of the 4th toe
HP:0100185	Irregular epiphysis of the middle phalanx of the 4th toe
HP:0100186	Ivory epiphysis of the middle phalanx of the 4th toe
HP:0100187	Pseudoepiphysis of the middle phalanx of the 4th toe
HP:0100188	Small epiphysis of the middle phalanx of the 4th toe
HP:0100189	Stippling of the epiphysis of the middle phalanx of the 4th toe
HP:0100190	Triangular epiphysis of the middle phalanx of the 4th toe
HP:0100191	Absent epiphysis of the proximal phalanx of the 4th toe
HP:0100192	Bracket epiphysis of the proximal phalanx of the 4th toe
HP:0100193	Cone-shaped epiphysis of the proximal phalanx of the 4th toe
HP:0100194	Enlarged epiphysis of the proximal phalanx of the 4th toe
HP:0100195	Fragmentation of the epiphysis of the proximal phalanx of the 4th toe
HP:0100196	Irregular epiphysis of the proximal phalanx of the 4th toe
HP:0100197	Ivory epiphysis of the proximal phalanx of the 4th toe
HP:0100198	Pseudoepiphysis of the proximal phalanx of the 4th toe
HP:0100199	Small epiphysis of the proximal phalanx of the 4th toe
HP:0100200	Stippling of the epiphysis of the proximal phalanx of the 4th toe
HP:0100201	Triangular epiphysis of the proximal phalanx of the 4th toe
HP:0100202	Absent epiphysis of the distal phalanx of the 5th toe
HP:0100203	Bracket epiphysis of the distal phalanx of the 5th toe
HP:0100204	Cone-shaped epiphysis of the distal phalanx of the 5th toe
HP:0100205	Enlarged epiphysis of the distal phalanx of the 5th toe
HP:0100206	Fragmentation of the epiphysis of the distal phalanx of the 5th toe
HP:0100207	Irregular epiphysis of the distal phalanx of the 5th toe
HP:0100208	Ivory epiphysis of the distal phalanx of the 5th toe
HP:0100209	Pseudoepiphysis of the distal phalanx of the 5th toe
HP:0100210	Small epiphysis of the distal phalanx of the 5th toe
HP:0100211	Stippling of the epiphysis of the distal phalanx of the 5th toe
HP:0100212	Triangular epiphysis of the distal phalanx of the 5th toe
HP:0100213	Absent epiphysis of the middle phalanx of the 5th toe
HP:0100214	Bracket epiphysis of the middle phalanx of the 5th toe
HP:0100215	Cone-shaped epiphysis of the middle phalanx of the 5th toe
HP:0100216	Enlarged epiphysis of the middle phalanx of the 5th toe
HP:0100217	Fragmentation of the epiphysis of the middle phalanx of the 5th toe
HP:0100218	Irregular epiphysis of the middle phalanx of the 5th toe
HP:0100219	Ivory epiphysis of the middle phalanx of the 5th toe
HP:0100220	Pseudoepiphysis of the middle phalanx of the 5th toe
HP:0100221	Small epiphysis of the middle phalanx of the 5th toe
HP:0100222	Stippling of the epiphysis of the middle phalanx of the 5th toe
HP:0100223	Triangular epiphysis of the middle phalanx of the 5th toe
HP:0100224	Absent epiphysis of the proximal phalanx of the 5th toe
HP:0100225	Bracket epiphysis of the proximal phalanx of the 5th toe
HP:0100226	Cone-shaped epiphysis of the proximal phalanx of the 5th toe
HP:0100227	Enlarged epiphysis of the proximal phalanx of the 5th toe
HP:0100228	Fragmentation of the epiphysis of the proximal phalanx of the 5th toe
HP:0100229	Irregular epiphysis of the proximal phalanx of the 5th toe
HP:0100230	Ivory epiphysis of the proximal phalanx of the 5th toe
HP:0100231	Pseudoepiphysis of the proximal phalanx of the 5th toe
HP:0100232	Small epiphysis of the proximal phalanx of the 5th toe
HP:0100233	Stippling of the epiphysis of the proximal phalanx of the 5th toe
HP:0100234	Triangular epiphysis of the proximal phalanx of the 5th toe
HP:0100235	Synostosis involving bones of the toes
HP:0100237	Proximal foot symphalangism
HP:0100238	Synostosis involving bones of the upper limbs
HP:0100240	Synostosis of joints
HP:0100241	Ectopic respiratory mucosa
HP:0100242	Sarcoma
HP:0100243	Leiomyosarcoma
HP:0100244	Fibrosarcoma
HP:0100245	Desmoid tumors
HP:0100246	Osteoma
HP:0100247	Recurrent singultus
HP:0100248	Hemiballismus
HP:0100249	Calcification of muscles
HP:0100250	Meningeal calcification
HP:0100251	Lipomas of the central neryous system
HP:0100252	Diaphyseal dysplasia
HP:0100253	Abnormality of the medullary cavity of the long bones
HP:0100254	Stenosis of the medullary cavity of the long bones
HP:0100255	Metaphyseal dysplasia
HP:0100256	Senile plaques
HP:0100257	Ectrodactyly
HP:0100258	Preaxial polydactyly
HP:0100259	Postaxial polydactyly
HP:0100260	Mesoaxial polydactyly
HP:0100261	Abnormal tendon morphology
HP:0100262	Synostosis involving digits
HP:0100263	Distal symphalangism
HP:0100264	Proximal symphalangism
HP:0100265	Synostosis of metacarpals/metatarsals
HP:0100266	Synostosis of carpals/tarsals
HP:0100267	Lip pit
HP:0100268	Upper lip pit
HP:0100269	Paramedian lip pit
HP:0100270	Abnormality of dorsoventral patterning of the limbs
HP:0100271	Hyponasal speech
HP:0100272	Branchial sinus
HP:0100273	Neoplasm of the colon
HP:0100274	Gustatory lacrimation
HP:0100275	Diffuse cerebellar atrophy
HP:0100276	Skin pit
HP:0100277	Periauricular skin pits
HP:0100279	Ulcerative colitis
HP:0100280	Crohn's disease
HP:0100281	Chronic colitis
HP:0100282	Acute colitis
HP:0100283	EMG: continuous motor unit activity at rest
HP:0100284	EMG: myotonic discharges
HP:0100285	EMG: impaired neuromuscular transmission
HP:0100287	EMG: slow motor conduction
HP:0100288	EMG: myokymic discharges
HP:0100289	Abnormality of pattern reversal visual evoked potentials
HP:0100290	Abnormality of peripheral somatosensory evoked potentials
HP:0100291	Abnormality of central somatosensory evoked potentials
HP:0100292	Amyloidosis of peripheral nerves
HP:0100293	Muscle fiber hypertrophy
HP:0100295	Muscle fiber atrophy
HP:0100296	Perifascicular muscle fiber atrophy
HP:0100297	Increased endomysial connective tissue
HP:0100298	Motheaten muscle fibers
HP:0100299	Muscle fiber inclusion bodies
HP:0100300	Desmin bodies
HP:0100301	Muscle fiber tubular inclusions
HP:0100302	Muscle fiber tubuloreticular inclusions
HP:0100303	Muscle fiber cytoplasmatic inclusion bodies
HP:0100304	Muscle fiber intranuclear inclusion bodies
HP:0100305	Ring fibers
HP:0100306	Muscle fiber hyaline bodies
HP:0100307	Cerebellar hemisphere hypoplasia
HP:0100308	Cerebral cortical hemiatrophy
HP:0100309	Subdural hemorrhage
HP:0100310	Epidural hemorrhage
HP:0100311	Cerebral ventricular adhesions
HP:0100312	Cerebral germinoma
HP:0100313	Cerebral granulomatosis
HP:0100314	Cerebral inclusion bodies
HP:0100315	Lewy bodies
HP:0100316	Hirano bodies
HP:0100317	Argyrophilic inclusion bodies
HP:0100318	Lafora bodies
HP:0100319	Cerebral hyaline bodies
HP:0100320	Rosenthal fibres
HP:0100321	Abnormality of the dentate nucleus
HP:0100322	Aplasia of the pyramidal tract
HP:0100323	Juvenile aseptic necrosis
HP:0100324	Scleroderma
HP:0100326	Immunologic hypersensitivity
HP:0100327	Cow milk allergy
HP:0100328	Carpometacarpal synostosis
HP:0100329	Tarsometatarsal synostosis
HP:0100333	Unilateral cleft lip
HP:0100334	Unilateral cleft palate
HP:0100335	Non-midline cleft lip
HP:0100336	Bilateral cleft lip
HP:0100337	Bilateral cleft palate
HP:0100338	Non-midline cleft palate
HP:0100339	Abnormality of the os naviculare pedis
HP:0100340	Fibular deviation of the 4th toe
HP:0100341	Tibial deviation of the 4th toe
HP:0100342	Fibular deviation of the 3rd toe
HP:0100343	Tibial deviation of the 3rd toe
HP:0100344	Fibular deviation of the 2nd toe
HP:0100345	Tibial deviation of the 2nd toe
HP:0100346	Fibular deviation of the 5th toe
HP:0100347	Tibial deviation of the 5th toe
HP:0100348	Contracture of the proximal interphalangeal joint of the 2nd toe
HP:0100349	Contracture of the proximal interphalangeal joint of the 3rd toe
HP:0100350	Contracture of the proximal interphalangeal joint of the 4th toe
HP:0100351	Contractures of the proximal interphalangeal joint of the 5th toe
HP:0100352	Contracture of the distal interphalangeal joint of the 2nd toe
HP:0100353	Contracture of the distal interphalangeal joint of the 3rd toe
HP:0100354	Contracture of the distal interphalangeal joint of the 4th toe
HP:0100355	Contractures of the distal interphalangeal joint of the 5th toe
HP:0100356	Contracture of the metatarsophalangeal joint of the 2nd toe
HP:0100357	Contracture of the metatarsophalangeal joint of the 3rd toe
HP:0100358	Contracture of the metatarsophalangeal joint of the 4th toe
HP:0100359	Contracture of the metatarsophalangeal joint of the 5th toe
HP:0100360	Contractures of the joints of the upper limbs
HP:0100362	Aplasia of the phalanges of the 3rd toe
HP:0100363	Aplasia of the phalanges of the 4th toe
HP:0100364	Aplasia of the phalanges of the 5th toe
HP:0100366	Short phalanx of the 3rd toe
HP:0100367	Short phalanx of the 4th toe
HP:0100368	Short phalanx of the 5th toe
HP:0100369	Aplasia/Hypoplasia of the distal phalanx of the 3rd toe
HP:0100370	Aplasia/Hypoplasia of the distal phalanx of the 4th toe
HP:0100371	Aplasia/Hypoplasia of the distal phalanx of the 5th toe
HP:0100372	Aplasia/Hypoplasia of the middle phalanx of the 3rd toe
HP:0100373	Aplasia/Hypoplasia of the middle phalanx of the 4th toe
HP:0100374	Aplasia/Hypoplasia of the middle phalanx of the 5th toe
HP:0100375	Aplasia/hypoplasia of the proximal phalanx of the 3rd toe
HP:0100376	Aplasia/hypoplasia of the proximal phalanx of the 4th toe
HP:0100377	Aplasia/hypoplasia of the proximal phalanx of the 5th toe
HP:0100378	Absent distal phalanx of the 3rd toe
HP:0100379	Aplasia of the distal phalanx of the 4th toe
HP:0100380	Aplasia of the distal phalanx of the 5th toe
HP:0100381	Absent middle phalanx of the 3rd toe
HP:0100382	Aplasia of the middle phalanx of the 4th toe
HP:0100383	Aplasia of the middle phalanx of the 5th toe
HP:0100384	Absent proximal phalanx of the 3rd toe
HP:0100385	Aplasia of the proximal phalanx of the 4th toe
HP:0100386	Aplasia of the proximal phalanx of the 5th toe
HP:0100387	Aplasia of the middle phalanges of the toes
HP:0100388	Aplasia of the proximal phalanges of the toes
HP:0100389	Short distal phalanx of the 3rd toe
HP:0100390	Short distal phalanx of the 4th toe
HP:0100391	Short distal phalanx of the 5th toe
HP:0100392	Short middle phalanx of the 3rd toe
HP:0100393	Short middle phalanx of the 4th toe
HP:0100394	Short middle phalanx of the 5th toe
HP:0100395	Short proximal phalanx of the 3rd toe
HP:0100396	Short proximal phalanx of the 4th toe
HP:0100397	Short proximal phalanx of the 5th toe
HP:0100398	Duplication of the distal phalanx of the 3rd toe
HP:0100399	Duplication of the distal phalanx of the 4th toe
HP:0100400	Duplication of the distal phalanx of the 5th toe
HP:0100401	Duplication of the middle phalanx of the 3rd toe
HP:0100402	Duplication of the middle phalanx of the 4th toe
HP:0100403	Duplication of the middle phalanx of the 5th toe
HP:0100404	Duplication of the proximal phalanx of the 3rd toe
HP:0100405	Duplication of the proximal phalanx of the 4th toe
HP:0100406	Duplication of the proximal phalanx of the 5th toe
HP:0100407	Complete duplication of the distal phalanx of the 3rd toe
HP:0100408	Complete duplication of the distal phalanx of the 4th toe
HP:0100409	Complete duplication of the distal phalanx of the 5th toe
HP:0100410	Complete duplication of the middle phalanx of the 3rd toe
HP:0100411	Complete duplication of the middle phalanx of the 4th toe
HP:0100412	Complete duplication of the middle phalanx of the 5th toe
HP:0100413	Complete duplication of the proximal phalanx of the 3rd toe
HP:0100414	Complete duplication of the proximal phalanx of the 4th toe
HP:0100415	Complete duplication of the proximal phalanx of the 5th toe
HP:0100416	Partial duplication of the distal phalanx of the 3rd toe
HP:0100417	Partial duplication of the distal phalanx of the 4th toe
HP:0100418	Partial duplication of the distal phalanx of the 5th toe
HP:0100419	Partial duplication of the middle phalanx of the 3rd toe
HP:0100420	Partial duplication of the middle phalanx of the 4th toe
HP:0100421	Partial duplication of the middle phalanx of the 5th toe
HP:0100422	Partial duplication of the proximal phalanx of the 3rd toe
HP:0100423	Partial duplication of the proximal phalanx of the 4th toe
HP:0100424	Partial duplication of the proximal phalanx of the 5th toe
HP:0100425	Broad middle phalanx of the 3rd toe
HP:0100426	Broad middle phalanx of the 4th toe
HP:0100427	Broad middle phalanx of the 5th toe
HP:0100428	Broad proximal phalanx of the 3rd toe
HP:0100429	Broad proximal phalanx of the 4th toe
HP:0100430	Broad proximal phalanx of the 5th toe
HP:0100431	Broad distal phalanx of the 3rd toe
HP:0100432	Broad distal phalanx of the 4th toe
HP:0100433	Broad distal phalanx of the 5th toe
HP:0100434	Bullet-shaped middle phalanx of the 3rd toe
HP:0100435	Bullet-shaped middle phalanx of the 4th toe
HP:0100436	Bullet-shaped middle phalanx of the 5th toe
HP:0100437	Bullet-shaped proximal phalanx of the 3rd toe
HP:0100438	Bullet-shaped proximal phalanx of the 4th toe
HP:0100439	Bullet-shaped proximal phalanx of the 5th toe
HP:0100440	Bullet-shaped distal phalanx of the 3rd toe
HP:0100441	Bullet-shaped distal phalanx of the 4th toe
HP:0100442	Bullet-shaped distal phalanx of the 5th toe
HP:0100443	Curved middle phalanx of the 3rd toe
HP:0100444	Curved middle phalanx of the 4th toe
HP:0100445	Curved middle phalanx of the 5th toe
HP:0100446	Curved proximal phalanx of the 3rd toe
HP:0100447	Curved proximal phalanx of the 4th toe
HP:0100448	Curved proximal phalanx of the 5th toe
HP:0100449	Curved distal phalanx of the 3rd toe
HP:0100450	Curved distal phalanx of the 4th toe
HP:0100451	Curved distal phalanx of the 5th toe
HP:0100452	Osteolytic defects of the middle phalanx of the 3rd toe
HP:0100453	Osteolytic defects of the middle phalanx of the 4th toe
HP:0100454	Osteolytic defects of the middle phalanx of the 5th toe
HP:0100455	Osteolytic defects of the proximal phalanx of the 3rd toe
HP:0100456	Osteolytic defects of the proximal phalanx of the 4th toe
HP:0100457	Osteolytic defects of the proximal phalanx of the 5th toe
HP:0100458	Osteolytic defects of the distal phalanx of the 3rd toe
HP:0100459	Osteolytic defects of the distal phalanx of the 4th toe
HP:0100460	Osteolytic defects of the distal phalanx of the 5th toe
HP:0100461	Patchy sclerosis of the middle phalanx of the 3rd toe
HP:0100462	Patchy sclerosis of the middle phalanx of the 4th toe
HP:0100463	Patchy sclerosis of the middle phalanx of the 5th toe
HP:0100464	Patchy sclerosis of the proximal phalanx of the 3rd toe
HP:0100465	Patchy sclerosis of the proximal phalanx of the 4th toe
HP:0100466	Patchy sclerosis of the proximal phalanx of the 5th toe
HP:0100467	Patchy sclerosis of the distal phalanx of the 3rd toe
HP:0100468	Patchy sclerosis of the distal phalanx of the 4th toe
HP:0100469	Patchy sclerosis of the distal phalanx of the 5th toe
HP:0100470	Symphalangism affecting the middle phalanx of the 3rd toe
HP:0100471	Symphalangism affecting the middle phalanx of the 4th toe
HP:0100472	Symphalangism affecting the middle phalanx of the 5th toe
HP:0100473	Symphalangism affecting the proximal phalanx of the 3rd toe
HP:0100474	Symphalangism affecting the proximal phalanx of the 4th toe
HP:0100475	Symphalangism affecting the proximal phalanx of the 5th toe
HP:0100476	Symphalangism affecting the distal phalanx of the 3rd toe
HP:0100477	Symphalangism affecting the distal phalanx of the 4th toe
HP:0100478	Symphalangism affecting the distal phalanx of the 5th toe
HP:0100480	Proximal/middle symphalangism of 3rd toe
HP:0100481	Proximal/middle symphalangism of 4th toe
HP:0100482	Proximal/middle symphalangism of 5th toe
HP:0100483	Symphalangism of the proximal phalanx of the 2nd toe with the 2nd metatarsal
HP:0100484	Symphalangism of the proximal phalanx of the 3rd toe with the 3rd metatarsal
HP:0100485	Symphalangism of the proximal phalanx of the 4th toe with the 4th metatarsal
HP:0100486	Symphalangism of the proximal phalanx of the 5th toe with the 5th metatarsal
HP:0100487	Triangular shaped distal phalanx of the 5th toe
HP:0100488	Synostosis of the proximal phalanx of the hallux with the 1st metatarsal
HP:0100489	Proximal/middle symphalangism of 2nd toe
HP:0100490	Camptodactyly of finger
HP:0100491	Abnormality of lower limb joint
HP:0100492	Joint contractures involving the joints of the feet
HP:0100493	Hypoammonemia
HP:0100494	Abnormal mast cell morphology
HP:0100495	Mastocytosis
HP:0100496	Abnormality of the vitamin B3 metabolism
HP:0100497	Vitamin B3 deficiency
HP:0100498	Deviation of toes
HP:0100499	Tibial deviation of toes
HP:0100500	Fibular deviation of toes
HP:0100501	Recurrent bronchiolitis
HP:0100502	Vitamin B12 deficiency
HP:0100503	Vitamin B1 deficiency
HP:0100504	Vitamin B2 deficiency
HP:0100505	Vitamin B5 deficiency
HP:0100506	Vitamin B8 deficiency
HP:0100507	Reduced blood folate concentration
HP:0100508	Abnormality of vitamin metabolism
HP:0100509	Abnormality of vitamin C metabolism
HP:0100510	Vitamin C deficiency
HP:0100511	Abnormality of vitamin D metabolism
HP:0100512	Vitamin D deficiency
HP:0100513	Vitamin E deficiency
HP:0100514	Abnormality of vitamin E metabolism
HP:0100515	Pollakisuria
HP:0100516	Neoplasm of the ureter
HP:0100517	Neoplasm of the urethra
HP:0100518	Dysuria
HP:0100519	Anuria
HP:0100520	Oliguria
HP:0100521	Neoplasm of the thymus
HP:0100522	Thymoma
HP:0100523	Liver abscess
HP:0100524	Limb duplication
HP:0100525	Urachus fistula
HP:0100526	Neoplasm of the lung
HP:0100527	Neoplasia of the pleura
HP:0100528	Pleuropulmonary blastoma
HP:0100529	Abnormality of phosphate homeostasis
HP:0100530	Abnormality of calcium-phosphate metabolism
HP:0100531	Wind-swept deformity of the knees
HP:0100532	Scleritis
HP:0100533	Inflammatory abnormality of the eye
HP:0100534	Episcleritis
HP:0100535	Tibiofibular diastasis
HP:0100536	Abnormality of the fascia
HP:0100537	Fasciitis
HP:0100538	Abnormality of the supraorbital ridges
HP:0100539	Periorbital edema
HP:0100540	Palpebral edema
HP:0100541	Femoral hernia
HP:0100542	Abnormal localization of kidney
HP:0100543	Cognitive impairment
HP:0100544	Neoplasm of the heart
HP:0100545	Arterial stenosis
HP:0100546	Carotid artery stenosis
HP:0100547	Abnormality of forebrain morphology
HP:0100548	Exstrophy
HP:0100550	Tendon rupture
HP:0100551	Neoplasm of the trachea
HP:0100552	Neoplasm of the tracheobronchial system
HP:0100553	Hemihypertrophy of lower limb
HP:0100554	Hemihypertrophy of upper limb
HP:0100555	Asymmetric growth
HP:0100556	Hemiatrophy
HP:0100557	Hemiatrophy of lower limb
HP:0100558	Hemiatrophy of upper limb
HP:0100559	Lower limb asymmetry
HP:0100560	Upper limb asymmetry
HP:0100561	Spinal cord lesion
HP:0100562	Diplomyelia
HP:0100563	Diastomatomyelia
HP:0100564	Triplomyelia
HP:0100565	Hydromyelia
HP:0100566	Amyelia
HP:0100568	Neoplasm of the endocrine system
HP:0100569	Abnormally ossified vertebrae
HP:0100570	Carcinoid tumor
HP:0100571	Cardiac diverticulum
HP:0100572	Fibrous cardiac diverticulum
HP:0100573	Muscular cardiac diverticulum
HP:0100574	Biliary tract neoplasm
HP:0100575	Neoplasm of the gallbladder
HP:0100576	Amaurosis fugax
HP:0100577	Urinary bladder inflammation
HP:0100578	Lipoatrophy
HP:0100579	Mucosal telangiectasiae
HP:0100580	Barrett esophagus
HP:0100581	Dilatation of renal calices
HP:0100582	Nasal polyposis
HP:0100583	Corneal perforation
HP:0100584	Endocarditis
HP:0100585	Telangiectasia of the skin
HP:0100586	Aseptic leukocyturia
HP:0100587	Abnormality of the preputium
HP:0100588	Paraphimosis
HP:0100589	Urogenital fistula
HP:0100590	Rectal fistula
HP:0100592	Peritoneal abscess
HP:0100593	Calcification of cartilage
HP:0100594	Esophageal web
HP:0100595	Camptocormia
HP:0100596	Absent nares
HP:0100598	Pulmonary edema
HP:0100599	Bifid penis
HP:0100600	Penoscrotal transposition
HP:0100601	Eclampsia
HP:0100602	Preeclampsia
HP:0100603	Toxemia of pregnancy
HP:0100604	Neoplasm of the lip
HP:0100605	Neoplasm of the larynx
HP:0100606	Neoplasm of the respiratory system
HP:0100607	Dysmenorrhea
HP:0100608	Metrorrhagia
HP:0100609	obsolete Hypermenorrhea
HP:0100610	Maternal hyperphenylalaninemia
HP:0100611	Multiple glomerular cysts
HP:0100612	Odontogenic neoplasm
HP:0100613	Death in early adulthood
HP:0100614	Myositis
HP:0100615	Ovarian neoplasm
HP:0100616	Testicular teratoma
HP:0100617	Testicular seminoma
HP:0100618	Leydig cell neoplasia
HP:0100619	Sertoli cell neoplasm
HP:0100620	Germinoma
HP:0100621	Dysgerminoma
HP:0100622	Maternal seizures
HP:0100623	Abnormality of corpus cavernosum
HP:0100624	Corpus cavernosum sclerosis
HP:0100625	Enlarged thorax
HP:0100626	Chronic hepatic failure
HP:0100627	Displacement of the urethral meatus
HP:0100628	Esophageal diverticulum
HP:0100629	Midline facial cleft
HP:0100630	Neoplasia of the nasopharynx
HP:0100631	Neoplasm of the adrenal gland
HP:0100632	Pulmonary sequestration
HP:0100633	Esophagitis
HP:0100634	Neuroendocrine neoplasm
HP:0100635	Carotid paraganglioma
HP:0100636	Pulmonary paraglioma
HP:0100637	obsolete Neoplasia of the nose
HP:0100638	Neoplasm of the pharynx
HP:0100639	Erectile abnormalities
HP:0100640	Laryngeal cyst
HP:0100641	Neoplasm of the adrenal cortex
HP:0100642	Neoplasm of the adrenal medulla
HP:0100643	Abnormality of nail color
HP:0100644	Melanonychia
HP:0100645	Cystocele
HP:0100646	Thyroiditis
HP:0100647	Graves disease
HP:0100648	Neoplasm of the tongue
HP:0100649	Neoplasm of the oral cavity
HP:0100650	Vaginal neoplasm
HP:0100651	Type I diabetes mellitus
HP:0100653	Optic neuritis
HP:0100654	Retrobulbar optic neuritis
HP:0100656	Thoracoabdominal wall defect
HP:0100657	Thoracoabdominal eventration
HP:0100658	Cellulitis
HP:0100659	Abnormality of the cerebral vasculature
HP:0100660	Dyskinesia
HP:0100661	Trigeminal neuralgia
HP:0100662	Chondritis
HP:0100663	Synotia
HP:0100665	Angioedema
HP:0100668	Intestinal duplication
HP:0100669	Abnormal pigmentation of the oral mucosa
HP:0100670	Rough bone trabeculation
HP:0100671	Abnormal trabecular bone morphology
HP:0100672	Vaginal hernia
HP:0100673	Vaginal hydrocele
HP:0100674	Vaginal hematocele
HP:0100675	Vaginal pyocele
HP:0100676	Vaginal lymphocele
HP:0100677	Vulval varicose vein
HP:0100678	Premature skin wrinkling
HP:0100679	Lack of skin elasticity
HP:0100681	Esophageal duplication
HP:0100682	Tracheal atresia
HP:0100684	Salivary gland neoplasm
HP:0100685	Abnormal Sharpey fiber morphology
HP:0100686	Enthesitis
HP:0100687	Polyotia
HP:0100689	Decreased corneal thickness
HP:0100690	Mosaic central corneal dystrophy
HP:0100691	Abnormality of the curvature of the cornea
HP:0100692	Increased corneal curvature
HP:0100693	Iridodonesis
HP:0100694	Tibial torsion
HP:0100695	Lipedema
HP:0100697	Neurofibrosarcoma
HP:0100698	Subcutaneous neurofibromas
HP:0100699	Scarring
HP:0100700	Abnormal arachnoid mater morphology
HP:0100701	Abnormal pia mater
HP:0100702	Arachnoid cyst
HP:0100703	Tongue thrusting
HP:0100704	Cerebral visual impairment
HP:0100705	Abnormality of the glial cells
HP:0100706	Abnormality of the oligodendroglia
HP:0100707	Abnormality of the astrocytes
HP:0100708	Abnormality of the microglia
HP:0100709	Reduction of oligodendroglia
HP:0100710	Impulsivity
HP:0100711	Abnormality of the thoracic spine
HP:0100712	Abnormality of the lumbar spine
HP:0100716	Self-injurious behavior
HP:0100717	Abnormality of the cementum
HP:0100718	Uterine rupture
HP:0100719	Lens coloboma
HP:0100720	Hypoplasia of the ear cartilage
HP:0100721	Mediastinal lymphadenopathy
HP:0100723	Gastrointestinal stroma tumor
HP:0100724	Hypercoagulability
HP:0100725	Lichenification
HP:0100726	Kaposi's sarcoma
HP:0100727	Histiocytosis
HP:0100728	Germ cell neoplasia
HP:0100729	Large face
HP:0100730	Bronchogenic cyst
HP:0100731	Transverse facial cleft
HP:0100732	Pancreatic fibrosis
HP:0100733	Neoplasm of the parathyroid gland
HP:0100734	Abnormality of vertebral epiphysis morphology
HP:0100735	Hypertensive crisis
HP:0100736	Abnormal soft palate morphology
HP:0100737	Abnormal hard palate morphology
HP:0100738	Abnormal eating behavior
HP:0100739	Bulimia
HP:0100742	Vascular neoplasm
HP:0100743	Neoplasm of the rectum
HP:0100744	Abnormality of the humeroradial joint
HP:0100745	Abnormality of the humeroulnar joint
HP:0100746	Macrodactyly of finger
HP:0100747	Macrodactyly of toe
HP:0100748	Muscular edema
HP:0100749	Chest pain
HP:0100750	Atelectasis
HP:0100751	Esophageal neoplasm
HP:0100752	Abnormal liver lobulation
HP:0100753	Schizophrenia
HP:0100754	Mania
HP:0100755	Abnormality of salivation
HP:0100757	Pancreatoblastoma
HP:0100758	Gangrene
HP:0100759	Clubbing of fingers
HP:0100760	Clubbing of toes
HP:0100761	Visceral angiomatosis
HP:0100762	Hemobilia
HP:0100763	Abnormality of the lymphatic system
HP:0100764	Lymphangioma
HP:0100765	Abnormality of the tonsils
HP:0100766	Abnormal lymphatic vessel morphology
HP:0100767	Abnormality of the placenta
HP:0100768	Choriocarcinoma
HP:0100769	Synovitis
HP:0100770	Hyperperistalsis
HP:0100771	Hypoperistalsis
HP:0100773	Cartilage destruction
HP:0100774	Hyperostosis
HP:0100775	Dural ectasia
HP:0100776	Recurrent pharyngitis
HP:0100777	Exostoses
HP:0100778	Cryoglobulinemia
HP:0100779	Urogenital sinus anomaly
HP:0100780	Conjunctival hamartoma
HP:0100781	Abnormality of the sacroiliac joint
HP:0100783	Breast aplasia
HP:0100784	Peripheral arteriovenous fistula
HP:0100785	Insomnia
HP:0100786	Hypersomnia
HP:0100787	Prostate neoplasm
HP:0100788	Fused lips
HP:0100789	Torus palatinus
HP:0100790	Hernia
HP:0100792	Acantholysis
HP:0100795	Abnormally straight spine
HP:0100796	Orchitis
HP:0100797	Toenail dysplasia
HP:0100798	Fingernail dysplasia
HP:0100799	Neoplasm of the middle ear
HP:0100800	Aplasia/Hypoplasia of the pancreas
HP:0100801	Pancreatic aplasia
HP:0100802	Malposition of the stomach
HP:0100803	Abnormality of the periungual region
HP:0100804	Ungual fibroma
HP:0100805	obsolete Precocious menopause
HP:0100806	Sepsis
HP:0100807	Long fingers
HP:0100808	Gastric diverticulum
HP:0100809	Scalp tenderness
HP:0100810	Pointed helix
HP:0100811	Aplasia/Hypoplasia of the colon
HP:0100812	Halitosis
HP:0100813	Testicular torsion
HP:0100814	Blue nevus
HP:0100816	Lip hyperpigmentation
HP:0100817	Renovascular hypertension
HP:0100818	Long thorax
HP:0100819	Intestinal fistula
HP:0100820	Glomerulopathy
HP:0100821	Urethrocele
HP:0100822	Rectocele
HP:0100823	Genital hernia
HP:0100825	Cheilitis
HP:0100826	Neoplasm of the nail
HP:0100827	Lymphocytosis
HP:0100828	Increased T cell count
HP:0100829	Galactorrhea
HP:0100830	Round ear
HP:0100831	Abnormality of vitamin K metabolism
HP:0100832	Vitreous floaters
HP:0100833	Neoplasm of the small intestine
HP:0100834	Neoplasm of the large intestine
HP:0100835	Benign neoplasm of the central nervous system
HP:0100836	Malignant neoplasm of the central nervous system
HP:0100837	Atrophodermia vermiculata
HP:0100838	Recurrent cutaneous abscess formation
HP:0100839	Hepatic agenesis
HP:0100840	Aplasia/Hypoplasia of the eyebrow
HP:0100841	Microgastria
HP:0100842	Septo-optic dysplasia
HP:0100843	obsolete Glioblastoma
HP:0100844	Pancreatic fistula
HP:0100845	Anaphylactic shock
HP:0100847	Palmoplantar pustulosis
HP:0100848	Neoplasm of the male external genitalia
HP:0100849	Neoplasm of the scrotum
HP:0100850	Neoplasm of the penis
HP:0100851	Abnormal emotion/affect behavior
HP:0100852	Abnormal fear/anxiety-related behavior
HP:0100853	Hypoplastic areola
HP:0100854	Aplasia of the musculature
HP:0100855	Triceps hypoplasia
HP:0100856	Poorly ossified vertebrae
HP:0100857	Flat sella turcica
HP:0100858	Dilatation of celiac artery
HP:0100859	Dilatation of superior mesenteric artery
HP:0100860	Dilatation of Inferior mesenteric artery
HP:0100861	Sclerotic vertebral body
HP:0100862	Aplasia of the femoral head
HP:0100863	Aplasia of the femoral neck
HP:0100864	Short femoral neck
HP:0100865	Broad ischia
HP:0100866	Short iliac bones
HP:0100867	Duodenal stenosis
HP:0100869	Palmar telangiectasia
HP:0100870	Plantar telangiectasia
HP:0100871	Abnormality of the palm
HP:0100872	Abnormality of the plantar skin of foot
HP:0100874	Thick hair
HP:0100875	Hemimacroglossia
HP:0100876	Infra-orbital crease
HP:0100877	Renal diverticulum
HP:0100878	Enlarged uterus
HP:0100879	Enlarged ovaries
HP:0100880	Nephrogenic rest
HP:0100881	Congenital mesoblastic nephroma
HP:0100882	Fibrous hamartoma
HP:0100883	Chorangioma
HP:0100884	Compensatory scoliosis
HP:0100885	Lateral venous anomaly
HP:0100886	Abnormality of globe location
HP:0100887	Abnormality of globe size
HP:0100888	Interdigital loops
HP:0100889	Abnormality of the ductus choledochus
HP:0100890	Cyst of the ductus choledochus
HP:0100891	Bifid xiphoid process
HP:0100892	Abnormality of the xiphoid process
HP:0100893	Prominent xiphoid process
HP:0100894	Broad xiphoid process
HP:0100896	Rectal polyposis
HP:0100898	Connective tissue nevi
HP:0100899	Sclerosis of finger phalanx
HP:0100900	Sclerosis of the distal phalanx of the 2nd finger
HP:0100901	Sclerosis of the distal phalanx of the 3rd finger
HP:0100902	Sclerosis of the distal phalanx of the 4th finger
HP:0100903	Sclerosis of the distal phalanx of the 5th finger
HP:0100904	Sclerosis of the middle phalanx of the 2nd finger
HP:0100905	Sclerosis of the middle phalanx of the 3rd finger
HP:0100906	Sclerosis of the middle phalanx of the 4th finger
HP:0100907	Sclerosis of the middle phalanx of the 5th finger
HP:0100908	Sclerosis of the proximal phalanx of the 2nd finger
HP:0100909	Sclerosis of the proximal phalanx of the 3rd finger
HP:0100910	Sclerosis of the proximal phalanx of the 4th finger
HP:0100911	Sclerosis of the proximal phalanx of the 5th finger
HP:0100912	Sclerosis of the distal phalanx of the thumb
HP:0100913	Sclerosis of the proximal phalanx of the thumb
HP:0100914	Sclerosis of the 1st metacarpal
HP:0100915	Sclerosis of distal finger phalanx
HP:0100916	Sclerosis of middle finger phalanx
HP:0100917	Sclerosis of proximal finger phalanx
HP:0100918	Sclerosis of 2nd finger phalanx
HP:0100919	Sclerosis of 3rd finger phalanx
HP:0100920	Sclerosis of 4th finger phalanx
HP:0100921	Sclerosis of 5th finger phalanx
HP:0100922	Sclerosis of thumb phalanx
HP:0100923	Clavicular sclerosis
HP:0100924	Sclerosis of toe phalanx
HP:0100925	Sclerosis of foot bone
HP:0100926	Sclerosis of 2nd toe phalanx
HP:0100927	Sclerosis of 3rd toe phalanx
HP:0100928	Sclerosis of 4th toe phalanx
HP:0100929	Sclerosis of 5th toe phalanx
HP:0100930	Sclerosis of hallux phalanx
HP:0100931	Sclerosis of the proximal phalanx of the 2nd toe
HP:0100932	Sclerosis of the proximal phalanx of the 3rd toe
HP:0100933	Sclerosis of the proximal phalanx of the 4th toe
HP:0100934	Sclerosis of the proximal phalanx of the 5th toe
HP:0100935	Sclerosis of the middle phalanx of the 2nd toe
HP:0100936	Sclerosis of the middle phalanx of the 3rd toe
HP:0100937	Sclerosis of the middle phalanx of the 4th toe
HP:0100938	Sclerosis of the middle phalanx of the 5th toe
HP:0100939	Sclerosis of the distal phalanx of the 2nd toe
HP:0100940	Sclerosis of the distal phalanx of the 3rd toe
HP:0100941	Sclerosis of the distal phalanx of the 4th toe
HP:0100942	Sclerosis of the distal phalanx of the 5th toe
HP:0100943	Sclerosis of the proximal phalanx of the hallux
HP:0100944	Sclerosis of the distal phalanx of the hallux
HP:0100945	Sclerosis of the 1st metatarsal
HP:0100946	Sclerosis of proximal toe phalanx
HP:0100947	Sclerosis of middle toe phalanx
HP:0100948	Sclerosis of distal toe phalanx
HP:0100950	Decreased activity of 3-hydroxyacyl-CoA dehydrogenase
HP:0100951	Enlarged fossa interpeduncularis
HP:0100952	Enlarged sylvian cistern
HP:0100953	Enlarged interhemispheric fissure
HP:0100954	Open operculum
HP:0100955	Giant cell granuloma of mandible
HP:0100957	Abnormality of the renal medulla
HP:0100958	Narrow foramen obturatorium
HP:0100959	Dense metaphyseal bands
HP:0100960	Asymmetric ventricles
HP:0100961	Enlarged hippocampus
HP:0100962	Shyness
HP:0100963	Hyperesthesia
HP:0200000	Dysharmonic bone age
HP:0200001	Dysharmonic accelerated bone age
HP:0200003	Splayed epiphyses
HP:0200005	Abnormal shape of the palpebral fissure
HP:0200006	Slanting of the palpebral fissure
HP:0200007	Abnormal size of the palpebral fissures
HP:0200008	Intestinal polyposis
HP:0200011	Abnormal length of corpus callosum
HP:0200012	Short corpus callosum
HP:0200013	Neoplasm of fatty tissue
HP:0200015	Symmetric great toe depigmentation
HP:0200016	Acrokeratosis
HP:0200017	Cerebral white matter agenesis
HP:0200018	Protanomaly
HP:0200020	Corneal erosion
HP:0200021	Down-sloping shoulders
HP:0200022	Choroid plexus papilloma
HP:0200023	Priapism
HP:0200024	Premature chromatid separation
HP:0200025	Mandibular pain
HP:0200026	Ocular pain
HP:0200028	Pretibial myxedema
HP:0200029	Vasculitis in the skin
HP:0200030	Punctate vasculitis skin lesions
HP:0200032	Kayser-Fleischer ring
HP:0200034	Papule
HP:0200035	Skin plaque
HP:0200036	Skin nodule
HP:0200037	Skin vesicle
HP:0200039	Pustule
HP:0200040	Epidermoid cyst
HP:0200041	Skin erosion
HP:0200042	Skin ulcer
HP:0200043	Verrucae
HP:0200044	Porokeratosis
HP:0200046	Cat cry
HP:0200047	Chondritis of pinna
HP:0200048	Cyanotic episode
HP:0200049	Upper limb hypertonia
HP:0200050	Bracket metacarpal epiphyses
HP:0200053	Hemihypotrophy of lower limb
HP:0200054	Foot monodactyly
HP:0200055	Small hand
HP:0200056	Macular scar
HP:0200057	Marcus Gunn pupil
HP:0200058	Angiosarcoma
HP:0200059	Metastatic angiosarcoma
HP:0200063	Colorectal polyposis
HP:0200064	Asymmetry of iris pigmentation
HP:0200065	Chorioretinal degeneration
HP:0200066	Ribbonlike corneal degeneration
HP:0200067	Recurrent spontaneous abortion
HP:0200068	Nonprogressive visual loss
HP:0200070	Peripheral retinal atrophy
HP:0200071	Peripheral vitreoretinal degeneration
HP:0200072	Episodic quadriplegia
HP:0200073	Respiratory insufficiency due to defective ciliary clearance
HP:0200083	Severe limb shortening
HP:0200084	Giant cell hepatitis
HP:0200085	Limb tremor
HP:0200094	Frontal open bite
HP:0200095	Anterior open bite
HP:0200096	Triangular-shaped open mouth
HP:0200097	Oral mucosal blisters
HP:0200098	Absent skin pigmentation
HP:0200099	obsolete Peripheral retinal pigmentation abnormalities
HP:0200101	Decreased/absent ankle reflexes
HP:0200102	Sparse or absent eyelashes
HP:0200104	Absent fifth fingernail
HP:0200105	Absent fifth toenail
HP:0200106	Absent/shortened dynein arms
HP:0200107	Shortened inner dynein arms
HP:0200108	Shortened outer dynein arms
HP:0200109	Absent/shortened outer dynein arms
HP:0200111	Absent stapes head
HP:0200113	Aphalangy of hands and feet
HP:0200114	Metabolic alkalosis
HP:0200116	Distal ileal atresia
HP:0200117	Recurrent upper and lower respiratory tract infections
HP:0200118	Malabsorption of Vitamin B12
HP:0200119	Acute hepatitis
HP:0200120	Chronic active hepatitis
HP:0200122	Atypical or prolonged hepatitis
HP:0200123	Chronic hepatitis
HP:0200124	Chronic hepatitis due to cryptosporidium infection
HP:0200125	Mitochondrial respiratory chain defects
HP:0200126	obsolete Amyloid cardiomyopathy
HP:0200127	Atrial cardiomyopathy
HP:0200128	Biventricular hypertrophy
HP:0200129	obsolete Calcific mitral stenosis
HP:0200133	Lumbosacral meningocele
HP:0200134	Epileptic encephalopathy
HP:0200135	obsolete Macrocephaly due to hydrocephalus
HP:0200136	Oral-pharyngeal dysphagia
HP:0200138	Bilateral choanal atresia/stenosis
HP:0200141	Small, conical teeth
HP:0200143	Megaloblastic erythroid hyperplasia
HP:0200144	obsolete Anaphylactoid purpura
HP:0200146	Mucoid extracellular matrix accumulation
HP:0200147	Neuronal loss in basal ganglia
HP:0200148	Abnormal liver function tests during pregnancy
HP:0200149	CSF lymphocytic pleiocytosis
HP:0200150	Increased serum bile acid concentration during pregnancy
HP:0200151	Cutaneous mastocytosis
HP:0200153	Agenesis of lateral incisor
HP:0200154	Agenesis of mandibular lateral incisor
HP:0200158	Agenesis of permanent mandibular lateral incisor
HP:0200159	Agenesis of primary mandibular lateral incisor
HP:0200160	Agenesis of maxillary incisor
HP:0200161	Agenesis of mandibular incisor
HP:0400000	Tall chin
HP:0400001	Chin with vertical crease
HP:0400002	Extra concha fold
HP:0400003	Focal absence of the external ear
HP:0400004	Long ear
HP:0400005	Short ear
HP:0400007	Polymenorrhea
HP:0400008	Menometrorrhagia
HP:0410000	Abnormality of vomer
HP:0410003	Cleft maxillary alveolus
HP:0410004	obsolete Cleft secondary palate
HP:0410005	Cleft hard palate
HP:0410006	Abnormality of ophthalmic artery
HP:0410007	Abnormality of cartilage morphology
HP:0410008	Abnormality of the peripheral nervous system
HP:0410009	Abnormality of the somatic nervous system
HP:0410010	Abnormality of somatic nerve plexus
HP:0410011	Abnormality of masticatory muscle
HP:0410012	Abnormal mouth floor morphology
HP:0410013	Abnormality of the submandibular region
HP:0410014	Abnormality of ganglion
HP:0410015	Abnormality of ganglion of peripheral nervous system
HP:0410016	Abnormality of cranial ganglion
HP:0410017	Otitis externa
HP:0410018	Recurrent ear infections
HP:0410019	Epigastric pain
HP:0410020	Fish odor
HP:0410021	Musty odor
HP:0410022	Vaginal fish odor
HP:0410023	Abnormal distribution of cell junction proteins in buccal mucosal cells
HP:0410026	Abnormality of the periodontium
HP:0410027	Alveolar bone loss around teeth
HP:0410028	Recurrent oral herpes
HP:0410030	Cleft lip
HP:0410031	Submucous cleft of soft and hard palate
HP:0410032	Cleft of uvula
HP:0410033	Unilateral alveolar cleft of maxilla
HP:0410034	Bilateral alveolar cleft of maxilla
HP:0410035	Abnormal T cell activation
HP:0410042	Abnormal liver morphology
HP:0410043	Abnormal neural tube morphology
HP:0410049	Abnormality of radial ray
HP:0410050	Decreased level of 1,5 anhydroglucitol in serum
HP:0410051	Increased level of 3-hydroxy-3-methylglutaric acid in urine
HP:0410052	Increased level of allantoin in serum
HP:0410053	Increased level of GABA in serum
HP:0410054	Decreased level of GABA in serum
HP:0410055	Decreased level of erythritol in urine
HP:0410056	Decreased level of erythritol in CSF
HP:0410057	Increased level of D-threitol in plasma
HP:0410058	Increased level of D-threitol in CSF
HP:0410059	Increased level of D-threitol in urine
HP:0410060	Decreased level of D-mannose in urine
HP:0410061	Increased level of galactitol in plasma
HP:0410062	Increased level of galactitol in urine
HP:0410063	Increased level of galactonate in red blood cells
HP:0410064	Increased level of galactitol in red blood cells
HP:0410065	Increased level of hippuric acid in blood
HP:0410066	Increased level of hippuric acid in urine
HP:0410067	Increased level of L-fucose in urine
HP:0410068	Increased level of L-glutamic acid in blood
HP:0410069	Increased level of propylene glycol in blood
HP:0410070	Increased level of ribitol in urine
HP:0410071	Increased level of ribitol in CSF
HP:0410072	Increased level of ribose in urine
HP:0410073	Increased level of ribose in CSF
HP:0410074	Increased level of xylitol in urine
HP:0410075	Increased level of xylitol in CSF
HP:0410132	Increased level of L-pyroglutamic acid in urine
HP:0410133	Chronic idiopathic urticaria
HP:0410134	Physical urticaria
HP:0410135	Cold urticaria
HP:0410136	Aquagenic urticaria
HP:0410137	Solar urticaria
HP:0410138	Vibratory urticaria
HP:0410139	Exercise induced anaphylaxis
HP:0410144	Abnormal biotinidase activity
HP:0410145	Decreased biotinidase activity
HP:0410146	Increased biotinidase activity
HP:0410147	Eosinophilic infiltration in the stomach mucosa
HP:0410148	Idiopathic anaphylaxis
HP:0410149	Drug-induced anaphylaxis
HP:0410151	Eosinophilic infiltration of the esophagus
HP:0410152	Eosinophilic microabscess formation in the esophagus
HP:0410153	Increased level of methylsuccinic acid in urine
HP:0410154	Increased level of myristic acid in serum
HP:0410156	Increased level of N-acetylneuraminic acid in urine
HP:0410157	Increased level of N-acetylneuraminic acid in fibroblasts
HP:0410158	Increased level of O-phosphoethanolamine in urine
HP:0410166	Defective interstrand cross-link repair
HP:0410167	Abnormality of the chest musculature
HP:0410168	Abnormality of the back musculature
HP:0410169	Abnormality of the shoulder musculature
HP:0410170	Hippocampal atrophy
HP:0410171	Increased cotinine level
HP:0410172	Blood xenobiotic
HP:0410173	Increased troponin I level in blood
HP:0410174	Increased troponin T level in blood
HP:0410175	Ketonemia
HP:0410176	Abnormal glucose-6-phosphate dehydrogenase level
HP:0410177	Abnormal glucose-6-phosphate dehydrogenase level in blood
HP:0410178	Increased glucose-6-phosphate dehydrogenase level in blood
HP:0410179	Decreased glucose-6-phosphate dehydrogenase level in blood
HP:0410180	Abnormal glucose-6-phosphate dehydrogenase level in dried blood spot
HP:0410181	Increased glucose-6-phosphate dehydrogenase level in dried blood spot
HP:0410182	Decreased glucose-6-phosphate dehydrogenase level in dried blood spot
HP:0410183	Abnormal glucose-6-phosphate dehydrogenase level in leukocytes
HP:0410184	Abnormal glucose-6-phosphate dehydrogenase level in red blood cells
HP:0410185	Abnormal glucose-6-phosphate dehydrogenase level in tissue
HP:0410186	Increased glucose-6-phosphate dehydrogenase level in tissue
HP:0410187	Decreased glucose-6-phosphate dehydrogenase level in tissue
HP:0410188	Decreased glucose-6-phosphate dehydrogenase level in red blood cells
HP:0410189	Increased glucose-6-phosphate dehydrogenase level in red blood cells
HP:0410190	Decreased glucose-6-phosphate dehydrogenase level in leukocytes
HP:0410191	Increased glucose-6-phosphate dehydrogenase level in leukocytes
HP:0410192	Abnormal uridine diphosphate glucose-4-epimerase activity
HP:0410193	Abnormal uridine diphosphate glucose-4-epimerase activity in plasma
HP:0410194	Increased uridine diphosphate glucose-4-epimerase activity in plasma
HP:0410195	Decreased uridine diphosphate glucose-4-epimerase activity in plasma
HP:0410196	Abnormal uridine diphosphate glucose-4-epimerase activity in red blood cells
HP:0410197	Increased uridine diphosphate glucose-4-epimerase activity in red blood cells
HP:0410198	Decreased uridine diphosphate glucose-4-epimerase activity in red blood cells
HP:0410199	Increased CSF urate concentration
HP:0410200	Positive meconium barbiturate test
HP:0410201	Positive hair barbiturate test
HP:0410202	Positive stool barbiturate test
HP:0410203	Positive gastric fluid barbiturate test
HP:0410204	Increased intestinal transit time
HP:0410205	Abnormal circulating nicotinurate level
HP:0410206	Increased circulating nicotinurate level
HP:0410207	Positive methadone plasma/serum test
HP:0410208	Positive plasma/serum cotinine test
HP:0410209	Folate deficiency in CSF
HP:0410210	Abnormal cord blood measurement
HP:0410211	Abnormal blood gas level in cord blood
HP:0410212	Hyperoxemia in cord blood
HP:0410213	Hypoxemia in cord blood
HP:0410214	Hypercapnia in cord blood
HP:0410215	Hypocapnia in cord blood
HP:0410216	Abnormal blood 5-methyltetrahydrofolate level
HP:0410217	Reduced blood 5-methyltetrahydrofolate level
HP:0410218	Hypoplasia of maxilla relative to mandible
HP:0410219	Hypoplasia of mandible relative to maxilla
HP:0410220	Increased anti-dairy protein IgE antibody level
HP:0410221	Increased anti-animal protein IgE antibody level
HP:0410222	Increased anti-seafood IgE antibody level
HP:0410223	Increased anti-dust mite IgE antibody level
HP:0410224	Increased anti-bacteria IgE antibody level
HP:0410225	Increased anti-drug IgE antibody level
HP:0410226	Increased anti-feather IgE antibody level
HP:0410227	Increased anti-food allergen IgE antibody level
HP:0410228	Increased anti-plant based food allergen IgE antibody level
HP:0410229	Increased anti-gluten IgE antibody level
HP:0410230	Increased anti-nut food product IgE antibody level
HP:0410231	Increased anti-egg IgE antibody level
HP:0410232	Increased anti-fungi IgE antibody level
HP:0410233	Increased anti-meat allergen IgE antibody level
HP:0410234	Increased anti-parasite IgE antibody level
HP:0410235	Increased anti-insect IgE antibody level
HP:0410236	Increased anti-venom IgE antibody level
HP:0410238	Increased anti-plant product IgE antibody level
HP:0410239	Positive urine norcotinine test
HP:0410240	Abnormal IgA level
HP:0410241	Abnormal IgE level
HP:0410242	Abnormal IgG level
HP:0410243	Abnormal IgM level
HP:0410244	Abnormal IgD level
HP:0410245	Decreased circulating total IgD
HP:0410246	Increased IgD level
HP:0410247	Increased anti-animal dander IgE antibody level
HP:0410248	Increased anti-house dust IgE antibody level
HP:0410249	Increased anti-alpha-gal IgE antibody level
HP:0410251	Abnormal L-selectin shedding
HP:0410252	Chronic neutropenia
HP:0410253	Chronic neutropenia in myeloid maturation arrest in bone marrow
HP:0410254	Cyclic neutropenia in myeloid maturation arrest in bone marrow
HP:0410255	Transient neutropenia
HP:0410256	Infection associated neutropenia
HP:0410257	Neutrophilia in presence of infection
HP:0410258	Neutrophilia in absence of infection
HP:0410259	Hepatopulmonary fusion
HP:0410260	Asymmetrical gluteal crease
HP:0410261	Wide space between 4th and 5th toe
HP:0410262	Lower cranial nerve dysfunction
HP:0410263	Brain imaging abnormality
HP:0410264	Subglottic hemangioma
HP:0410265	Supraglottic hemangioma
HP:0410266	Visceral hemangioma
HP:0410267	Intestinal hemangioma
HP:0410268	Spleen hemangioma
HP:0410269	Labial hemangioma
HP:0410270	Esophageal hemangioma
HP:0410271	Laryngeal hemangioma
HP:0410272	Vulvar hemangioma
HP:0410273	Retropharyngeal hemangioma
HP:0410274	Paraspinal hemangioma
HP:0410275	Lumbosacral hemangioma
HP:0410276	Supraumbilical raphe
HP:0410277	Sternal pit
HP:0410278	Pituitary gland cyst
HP:0410279	Atrophic pituitary gland
HP:0410280	Pediatric onset
HP:0410281	Dyspepsia
HP:0410282	Abnormal circulating amylase level
HP:0410283	Positive blood acetaminophen test
HP:0410284	Positive norpropoxyphene blood test
HP:0410285	Positive meconium methadone test
HP:0410286	Positive blood molindone test
HP:0430000	Abnormality of the frontal bone
HP:0430002	Abnormality of the lacrimal bone
HP:0430003	Abnormality of the palatine bone
HP:0430004	Frontomalar faciosynostosis
HP:0430005	Abnormality of ethmoid bone
HP:0430006	Ectopic cilia of eyelid
HP:0430007	Symblepharon
HP:0430008	Accessory eyelid
HP:0430009	Hypoplasia of eyelid
HP:0430010	Microblepharia
HP:0430011	Defect of palpebral conjunctiva
HP:0430012	Incomplete ossification of palatine bone
HP:0430013	Absent palatine bone ossification
HP:0430014	Abnormality of musculature of soft palate
HP:0430015	Abnormality of musculature of pharynx
HP:0430016	Abnormality of tensor veli palatini muscle
HP:0430017	Abnormality of uvular muscle
HP:0430018	Abnormality of nasal musculature
HP:0430019	Abnormality of muscle of facial expression
HP:0430020	Abnormality of levator labii superioris alaeque nasi muscle
HP:0430021	Abnormal common carotid artery morphology
HP:0430022	Abnormality of the sphenoid sinus
HP:0430023	Abnormality of the maxillary sinus
HP:0430024	Abnormality of external jugular vein
HP:0430025	Bilateral facial palsy
HP:0430026	Abnormality of the shape of the midface
HP:0430028	Hyperplasia of the maxilla
HP:0430029	Hyperplasia of the premaxilla
HP:0500001	Body odor
HP:0500005	Anal pain
HP:0500006	Urethritis
HP:0500007	Iris flocculi
HP:0500008	Cornea verticillata
HP:0500009	Dysplastic gangliocytoma of the cerebellum
HP:0500010	obsolete Increased cholesterol esters
HP:0500011	Moon facies
HP:0500012	Abnormality of gonadotropin-releasing hormone level
HP:0500013	Lack of gonadotropin-releasing hormone pulsatility
HP:0500014	obsolete Abnormal test result
HP:0500015	Abnormal cardiac test
HP:0500016	Abnormal cardiac MRI
HP:0500017	Abnormal cardiac catheterization
HP:0500018	Abnormal cardiac exercise stress test
HP:0500019	Abnormal resting energy expenditure from metabolic cart test
HP:0500020	Abnormal cardiac biomarker test
HP:0500021	Reduced brain gamma-aminobutyric acid level by MRS
HP:0500022	Abnormal serum dehydroepiandrosterone level
HP:0500023	Shoulder muscle aplasia
HP:0500024	Aplasia of the musculature of the pelvis
HP:0500026	Hypoplasia of the musculature of the pelvis
HP:0500027	Aplastic colon
HP:0500028	Cotton wool plaques
HP:0500030	Abnormal hepatic glycogen storage
HP:0500031	Sclerosis of the carpal bones
HP:0500032	Abnormal neuron branching
HP:0500033	Abnormal natural killer subset distribution
HP:0500034	Nasolacrimal sac obstruction
HP:0500035	Nasolacrimal sac granuloma
HP:0500036	Nasolacrimal sac papilloma
HP:0500037	Nasolacrimal sac epithelial papillary carcinoma
HP:0500039	Conjunctival cicatrization
HP:0500040	Dermolipoma of the conjunctiva
HP:0500041	Myopic astigmatism
HP:0500042	Latent hypermetropia
HP:0500043	Eyelid retraction
HP:0500044	Upper eyelid retraction
HP:0500045	Collier's sign
HP:0500046	Seborrhoeic blepharitis
HP:0500047	Nasolacrimal sac lymphoma
HP:0500048	Delayed canalization of nasolacrimal duct
HP:0500049	Retinopathy of prematurity
HP:0500050	Retinopathy of prematurity stage 1
HP:0500051	Retinopathy of prematurity stage 2
HP:0500052	Retinopathy of prematurity stage 3
HP:0500053	Retinopathy of prematurity stage 4
HP:0500054	Retinopathy of prematurity stage 4a
HP:0500055	Retinopathy of prematurity stage 4b
HP:0500056	Retinopathy of prematurity stage 5
HP:0500057	Retinopathy of prematurity stage 5a
HP:0500058	Retinopathy of prematurity stage 5b
HP:0500059	Retinopathy of prematurity zone I
HP:0500060	Retinopathy of prematurity zone II
HP:0500061	Retinopathy of prematurity zone III
HP:0500062	Retinopathy of prematurity plus
HP:0500063	Retinopathy of prematurity pre-plus
HP:0500064	Retinopathy of prematurity threshold
HP:0500065	Retinopathy of prematurity prethreshold
HP:0500066	Latent myopia
HP:0500069	Paralytic ectropion
HP:0500070	Conjunctival dermolipoma
HP:0500072	Absolute eccentric fixation
HP:0500073	Abnormal ocular alignment
HP:0500074	Dissociated vertical deviation
HP:0500075	Dissociated horizontal deviation
HP:0500076	Alternating hypetropia
HP:0500077	Alternating hyperphoria
HP:0500078	Alternating hypotropia
HP:0500079	Alternating hypophoria
HP:0500081	Pseudophakia
HP:0500086	Optic nerve gray crescent
HP:0500087	Peripapillary atrophy
HP:0500088	Foveal depigmentation
HP:0500089	Optic nerve sheath meningioma
HP:0500090	Periocular capillary hemangioma
HP:0500091	Lymphangioma of the orbit
HP:0500092	Orbital rhabdomyosarcoma
HP:0500093	IgE-mediated food allergy
HP:0500094	Latex allergy
HP:0500095	Food-induced anaphylaxis
HP:0500096	Venom-induced anaphylaxis
HP:0500097	Stool xenobiotic
HP:0500098	Meconium xenobiotic
HP:0500099	Hair xenobiotic
HP:0500100	Plasma/serum xenobiotic
HP:0500101	Gastric fluid xenobiotic
HP:0500104	Decreased diastolic blood pressure
HP:0500105	Decreased systolic blood pressure
HP:0500106	Isolated systolic hypertension
HP:0500107	Isolated diastolic hypotension
HP:0500108	Positive urine cocaine test
HP:0500109	Positive urine barbiturate test
HP:0500110	Positive urine cannabinoid test
HP:0500111	Positive urine benzodiazepines test
HP:0500112	Positive urine amphetamine test
HP:0500113	Positive urine opioid test
HP:0500114	Abnormal stool urobilinogen concentration
HP:0500115	Increased stool urobilinogen concentration
HP:0500116	Positive blood barbiturate test
HP:0500117	Abnormal CSF urate concentration
HP:0500132	Hypovalinemia
HP:0500133	Hypotyrosinemia
HP:0500134	Hypertryptophanemia
HP:0500135	Hypotryptophanemia
HP:0500136	Hypothreoninemia
HP:0500138	Hyperserinemia
HP:0500139	Hypoprolinemia
HP:0500140	Decreased hydroxyprolinemia
HP:0500141	Hypophenylalaninemia
HP:0500142	Hypolysinemia
HP:0500143	Hypoleucinemia
HP:0500144	Hypoisoleucinemia
HP:0500145	Hypohistidinemia
HP:0500147	Hypoglutaminemia
HP:0500148	Abnormality of glutamate metabolism
HP:0500149	Hyperglutamatemia
HP:0500150	Hypoglutamatemia
HP:0500151	Hypercystinemia
HP:0500152	Hypocystinemia
HP:0500153	Hyperargininemia
HP:0500154	Hypoalaninemia
HP:0500155	Abnormality of asparagine metabolism
HP:0500156	Hyperasparaginemia
HP:0500157	Hypoasparaginemia
HP:0500158	Abnormality of aspartate metabolism
HP:0500159	Increased level of aspartic acid
HP:0500160	Abnormality of carnosine metabolism
HP:0500161	Increased level of carnosine in blood
HP:0500162	Decreased level of carnosine in blood
HP:0500163	Hypoornithinemia
HP:0500164	Abnormal blood carbon dioxide level
HP:0500165	Abnormal blood oxygen level
HP:0500166	Abnormal circulating gastrin level
HP:0500167	Hypergastrinemia
HP:0500170	Abnormal concentration of acylcarnitine in the urine
HP:0500173	Reflex asystolic syncope
HP:0550003	Proximal scleroderma
HP:0550004	Verruca plana
HP:0550005	Bilateral basilar pulmonary fibrosis
HP:3000001	obsolete Abnormal heart morphology
HP:3000002	Abnormal inner ear epithelium morphology
HP:3000003	Abnormal mandibular ramus morphology
HP:3000004	Abnormality of frontalis muscle belly
HP:3000005	Abnormality of masseter muscle
HP:3000006	Abnormality of medial pterygoid muscle
HP:3000007	Abnormality of mentalis muscle
HP:3000008	Abnormality of mylohyoid muscle
HP:3000009	Abnormality of nasalis muscle
HP:3000010	Abnormality of orbicularis oris muscle
HP:3000011	Abnormality of palatoglossus muscle
HP:3000012	Abnormality of palatopharyngeus muscle
HP:3000013	Abnormality of platysma
HP:3000014	Abnormality of procerus muscle
HP:3000015	Abnormality of risorius muscle
HP:3000016	Abnormality of styloglossus muscle
HP:3000017	Abnormality of temporalis muscle
HP:3000018	Abnormality of zygomaticus major muscle
HP:3000019	Abnormality of buccal mucosa
HP:3000020	Abnormality of zygomaticus minor muscle
HP:3000021	Abnormality of buccal fat pad
HP:3000022	Abnormality of cartilage of external ear
HP:3000023	Abnormality of angular artery
HP:3000024	Abnormal facial artery morphology
HP:3000025	Abnormality of ciliary ganglion
HP:3000026	obsolete Abnormality of common carotid artery plus branches
HP:3000027	Abnormality of buccinator muscle
HP:3000028	Abnormality of depressor anguli oris muscle
HP:3000029	Abnormality of depressor labii inferioris
HP:3000030	Abnormality of bony orbit of skull
HP:3000031	Abnormality of anterior ethmoidal artery
HP:3000032	Abnormality of central retinal artery
HP:3000033	Abnormality of nasopharyngeal adenoids
HP:3000034	Abnormality of cartilage of nasal septum
HP:3000035	Abnormality of cervical plexus
HP:3000036	Abnormality of head blood vessel
HP:3000037	Abnormality of neck blood vessel
HP:3000038	Abnormal cricoid cartilage morphology
HP:3000039	Abnormality of dorsal nasal artery
HP:3000040	Abnormality of ethmoid sinus
HP:3000041	Abnormality of external carotid artery
HP:3000042	Abnormal jugular vein morphology
HP:3000043	Abnormal facial vein morphology
HP:3000044	Abnormality of frontal process of maxilla
HP:3000045	Abnormality of genioglossus muscle
HP:3000046	Abnormality of geniohyoid muscle
HP:3000047	Abnormal glossopharyngeal nerve morphology
HP:3000048	Abnormal great auricular nerve morphology
HP:3000049	Abnormal greater palatine artery morphology
HP:3000050	Abnormality of odontoid tissue
HP:3000051	Abnormality of hyoglossus muscle
HP:3000052	Abnormality of hyoid bone
HP:3000053	Abnormality of hypopharynx
HP:3000054	Abnormality of inferior alveolar artery
HP:3000055	Abnormality of inferior alveolar nerve
HP:3000056	Abnormality of artery of lower lip
HP:3000057	Abnormality of inferior oblique extraocular muscle
HP:3000058	Abnormality of inferior rectus extraocular muscle
HP:3000059	Abnormal inferior thyroid vein morphology
HP:3000060	Abnormality of infraorbital artery
HP:3000061	Abnormality of infra-orbital nerve
HP:3000062	Abnormal internal carotid artery morphology
HP:3000063	Abnormality of internal jugular vein
HP:3000064	Abnormality of intrinsic muscle of tongue
HP:3000065	Abnormal lacrimal artery morphology
HP:3000066	Abnormal lacrimal sac morphology
HP:3000067	Abnormal lateral cricoarytenoid muscle morphology
HP:3000068	Abnormality of lateral pterygoid muscle
HP:3000069	Abnormality of lateral rectus extra-ocular muscle
HP:3000070	Abnormality of levator anguli oris
HP:3000071	Abnormality of levator labii superioris
HP:3000072	Abnormal levator palpebrae superioris morphology
HP:3000073	Abnormality of levator veli palatini muscle
HP:3000074	Abnormal lingual artery morphology
HP:3000075	Abnormal lingual nerve morphology
HP:3000076	Abnormality of lingual tonsil
HP:3000077	Abnormal mandible condylar process morphology
HP:3000078	Abnormal mandible coronoid process morphology
HP:3000079	Abnormality of mandibular symphysis
