import pytest


@pytest.fixture
def search():
    return {
        "limit": 20,
        "offset": 0,
        "total": 130,
        "items": [
            {
                "id": "MONDO:0019391",
                "category": "biolink:Disease",
                "name": "Fanconi anemia",
                "full_name": None,
                "deprecated": None,
                "description": "Fanconi anemia (FA) is a hereditary DNA repair disorder characterized by progressive pancytopenia with bone marrow failure, variable congenital malformations and predisposition to develop hematological or solid tumors.",
                "xref": [
                    "DOID:13636",
                    "GARD:6425",
                    "ICD9:284.09",
                    "MEDGEN:41967",
                    "MESH:D005199",
                    "MedDRA:10055206",
                    "NANDO:1200303",
                    "NANDO:1200891",
                    "NANDO:2200652",
                    "NCIT:C62505",
                    "NORD:1132",
                    "OMIMPS:227650",
                    "Orphanet:84",
                    "SCTID:30575002",
                    "UMLS:C0015625",
                ],
                "provided_by": "phenio_nodes",
                "in_taxon": None,
                "in_taxon_label": None,
                "symbol": None,
                "synonym": [
                    "Fanconi anemia",
                    "Fanconi pancytopenia",
                    "Fanconi panmyelopathy",
                    "Fanconi's anaemia",
                    "Fanconi's anemia",
                    "Panmyelopathy, Fanconi",
                    "pancytopenia, congenital",
                    "primary erythroid hypoplasia",
                ],
                "broad_synonym": None,
                "exact_synonym": None,
                "narrow_synonym": None,
                "related_synonym": None,
                "subsets": [
                    "clingen",
                    "gard_rare",
                    "nord_rare",
                    "ordo_disorder",
                    "ordo_malformation_syndrome",
                    "orphanet_rare",
                    "otar",
                    "rare",
                ],
                "uri": None,
                "iri": None,
                "namespace": "MONDO",
                "has_phenotype": [
                    "HP:0100867",
                    "HP:0100760",
                    "HP:0100587",
                    "HP:0100542",
                    "HP:0100026",
                    "HP:0040071",
                    "HP:0012639",
                    "HP:0012041",
                    "HP:0010469",
                    "HP:0010293",
                    "HP:0008678",
                    "HP:0000377",
                    "HP:0008053",
                    "HP:0007565",
                    "HP:0006824",
                    "HP:0006265",
                    "HP:0006101",
                    "HP:0005344",
                    "HP:0004349",
                    "HP:0004209",
                    "HP:0003022",
                    "HP:0002863",
                    "HP:0002827",
                    "HP:0002823",
                    "HP:0002575",
                    "HP:0002414",
                    "HP:0002251",
                    "HP:0002245",
                    "HP:0002119",
                    "HP:0002023",
                    "HP:0002007",
                    "HP:0001824",
                    "HP:0001770",
                    "HP:0001763",
                    "HP:0001760",
                    "HP:0001679",
                    "HP:0001646",
                    "HP:0001643",
                    "HP:0001639",
                    "HP:0001636",
                    "HP:0001631",
                    "HP:0001562",
                    "HP:0001537",
                    "HP:0001511",
                    "HP:0001510",
                    "HP:0001392",
                    "HP:0001347",
                    "HP:0001199",
                    "HP:0000864",
                    "HP:0000813",
                    "HP:0000639",
                    "HP:0000582",
                    "HP:0000568",
                    "HP:0000520",
                    "HP:0000518",
                    "HP:0000508",
                    "HP:0000505",
                    "HP:0000504",
                    "HP:0000492",
                    "HP:0000486",
                    "HP:0000483",
                    "HP:0000478",
                    "HP:0000453",
                    "HP:0000365",
                    "HP:0000364",
                    "HP:0000347",
                    "HP:0000340",
                    "HP:0000324",
                    "HP:0000316",
                    "HP:0000286",
                    "HP:0000268",
                    "HP:0000238",
                    "HP:0000218",
                    "HP:0000175",
                    "HP:0000135",
                    "HP:0000130",
                    "HP:0000083",
                    "HP:0000072",
                    "HP:0000047",
                    "HP:0000035",
                    "HP:0000028",
                    "HP:0000027",
                    "HP:0000010",
                    "HP:0012745",
                    "HP:0012210",
                    "HP:0007874",
                    "HP:0002664",
                    "HP:0002650",
                    "HP:0001671",
                    "HP:0001263",
                    "HP:0001249",
                    "HP:0000252",
                    "HP:0000079",
                    "HP:0007400",
                    "HP:0006501",
                    "HP:0005522",
                    "HP:0004322",
                    "HP:0003220",
                    "HP:0002817",
                    "HP:0001903",
                    "HP:0001882",
                    "HP:0001873",
                    "HP:0001871",
                    "HP:0001172",
                    "HP:0001053",
                    "HP:0001000",
                ],
                "has_phenotype_label": [
                    "Duodenal stenosis",
                    "Clubbing of toes",
                    "Abnormal preputium morphology",
                    "Abnormal localization of kidney",
                    "Arteriovenous malformation",
                    "Abnormal morphology of ulna",
                    "Abnormal nervous system morphology",
                    "Decreased fertility in males",
                    "Absent testis",
                    "Aplasia/Hypoplasia of the uvula",
                    "Renal hypoplasia/aplasia",
                    "Abnormal pinna morphology",
                    "Aplasia/Hypoplasia of the iris",
                    "Multiple cafe-au-lait spots",
                    "Cranial nerve paralysis",
                    "Aplasia/Hypoplasia of fingers",
                    "Finger syndactyly",
                    "Abnormal carotid artery morphology",
                    "Reduced bone mineral density",
                    "Clinodactyly of the 5th finger",
                    "Hypoplasia of the ulna",
                    "Myelodysplasia",
                    "Hip dislocation",
                    "Abnormal femur morphology",
                    "Tracheoesophageal fistula",
                    "Spina bifida",
                    "Aganglionic megacolon",
                    "Meckel diverticulum",
                    "Ventriculomegaly",
                    "Anal atresia",
                    "Frontal bossing",
                    "Weight loss",
                    "Toe syndactyly",
                    "Pes planus",
                    "Abnormal foot morphology",
                    "Abnormal aortic morphology",
                    "Abnormal aortic valve morphology",
                    "Patent ductus arteriosus",
                    "Hypertrophic cardiomyopathy",
                    "Tetralogy of Fallot",
                    "Atrial septal defect",
                    "Oligohydramnios",
                    "Umbilical hernia",
                    "Intrauterine growth retardation",
                    "Growth delay",
                    "Abnormality of the liver",
                    "Hyperreflexia",
                    "Triphalangeal thumb",
                    "Abnormality of the hypothalamus-pituitary axis",
                    "Bicornuate uterus",
                    "Nystagmus",
                    "Upslanted palpebral fissure",
                    "Microphthalmia",
                    "Proptosis",
                    "Cataract",
                    "Ptosis",
                    "Visual impairment",
                    "Abnormality of vision",
                    "Abnormal eyelid morphology",
                    "Strabismus",
                    "Astigmatism",
                    "Abnormality of the eye",
                    "Choanal atresia",
                    "Hearing impairment",
                    "Hearing abnormality",
                    "Micrognathia",
                    "Sloping forehead",
                    "Facial asymmetry",
                    "Hypertelorism",
                    "Epicanthus",
                    "Dolichocephaly",
                    "Hydrocephalus",
                    "High palate",
                    "Cleft palate",
                    "Hypogonadism",
                    "Abnormality of the uterus",
                    "Renal insufficiency",
                    "Hydroureter",
                    "Hypospadias",
                    "Abnormal testis morphology",
                    "Cryptorchidism",
                    "Azoospermia",
                    "Recurrent urinary tract infections",
                    "Short palpebral fissure",
                    "Abnormal renal morphology",
                    "Almond-shaped palpebral fissure",
                    "Neoplasm",
                    "Scoliosis",
                    "Abnormal cardiac septum morphology",
                    "Global developmental delay",
                    "Intellectual disability",
                    "Microcephaly",
                    "Abnormality of the urinary system",
                    "Irregular hyperpigmentation",
                    "Aplasia/Hypoplasia of the radius",
                    "Pyridoxine-responsive sideroblastic anemia",
                    "Short stature",
                    "Abnormality of chromosome stability",
                    "Abnormality of the upper limb",
                    "Anemia",
                    "Decreased total leukocyte count",
                    "Thrombocytopenia",
                    "Abnormality of blood and blood-forming tissues",
                    "Abnormal thumb morphology",
                    "Hypopigmented skin patches",
                    "Abnormality of skin pigmentation",
                ],
                "has_phenotype_closure": [
                    "UPHENO:0077874",
                    "HP:0001053",
                    "UPHENO:0077877",
                    "CL:0000457",
                    "UPHENO:0086173",
                    "CL:0000225",
                    "CL:0000151",
                    "UPHENO:0077391",
                    "CL:0000458",
                    "UPHENO:0035160",
                    "UPHENO:0088337",
                    "UPHENO:0063794",
                    "UPHENO:0088319",
                    "HP:0011893",
                    "UPHENO:0087123",
                    "UPHENO:0085371",
                    "UPHENO:0063787",
                    "HP:0001882",
                    "UPHENO:0088166",
                    "HP:0003220",
                    "GO:0008152",
                    "UPHENO:0069254",
                    "HP:0004322",
                    "HP:0001873",
                    "UPHENO:0080352",
                    "UPHENO:0080351",
                    "GO:0009987",
                    "HP:0005522",
                    "GO:0030218",
                    "CL:0000232",
                    "GO:0002262",
                    "GO:0030154",
                    "GO:0048468",
                    "CL:0000988",
                    "GO:0030097",
                    "HP:0001877",
                    "HP:0006501",
                    "HP:0002060",
                    "HP:0007364",
                    "UPHENO:0077373",
                    "HP:0040195",
                    "UPHENO:0075220",
                    "UPHENO:0080200",
                    "GO:0050890",
                    "HP:0011446",
                    "HP:0001249",
                    "HP:0012759",
                    "HP:0002650",
                    "HP:0000925",
                    "HP:0007874",
                    "HP:0200005",
                    "UPHENO:0041462",
                    "UPHENO:0069562",
                    "UPHENO:0075198",
                    "UPHENO:0068941",
                    "UPHENO:0046753",
                    "HP:0200007",
                    "UBERON:0002405",
                    "UPHENO:0002263",
                    "HP:0000010",
                    "HP:0002719",
                    "UBERON:0001968",
                    "UPHENO:0080011",
                    "UPHENO:0008523",
                    "HP:0000025",
                    "UPHENO:0005651",
                    "GO:0019953",
                    "GO:0003006",
                    "UPHENO:0085875",
                    "CL:0000039",
                    "UPHENO:0053298",
                    "CL:0000738",
                    "UPHENO:0077418",
                    "HP:0010978",
                    "CL:0000586",
                    "GO:0048232",
                    "GO:0048871",
                    "GO:0022414",
                    "UBERON:0004054",
                    "GO:0042592",
                    "UPHENO:0005508",
                    "UPHENO:0078452",
                    "CL:0000015",
                    "UPHENO:0052965",
                    "UPHENO:0002599",
                    "HP:0012874",
                    "UPHENO:0053500",
                    "UPHENO:0086201",
                    "UPHENO:0077404",
                    "UPHENO:0053572",
                    "UPHENO:0053644",
                    "UPHENO:0053561",
                    "UPHENO:0053632",
                    "HP:0000028",
                    "UPHENO:0002790",
                    "HP:0032076",
                    "HP:0000795",
                    "UBERON:0001423",
                    "UBERON:0000057",
                    "UBERON:0001333",
                    "UBERON:0001556",
                    "UBERON:0035651",
                    "UBERON:0012241",
                    "UBERON:0036295",
                    "HP:0000072",
                    "UPHENO:0002806",
                    "UPHENO:0076780",
                    "UBERON:0006555",
                    "UPHENO:0002427",
                    "UPHENO:0002442",
                    "UPHENO:0002411",
                    "UPHENO:0002940",
                    "UPHENO:0003056",
                    "UPHENO:0002323",
                    "UPHENO:0066902",
                    "HP:0000202",
                    "UPHENO:0063516",
                    "UPHENO:0081423",
                    "UPHENO:0063518",
                    "UPHENO:0063513",
                    "UPHENO:0063529",
                    "UPHENO:0063520",
                    "UPHENO:0063524",
                    "UPHENO:0063519",
                    "CL:0000408",
                    "UPHENO:0001391",
                    "UPHENO:0015184",
                    "UPHENO:0056230",
                    "UBERON:0000178",
                    "UPHENO:0014865",
                    "UPHENO:0056149",
                    "HP:0000238",
                    "UPHENO:0014351",
                    "UPHENO:0056158",
                    "UPHENO:0075877",
                    "UPHENO:0011572",
                    "UBERON:0005629",
                    "UBERON:0036302",
                    "UPHENO:0085938",
                    "UPHENO:0056333",
                    "UPHENO:0056226",
                    "UPHENO:0011536",
                    "UBERON:0003061",
                    "UPHENO:0056242",
                    "UPHENO:0014291",
                    "UPHENO:0014761",
                    "HP:0011873",
                    "UPHENO:0003207",
                    "UPHENO:0003391",
                    "UPHENO:0056251",
                    "HP:0000268",
                    "UBERON:0000076",
                    "UPHENO:0072332",
                    "UPHENO:0072315",
                    "UPHENO:0001231",
                    "UPHENO:0072293",
                    "UPHENO:0072263",
                    "UPHENO:0072355",
                    "HP:0000286",
                    "UBERON:0000014",
                    "UPHENO:0072415",
                    "UPHENO:0049756",
                    "UPHENO:0004418",
                    "UPHENO:0072359",
                    "UBERON:0001712",
                    "UPHENO:0087928",
                    "UPHENO:0072185",
                    "UPHENO:0072200",
                    "UPHENO:0002864",
                    "UPHENO:0072195",
                    "UPHENO:0002887",
                    "UPHENO:0072194",
                    "UPHENO:0072264",
                    "UPHENO:0084729",
                    "HP:0000324",
                    "UPHENO:0046487",
                    "UPHENO:0041083",
                    "HP:0000277",
                    "UPHENO:0081141",
                    "HP:0030791",
                    "HP:0011821",
                    "HP:0009116",
                    "UPHENO:0002875",
                    "HP:0009118",
                    "UPHENO:0002732",
                    "UBERON:0003278",
                    "HP:0008669",
                    "UPHENO:0081786",
                    "UPHENO:0002942",
                    "UBERON:0012314",
                    "UBERON:0005867",
                    "UPHENO:0002868",
                    "UPHENO:0081314",
                    "UPHENO:0052231",
                    "GO:0050954",
                    "UPHENO:0005513",
                    "UPHENO:0052970",
                    "UPHENO:0005512",
                    "UPHENO:0050625",
                    "UPHENO:0004503",
                    "HP:0000453",
                    "UBERON:0005725",
                    "UPHENO:0086610",
                    "UBERON:0002268",
                    "UPHENO:0003395",
                    "UPHENO:0031226",
                    "UPHENO:0031179",
                    "UPHENO:0031129",
                    "HP:0000135",
                    "UPHENO:0031142",
                    "UPHENO:0004764",
                    "UPHENO:0031144",
                    "UPHENO:0031228",
                    "UPHENO:0041037",
                    "UPHENO:0031123",
                    "HP:0000483",
                    "HP:0001263",
                    "UPHENO:0041079",
                    "UBERON:0010222",
                    "HP:0000486",
                    "UPHENO:0050236",
                    "UPHENO:0052164",
                    "UPHENO:0049904",
                    "GO:0007601",
                    "UPHENO:0050620",
                    "GO:0007600",
                    "UPHENO:0001392",
                    "HP:0000347",
                    "UPHENO:0052159",
                    "UPHENO:0041667",
                    "UPHENO:0041644",
                    "UPHENO:0041410",
                    "UBERON:0000965",
                    "UPHENO:0084815",
                    "HP:0000517",
                    "UPHENO:0004765",
                    "HP:0000518",
                    "HP:0100886",
                    "UPHENO:0018424",
                    "UPHENO:0075219",
                    "HP:0000568",
                    "HP:0000240",
                    "UBERON:0001711",
                    "HP:0000582",
                    "HP:0100627",
                    "UBERON:0000056",
                    "HP:0000365",
                    "HP:0200006",
                    "HP:0000492",
                    "UPHENO:0033591",
                    "HP:0030669",
                    "UPHENO:0005319",
                    "HP:0012373",
                    "HP:0000639",
                    "UPHENO:0079828",
                    "UPHENO:0005517",
                    "UPHENO:0002352",
                    "UPHENO:0005636",
                    "UBERON:0010425",
                    "UPHENO:0002219",
                    "UPHENO:0005022",
                    "UPHENO:0085302",
                    "UBERON:0000474",
                    "UPHENO:0063514",
                    "UPHENO:0087806",
                    "UPHENO:0002687",
                    "UPHENO:0005170",
                    "UBERON:0003975",
                    "UPHENO:0041151",
                    "NBO:0000417",
                    "UPHENO:0003053",
                    "UBERON:0013515",
                    "UPHENO:0041395",
                    "UPHENO:0004709",
                    "UBERON:0000995",
                    "HP:0000864",
                    "HP:0001172",
                    "UBERON:0010688",
                    "UBERON:5106048",
                    "UBERON:5102389",
                    "HP:0001939",
                    "UBERON:0012151",
                    "UBERON:0006048",
                    "UBERON:5006048",
                    "UBERON:0003620",
                    "UBERON:0012358",
                    "UBERON:0015025",
                    "UBERON:5101463",
                    "UPHENO:0003069",
                    "UBERON:5001463",
                    "GO:0050896",
                    "HP:0001347",
                    "UPHENO:0055094",
                    "UPHENO:0080187",
                    "UPHENO:0049703",
                    "UPHENO:0049586",
                    "NBO:0000389",
                    "GO:0050881",
                    "GO:0050877",
                    "UPHENO:0050079",
                    "GO:0003008",
                    "UPHENO:0031124",
                    "GO:0009605",
                    "NBO:0000388",
                    "UPHENO:0050606",
                    "UPHENO:0049699",
                    "UPHENO:0050613",
                    "HP:0031826",
                    "UPHENO:0077348",
                    "UPHENO:0049708",
                    "UBERON:0002107",
                    "UPHENO:0002780",
                    "UBERON:0002423",
                    "UBERON:0000949",
                    "UPHENO:0072345",
                    "UBERON:0002330",
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                    "HP:0001392",
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                    "UBERON:0002368",
                    "UBERON:0002365",
                    "UBERON:0006925",
                    "NBO:0000403",
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                    "UPHENO:0052160",
                    "UPHENO:0050068",
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                    "UPHENO:0080382",
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                    "HP:0001551",
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                    "UBERON:0017672",
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                    "HP:0025633",
                    "UPHENO:0033603",
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                    "UBERON:0006876",
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                    "UBERON:0000179",
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                    "UPHENO:0086172",
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                    "UPHENO:0087070",
                    "UPHENO:0005080",
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                    "UBERON:0002082",
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                    "UPHENO:0004403",
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                    "UBERON:0004140",
                    "UPHENO:0056250",
                    "UBERON:0036146",
                    "UPHENO:0088118",
                    "UBERON:0004145",
                    "UPHENO:0004405",
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                    "UBERON:0007100",
                    "HP:0001671",
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                    "UBERON:0003084",
                    "HP:0010460",
                    "UBERON:0004139",
                    "UBERON:0004872",
                    "UPHENO:0005177",
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                    "HP:0001627",
                    "NBO:0000001",
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                    "UBERON:0003519",
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                    "HP:0001679",
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                    "HP:0000130",
                    "HP:0001763",
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                    "UPHENO:0069119",
                    "HP:0009122",
                    "HP:0100691",
                    "UPHENO:0041041",
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                    "HP:0001770",
                    "UPHENO:0078375",
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                    "UPHENO:0010795",
                    "CL:0000255",
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                    "HP:0001824",
                    "HP:0001507",
                    "UPHENO:0054374",
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                    "UBERON:1000021",
                    "UPHENO:0010808",
                    "UPHENO:0054315",
                    "UPHENO:0049874",
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                    "HP:0001384",
                    "UPHENO:0086091",
                    "UPHENO:0063621",
                    "UPHENO:0004149",
                    "HP:0025028",
                    "UPHENO:0076728",
                    "HP:0032039",
                    "UPHENO:0087980",
                    "UPHENO:0002576",
                    "UBERON:0002217",
                    "UBERON:0001272",
                    "UBERON:0010428",
                    "UPHENO:0004094",
                    "UBERON:0007832",
                    "UPHENO:0002728",
                    "UPHENO:0004143",
                    "HP:0100491",
                    "UBERON:0000982",
                    "UPHENO:0003052",
                    "UBERON:0007828",
                    "UPHENO:0076735",
                    "HP:0002644",
                    "UBERON:0008114",
                    "UBERON:0004381",
                    "UPHENO:0086486",
                    "UBERON:0007830",
                    "UBERON:0008811",
                    "UBERON:0001005",
                    "HP:0000083",
                    "HP:0002823",
                    "UBERON:0000117",
                    "UBERON:0005893",
                    "UPHENO:0086614",
                    "UPHENO:0068912",
                    "UPHENO:0087367",
                    "UBERON:0000075",
                    "HP:0040069",
                    "UBERON:0003947",
                    "HP:0002086",
                    "UPHENO:0063581",
                    "UPHENO:0002952",
                    "UBERON:0001043",
                    "UBERON:0000065",
                    "UPHENO:0014292",
                    "UPHENO:0087433",
                    "UPHENO:0076761",
                    "HP:0001710",
                    "HP:0002778",
                    "UPHENO:0076785",
                    "UBERON:0010191",
                    "UBERON:0004119",
                    "UBERON:0001004",
                    "UPHENO:0087662",
                    "UBERON:0000072",
                    "UPHENO:0002634",
                    "UPHENO:0033565",
                    "UPHENO:0053330",
                    "UPHENO:0046403",
                    "UBERON:0005178",
                    "UBERON:0010230",
                    "UBERON:0003126",
                    "UBERON:0003258",
                    "CL:0000329",
                    "UPHENO:0081788",
                    "UBERON:0004128",
                    "UPHENO:0005257",
                    "UBERON:0001021",
                    "UPHENO:0076752",
                    "GO:0060429",
                    "UPHENO:0002734",
                    "HP:0005607",
                    "UBERON:0000059",
                    "UPHENO:0003086",
                    "UPHENO:0002246",
                    "UPHENO:0003084",
                    "UBERON:0002075",
                    "UBERON:0005911",
                    "UPHENO:0086965",
                    "UPHENO:0002813",
                    "UPHENO:0011557",
                    "UPHENO:0002527",
                    "UPHENO:0041664",
                    "HP:0004298",
                    "UBERON:0000489",
                    "UPHENO:0051003",
                    "HP:0000252",
                    "HP:0001562",
                    "UBERON:0004086",
                    "UBERON:0008001",
                    "UPHENO:0049966",
                    "UPHENO:0082875",
                    "UBERON:0002329",
                    "UBERON:0005174",
                    "UBERON:0007530",
                    "GO:0034101",
                    "HP:0045005",
                    "GO:0002009",
                    "HP:0030680",
                    "UPHENO:0003234",
                    "UPHENO:0003191",
                    "UPHENO:0080369",
                    "UBERON:0011585",
                    "GO:0035148",
                    "UPHENO:0087369",
                    "GO:0048598",
                    "UBERON:0015024",
                    "UBERON:0004876",
                    "GO:0048729",
                    "GO:0048869",
                    "GO:0035239",
                    "UPHENO:0033612",
                    "UPHENO:0004509",
                    "UPHENO:0076773",
                    "HP:0004328",
                    "HP:0012848",
                    "UPHENO:0002957",
                    "UPHENO:0086482",
                    "UPHENO:0033593",
                    "UBERON:0010741",
                    "UPHENO:0002767",
                    "UPHENO:0052675",
                    "UBERON:0002137",
                    "UBERON:0007285",
                    "HP:0000508",
                    "UPHENO:0033599",
                    "UPHENO:0087510",
                    "UPHENO:0002694",
                    "HP:0008053",
                    "UPHENO:0003038",
                    "HP:0031816",
                    "UBERON:0002342",
                    "UBERON:0003077",
                    "UBERON:0003056",
                    "UBERON:0003059",
                    "UBERON:0002472",
                    "GO:0009792",
                    "UPHENO:0080662",
                    "GO:0007399",
                    "UPHENO:0004881",
                    "UPHENO:0003550",
                    "UBERON:0001809",
                    "GO:0072175",
                    "HP:0000818",
                    "UPHENO:0051276",
                    "UPHENO:0002880",
                    "GO:0060606",
                    "UPHENO:0075655",
                    "UPHENO:0050234",
                    "UPHENO:0002595",
                    "UPHENO:0002537",
                    "UBERON:0001130",
                    "GO:0007275",
                    "GO:0009888",
                    "UPHENO:0031125",
                    "UPHENO:0002804",
                    "GO:0035295",
                    "UBERON:0011215",
                    "UPHENO:0076695",
                    "UBERON:0007844",
                    "UPHENO:0002638",
                    "UPHENO:0087858",
                    "GO:0048856",
                    "UBERON:0005856",
                    "UPHENO:0081436",
                    "UPHENO:0002682",
                    "UPHENO:0003182",
                    "GO:0001838",
                    "UPHENO:0087846",
                    "UPHENO:0002976",
                    "HP:0002414",
                    "UPHENO:0072255",
                    "UPHENO:0002301",
                    "UPHENO:0002543",
                    "UPHENO:0076791",
                    "UBERON:0001137",
                    "UBERON:0015061",
                    "HP:0002251",
                    "HP:0000008",
                    "UBERON:0002410",
                    "GO:0007276",
                    "UBERON:0015023",
                    "UBERON:0003338",
                ],
                "has_phenotype_closure_label": [
                    "decreased biological_process in multicellular organism",
                    "Hypopigmentation of the skin",
                    "Thrombocytopenia",
                    "number of platelet phenotype",
                    "biogenic amine secreting cell",
                    "platelet phenotype",
                    "secretory cell",
                    "decreased number of platelet",
                    "decreased number of anatomical structure in the multicellular organism",
                    "Decreased total leukocyte count",
                    "leukocyte morphology phenotype",
                    "decreased number of material anatomical entity",
                    "Abnormal leukocyte count",
                    "decreased number of cell",
                    "decreased number of leukocyte in the blood",
                    "decreased number of anatomical entity",
                    "decreased number of material anatomical entity in the multicellular organism",
                    "decreased number of hematopoietic cell",
                    "Abnormal cellular immune system morphology",
                    "decreased number of leukocyte",
                    "homeostatic process phenotype",
                    "Abnormal cellular phenotype",
                    "size of multicellular organism phenotype",
                    "multicellular organism height phenotype",
                    "decreased height of the anatomical entity",
                    "Sideroblastic anemia",
                    "cellular process",
                    "Anemia",
                    "myeloid cell differentiation",
                    "erythrocyte homeostasis",
                    "number of myeloid cell phenotype",
                    "cell differentiation",
                    "homeostatic process",
                    "cellular developmental process",
                    "multicellular organismal-level homeostasis",
                    "myeloid cell homeostasis",
                    "radius bone morphology phenotype",
                    "Aplasia/Hypoplasia of the radius",
                    "aplasia or hypoplasia of radius bone",
                    "aplasia or hypoplasia of telencephalon",
                    "Aplasia/Hypoplasia involving the central nervous system",
                    "size of skull phenotype",
                    "Aplasia/Hypoplasia of the cerebrum",
                    "Abnormal cerebral morphology",
                    "Abnormality of mental function",
                    "cognition",
                    "Neurodevelopmental delay",
                    "Neurodevelopmental abnormality",
                    "Abnormality of the vertebral column",
                    "Abnormal curvature of the vertebral column",
                    "Scoliosis",
                    "Almond-shaped palpebral fissure",
                    "Abnormal shape of the palpebral fissure",
                    "shape of palpebral fissure phenotype",
                    "decreased size of the orifice",
                    "Abnormal size of the palpebral fissures",
                    "Short palpebral fissure",
                    "decreased length of anatomical conduit",
                    "Unusual infection",
                    "Recurrent urinary tract infections",
                    "Recurrent infections",
                    "internal male genitalia phenotype",
                    "number of sperm phenotype",
                    "absent sperm in the semen",
                    "absent sperm",
                    "Intellectual disability",
                    "decreased male gamete generation",
                    "number of cell phenotype",
                    "decreased reproductive process",
                    "absent anatomical entity in the semen",
                    "decreased spermatogenesis",
                    "spermatogenesis",
                    "gamete",
                    "decreased developmental process involved in reproduction",
                    "absent germ cell",
                    "internal male genitalia",
                    "germ line cell",
                    "haploid cell",
                    "Functional abnormality of male internal genitalia",
                    "decreased multicellular organismal reproductive process",
                    "localised anatomical structure",
                    "localised multicellular anatomical structure",
                    "testis phenotype",
                    "Cryptorchidism",
                    "localised material anatomical entity",
                    "lower urinary tract phenotype",
                    "male urethral meatus",
                    "urethral opening",
                    "decreased number of anatomical entity in the blood",
                    "Abnormality of the lower urinary tract",
                    "lower urinary tract",
                    "excretory tube",
                    "renal pelvis/ureter",
                    "Abnormal ureter morphology",
                    "excretory tube phenotype",
                    "Hydroureter",
                    "ureter",
                    "ureter morphology phenotype",
                    "abdominal segment element physiology phenotype",
                    "cavitated compound organ physiology phenotype",
                    "decreased functionality of the reproductive structure",
                    "reproductive structure physiology phenotype",
                    "decreased functionality of the gonad",
                    "reproductive organ physiology phenotype",
                    "Cleft palate",
                    "Orofacial cleft",
                    "incomplete closing of the ectoderm-derived structure",
                    "increased height of the structure with developmental contribution from neural crest",
                    "increased size of the structure with developmental contribution from neural crest",
                    "decreased functionality of the organ",
                    "anatomical entity height phenotype",
                    "increased height of the anatomical structure",
                    "increased height of the multicellular anatomical structure",
                    "High palate",
                    "increased height of the multi-tissue structure",
                    "bodily fluid",
                    "increased number of organ part in the cerebrospinal fluid",
                    "absent anatomical structure",
                    "number of anatomical enitites of type anatomical entity phenotype",
                    "blood",
                    "Abnormal cerebrospinal fluid morphology",
                    "urethra phenotype",
                    "haemolymphatic fluid phenotype",
                    "increased number of anatomical entity",
                    "blood phenotype",
                    "increased number of anatomical structure",
                    "increased number of brain ventricle",
                    "number of anatomical enitites of type organ part phenotype",
                    "blood island phenotype",
                    "developmental process involved in reproduction phenotype",
                    "cerebrospinal fluid",
                    "blood island",
                    "Hydrocephalus",
                    "bodily fluid phenotype",
                    "increased number of brain ventricle/choroid plexus in the cerebrospinal fluid",
                    "vascular plexus",
                    "increased number of ventricle of nervous system in the cerebrospinal fluid",
                    "cerebrospinal fluid phenotype",
                    "increased number of anatomical structure in the cerebrospinal fluid",
                    "number of anatomical enitites of type ectoderm-derived structure phenotype",
                    "number of anatomical enitites of type material anatomical entity phenotype",
                    "Abnormal leukocyte morphology",
                    "Epicanthus",
                    "skin of face",
                    "increased length of the zone of organ",
                    "renal system physiology phenotype",
                    "skin of face morphology phenotype",
                    "increased length of the multicellular anatomical structure",
                    "increased length of the material anatomical entity",
                    "head or neck skin",
                    "increased length of the anatomical structure",
                    "compound organ physiology phenotype",
                    "increased length of the head or neck skin",
                    "increased length of the zone of skin",
                    "increased length of the anatomical line",
                    "increased size of the non-material anatomical boundary",
                    "Hypertelorism",
                    "asymmetry of face phenotype",
                    "Facial asymmetry",
                    "asymmetry of anatomical entity phenotype",
                    "shape of forehead phenotype",
                    "mandible morphology phenotype",
                    "nucleate cell",
                    "increased height of the material anatomical entity",
                    "skeleton of lower jaw phenotype",
                    "increased height of the anatomical entity",
                    "oral opening",
                    "bone of jaw",
                    "aplasia or hypoplasia of mandible",
                    "Abnormal jaw morphology",
                    "aplasia or hypoplasia of skull",
                    "facial bone",
                    "dentary phenotype",
                    "Abnormal mandible morphology",
                    "bone element hypoplasia in face",
                    "bone of lower jaw",
                    "Aplasia/hypoplasia affecting bones of the axial skeleton",
                    "mandibular prominence morphology phenotype",
                    "Micrognathia",
                    "Abnormal facial skeleton morphology",
                    "Displacement of the urethral meatus",
                    "Aplasia/Hypoplasia involving bones of the skull",
                    "Aplasia/Hypoplasia of the mandible",
                    "facial bone hypoplasia",
                    "sensory perception of mechanical stimulus phenotype",
                    "ear physiology phenotype",
                    "Hearing abnormality",
                    "sensory perception of sound phenotype",
                    "decreased qualitatively sensory perception of mechanical stimulus",
                    "increased size of the multi-tissue structure",
                    "posterior nasal aperture phenotype",
                    "posterior nasal aperture",
                    "olfactory system",
                    "Abnormal platelet morphology",
                    "Choanal atresia",
                    "internal naris atresia",
                    "Abnormal nasal morphology",
                    "naris atresia",
                    "Abnormality of the nose",
                    "chemosensory system",
                    "olfactory organ phenotype",
                    "posterior nasal aperture atresia",
                    "Astigmatism",
                    "curved anatomical entity",
                    "Abnormal platelet count",
                    "neural crest-derived structure, curved phenotype",
                    "structure with developmental contribution from neural crest, curved phenotype",
                    "Abnormality of refraction",
                    "decreased gamete generation",
                    "material anatomical entity, asymmetrically curved phenotype",
                    "multicellular anatomical structure, curved phenotype",
                    "cornea phenotype",
                    "Microcephaly",
                    "anatomical structure, curved phenotype",
                    "shape of cornea phenotype",
                    "cornea",
                    "Strabismus",
                    "anatomical line between pupils",
                    "anatomical line",
                    "Craniofacial cleft",
                    "sensory perception phenotype",
                    "Abnormality of vision",
                    "decreased qualitatively visual perception",
                    "Visual impairment",
                    "decreased qualitatively sensory perception",
                    "sensory perception of light stimulus phenotype",
                    "male reproductive system physiology phenotype",
                    "drooping eyelid",
                    "lens of camera-type eye phenotype",
                    "opaque anatomical entity",
                    "localised gonad",
                    "increased number of multicellular anatomical structure",
                    "opaque lens of camera-type eye",
                    "lens of camera-type eye morphology phenotype",
                    "Proptosis",
                    "size of eyeball of camera-type eye phenotype",
                    "increased length of the immaterial anatomical entity",
                    "Microphthalmia",
                    "decreased size of the ectoderm-derived structure",
                    "Abnormality of globe size",
                    "decreased size of the eyeball of camera-type eye",
                    "decreased size of the sense organ",
                    "palpebral fissure phenotype",
                    "Slanting of the palpebral fissure",
                    "Abnormal eyelid morphology",
                    "immune system",
                    "ocular adnexa",
                    "Abnormality of the ocular adnexa",
                    "facial bone phenotype",
                    "eyelid phenotype",
                    "vestibulo-ocular reflex phenotype",
                    "Nystagmus",
                    "Abnormal erythrocyte morphology",
                    "Abnormal involuntary eye movements",
                    "camera-type eye physiology phenotype",
                    "organ physiology phenotype",
                    "vestibulo-ocular reflex",
                    "localised anatomical entity",
                    "Abnormal eye physiology",
                    "increased length of the skin of head",
                    "internal genitalia",
                    "homeostasis of number of cells",
                    "subdivision of oviduct phenotype",
                    "subdivision of oviduct",
                    "female reproductive system phenotype",
                    "bicornuate uterus",
                    "Abnormal morphology of female internal genitalia",
                    "increased number of material anatomical entity in the cerebrospinal fluid",
                    "female organism",
                    "female reproductive organ morphology phenotype",
                    "female reproductive system",
                    "absent material anatomical entity in the multicellular organism",
                    "bone of lower jaw phenotype",
                    "internal female genitalia phenotype",
                    "leukocyte",
                    "uterus morphology phenotype",
                    "shape of uterus phenotype",
                    "internal genitalia phenotype",
                    "Bicornuate uterus",
                    "oviduct phenotype",
                    "absent material anatomical entity",
                    "upper eyelid",
                    "Abnormality of the female genitalia",
                    "Abnormal internal genitalia",
                    "uterus phenotype",
                    "hypothalamus-pituitary axis phenotype",
                    "Abnormality of the endocrine system",
                    "ocular surface region morphology phenotype",
                    "Abnormality of thumb phalanx",
                    "manual digit 1 morphology phenotype",
                    "manual digitopodium bone",
                    "manus bone",
                    "manual digit phalanx endochondral element",
                    "digit 1 digitopodial skeleton",
                    "manual digit digitopodial skeleton",
                    "Dolichocephaly",
                    "manual digit 1 plus metapodial segment",
                    "Triphalangeal thumb",
                    "digit 1 plus metapodial segment",
                    "voluntary musculoskeletal movement phenotype",
                    "response to stimulus phenotype",
                    "number of hematopoietic cell phenotype",
                    "phalanx of manus",
                    "increased reflex",
                    "reflexive behavior",
                    "vascular plexus phenotype",
                    "voluntary movement behavior phenotype",
                    "response to stimulus",
                    "increased number of material anatomical entity",
                    "behavior process phenotype",
                    "increased response to external stimulus",
                    "neuromuscular process phenotype",
                    "neuromuscular process",
                    "kinesthetic behavior",
                    "nervous system process",
                    "multicellular organismal movement",
                    "behavior",
                    "response to external stimulus",
                    "body part movement",
                    "radius bone phenotype",
                    "endocrine gland",
                    "liver phenotype",
                    "internal female genitalia morphology phenotype",
                    "digestive system gland phenotype",
                    "increased length of the organ part",
                    "glandular system",
                    "Abnormality of the liver",
                    "delayed growth",
                    "Abnormal male urethral meatus morphology",
                    "Hypogonadism",
                    "developmental process rate phenotype",
                    "decreased qualitatively embryo development",
                    "decreased qualitatively multicellular organismal process",
                    "decreased qualitatively developmental process",
                    "decreased multicellular organismal process",
                    "decreased embryo development",
                    "decreased qualitatively multicellular organism development",
                    "decreased developmental process",
                    "multicellular organismal process phenotype",
                    "Growth delay",
                    "Hernia of the abdominal wall",
                    "connective tissue phenotype",
                    "Abdominal wall defect",
                    "physiologic nystagmus",
                    "incomplete closing of the organ part",
                    "Hernia",
                    "abdominal wall",
                    "Abnormality of the abdominal wall",
                    "abdominal viscera",
                    "Abnormal umbilicus morphology",
                    "exocrine system",
                    "Abnormality of connective tissue",
                    "decreased length of palpebral fissure",
                    "neural crest-derived structure, asymmetrically curved phenotype",
                    "incomplete closing of the abdominal wall",
                    "amniotic fluid",
                    "late embryo",
                    "Upslanted palpebral fissure",
                    "late embryo phenotype",
                    "embryonic development/birth phenotype",
                    "umbilicus",
                    "amniotic fluid phenotype",
                    "Abnormal cellular physiology",
                    "Abnormality of prenatal development or birth",
                    "organism substance",
                    "decreased sensory perception",
                    "Abnormal uterus morphology",
                    "septum",
                    "incomplete closing of the cardiac septum",
                    "cardiac atrium phenotype",
                    "cardiac septum morphology phenotype",
                    "anatomical structure development phenotype",
                    "interatrial septum morphology phenotype",
                    "cardiac septum phenotype",
                    "cardiac atrium",
                    "Abnormal cardiac septum morphology",
                    "sloped forehead",
                    "Tetralogy of Fallot",
                    "Conotruncal defect",
                    "anatomical entity hypoplasia in face",
                    "liver",
                    "decreased functionality of the organ part",
                    "organ part physiology phenotype",
                    "mesoderm-derived structure physiology phenotype",
                    "non-material anatomical boundary",
                    "myocardium",
                    "multicellular anatomical structure physiology phenotype",
                    "Renal insufficiency",
                    "myocardium morphology phenotype",
                    "Abnormal myocardium morphology",
                    "layer of muscle tissue",
                    "decreased functionality of the material anatomical entity",
                    "decreased functionality of the anatomical entity",
                    "decreased functionality of the mesoderm-derived structure",
                    "response to external stimulus phenotype",
                    "heart layer phenotype",
                    "layer of muscle tissue phenotype",
                    "increased length of the skin of face",
                    "decreased functionality of the myocardium",
                    "musculoskeletal movement phenotype",
                    "decreased functionality of the organ component layer",
                    "anatomical entity dysfunction in independent continuant",
                    "gamete generation",
                    "Abnormal ocular adnexa morphology",
                    "decreased functionality of the anatomical structure",
                    "myocardium phenotype",
                    "incomplete closing of the trunk blood vessel",
                    "coronary vessel",
                    "trunk blood vessel phenotype",
                    "anatomical structure morphology in the heart phenotype",
                    "cell phenotype",
                    "incomplete closing of the systemic artery",
                    "mesoderm-derived structure morphology in the heart phenotype",
                    "incomplete closing of the mesoderm-derived structure",
                    "increased size of the neural crest-derived structure",
                    "coronary vessel morphology phenotype",
                    "organ component layer physiology phenotype",
                    "vasculature of organ phenotype",
                    "thoracic segment blood vessel",
                    "incomplete closing of the thoracic segment blood vessel",
                    "spermatogenesis phenotype",
                    "Patent ductus arteriosus",
                    "incomplete closing of the artery",
                    "trunk blood vessel",
                    "skin of eyelid",
                    "heart blood vessel",
                    "male gamete",
                    "posterior nasal aperture morphology phenotype",
                    "incomplete closing of the heart blood vessel",
                    "sensory perception of sound",
                    "Abnormality of movement",
                    "vasculature of trunk phenotype",
                    "decreased pigmentation in multicellular organism",
                    "internal naris phenotype",
                    "Congenital malformation of the great arteries",
                    "vasculature of trunk",
                    "ductus arteriosus morphology phenotype",
                    "conceptus",
                    "reproductive process phenotype",
                    "anterior lateral plate mesoderm",
                    "semi-lunar valve morphology phenotype",
                    "aortic valve morphology phenotype",
                    "outflow tract of ventricle",
                    "circulatory organ",
                    "aortic valve",
                    "multicellular organismal reproductive process phenotype",
                    "heart morphology phenotype",
                    "Abnormal forebrain morphology",
                    "cardiogenic plate morphology phenotype",
                    "cardiac ventricle morphology phenotype",
                    "heart left ventricle morphology phenotype",
                    "herniated anatomical entity",
                    "heart tube morphology phenotype",
                    "outflow part of left ventricle morphology phenotype",
                    "manual digit 1 phalanx endochondral element",
                    "outflow tract of ventricle phenotype",
                    "outflow tract",
                    "primary heart field",
                    "cardiopharyngeal field",
                    "male reproductive organ physiology phenotype",
                    "reproductive process",
                    "cardiac chamber phenotype",
                    "heart plus pericardium",
                    "cardiac chamber",
                    "Abnormality of the uterus",
                    "Abnormal cardiac atrium morphology",
                    "valve",
                    "meso-epithelium phenotype",
                    "nervous system process phenotype",
                    "cardiac valve morphology phenotype",
                    "Hearing impairment",
                    "splanchnic layer of lateral plate mesoderm phenotype",
                    "heart tube",
                    "nose",
                    "Abnormal heart valve morphology",
                    "skin of head",
                    "primary circulatory organ",
                    "anlage",
                    "Abnormal aortic valve morphology",
                    "Abnormal heart morphology",
                    "outflow tract phenotype",
                    "increased length of the ectoderm-derived structure",
                    "left cardiac chamber phenotype",
                    "cardiac ventricle",
                    "left cardiac chamber",
                    "immune system process",
                    "heart primordium",
                    "aorta morphology phenotype",
                    "Abnormal aortic morphology",
                    "thoracic cavity blood vessel",
                    "great vessel of heart phenotype",
                    "aorta",
                    "decreased biological_process",
                    "thoracic cavity blood vessel phenotype",
                    "aorta phenotype",
                    "flat longitudinal arch of pes",
                    "increased number of organ component layer",
                    "curvature anatomical entity",
                    "Abnormal facial shape",
                    "Pes planus",
                    "decreased qualitatively system process",
                    "fused pedal digit and pedal digit",
                    "Toe syndactyly",
                    "anatomical entity morphology in the pelvic complex phenotype",
                    "fused pedal digit and anatomical entity",
                    "fused anatomical entity and pedal digit",
                    "Decreased multicellular organism mass",
                    "voluntary musculoskeletal movement",
                    "anatomical structure mass phenotype",
                    "multicellular anatomical structure mass phenotype",
                    "decreased height of the multicellular organism",
                    "decreased material anatomical entity mass",
                    "growth phenotype",
                    "Abnormality of body weight",
                    "Abnormality of skull size",
                    "multicellular organism mass phenotype",
                    "anatomical entity mass phenotype",
                    "decreased anatomical structure mass",
                    "localised male reproductive organ",
                    "Abnormal forehead morphology",
                    "head paraxial mesoderm",
                    "gray matter of forebrain",
                    "Abnormal spermatogenesis",
                    "cartilaginous neurocranium phenotype",
                    "cerebral cortex",
                    "head bone morphology phenotype",
                    "frontal cortex",
                    "Abnormal reflex",
                    "cortex of cerebral lobe",
                    "head mesenchyme phenotype",
                    "axial skeleton plus cranial skeleton",
                    "blood cell",
                    "postcranial axial skeleton",
                    "vault of skull",
                    "decreased sensory perception of mechanical stimulus",
                    "cartilaginous neurocranium",
                    "cranium",
                    "cerebral hemisphere",
                    "dermal bone phenotype",
                    "shape of frontal cortex phenotype",
                    "lens of camera-type eye",
                    "cerebral hemisphere gray matter",
                    "cranial bone phenotype",
                    "dermatocranium",
                    "pallium",
                    "head mesenchyme morphology phenotype",
                    "internal male genitalia physiology phenotype",
                    "head paraxial mesoderm morphology phenotype",
                    "head bone phenotype",
                    "uterus",
                    "cerebral cortex morphology phenotype",
                    "cranium morphology phenotype",
                    "embryonic facial prominence",
                    "head bone",
                    "neurocranium bone",
                    "lobe of cerebral hemisphere",
                    "regional part of nervous system",
                    "frontal lobe",
                    "regional part of brain",
                    "transparent eye structure phenotype",
                    "neural tube morphology phenotype",
                    "protruding anatomical entity",
                    "forehead phenotype",
                    "primary subdivision of cranial skeletal system phenotype",
                    "mandible hypoplasia",
                    "central nervous system cell part cluster",
                    "forebrain",
                    "neurocranium bone phenotype",
                    "decreased length of ectoderm-derived structure",
                    "endocrine system phenotype",
                    "neurocranium",
                    "dermal bone",
                    "bone of craniocervical region",
                    "cranial bone",
                    "intramembranous bone",
                    "membrane bone",
                    "Abnormal frontal bone morphology",
                    "tunica fibrosa of eyeball",
                    "material anatomical entity mass phenotype",
                    "Abnormal shape of the frontal region",
                    "brain gray matter phenotype",
                    "central nervous system cell part cluster phenotype",
                    "chemosensory system phenotype",
                    "gray matter of telencephalon",
                    "regional part of brain phenotype",
                    "bone of craniocervical region phenotype",
                    "central nervous system gray matter layer phenotype",
                    "frontal cortex morphology phenotype",
                    "cerebrospinal fluid morphology phenotype",
                    "internal female genitalia",
                    "cerebral cortex phenotype",
                    "epithelial tube phenotype",
                    "neural tube phenotype",
                    "prominent anatomical entity",
                    "nervous system cell part layer phenotype",
                    "forehead",
                    "Growth abnormality",
                    "gray matter of forebrain phenotype",
                    "anatomical conduit atresia",
                    "Abnormality of the anus",
                    "glans penis",
                    "dermal skeletal element phenotype",
                    "anus",
                    "increased height of the neural crest-derived structure",
                    "anatomical structure atresia",
                    "localised testis",
                    "Abnormal ear physiology",
                    "orifice",
                    "Abnormality of thrombocytes",
                    "Abnormal anus morphology",
                    "anatomical entity atresia",
                    "anus phenotype",
                    "Anal atresia",
                    "anus atresia",
                    "closing of the anatomical entity",
                    "multicellular anatomical structure atresia",
                    "closing of the anatomical structure",
                    "closing of the multicellular anatomical structure",
                    "hemopoiesis",
                    "system process",
                    "orifice phenotype",
                    "Ventriculomegaly",
                    "increased size of the organ component layer",
                    "increased size of the material anatomical entity",
                    "increased length of the non-material anatomical boundary",
                    "ventricle of nervous system phenotype",
                    "increased size of the multicellular anatomical structure",
                    "Hyperreflexia",
                    "increased size of the ectoderm-derived structure",
                    "brain ventricle/choroid plexus phenotype",
                    "material anatomical entity morphology in the heart phenotype",
                    "brain ventricle",
                    "increased size of the anatomical entity",
                    "decreased nervous system process",
                    "ventricle of nervous system",
                    "increased size of the brain ventricle/choroid plexus",
                    "incomplete closing of the roof of mouth",
                    "increased number of anatomical entity in the blood",
                    "multicellular organism development phenotype",
                    "brain",
                    "Abnormal cornea morphology",
                    "increased size of the ventricle of nervous system",
                    "obsolete cell",
                    "brain phenotype",
                    "brain ventricle/choroid plexus morphology phenotype",
                    "location of eyeball of camera-type eye phenotype",
                    "brain ventricle/choroid plexus",
                    "incomplete closing of the anatomical conduit",
                    "brain morphology phenotype",
                    "increased size of the brain ventricle",
                    "size of brain ventricle phenotype",
                    "increased size of the organ part",
                    "Atrial septal defect",
                    "Meckel diverticulum",
                    "ileum",
                    "male germ cell",
                    "Abnormal ileum morphology",
                    "hindgut phenotype",
                    "hindgut morphology phenotype",
                    "primary subdivision of skull phenotype",
                    "neural crest morphology phenotype",
                    "renal system phenotype",
                    "decreased number of anatomical structure",
                    "tube closure",
                    "zone of organ",
                    "semen",
                    "heart tube phenotype",
                    "material anatomical entity atresia",
                    "pharyngeal arch system",
                    "anatomical entity hypoplasia",
                    "neural fold phenotype",
                    "pharyngeal arch 1",
                    "Abnormality of skin pigmentation",
                    "subdivision of head phenotype",
                    "dermal skeletal element",
                    "Clinodactyly of the 5th finger",
                    "embryo development rate phenotype",
                    "gray matter",
                    "epithelium development",
                    "sclerotome morphology phenotype",
                    "subdivision of head",
                    "neurectoderm",
                    "increased number of brain ventricle in the cerebrospinal fluid",
                    "cerebral hemisphere morphology phenotype",
                    "Abnormal limb bone morphology",
                    "epithelium phenotype",
                    "ectoderm morphology phenotype",
                    "neural crest",
                    "penis",
                    "multi organ part structure phenotype",
                    "anatomical space phenotype",
                    "future nervous system",
                    "Anemia of inadequate production",
                    "male gamete generation",
                    "eyelid morphology phenotype",
                    "pharyngeal region of foregut",
                    "head morphology phenotype",
                    "autopod endochondral element phenotype",
                    "epithelial fold phenotype",
                    "Arteriovenous malformation",
                    "Lower extremity joint dislocation",
                    "Abnormal calvaria morphology",
                    "Abnormality of the face",
                    "decreased size of the palpebral fissure",
                    "pedal digit digitopodial skeleton",
                    "Abnormality of head or neck",
                    "Abnormality of eye movement",
                    "decreased length of limb endochondral element",
                    "face",
                    "craniocervical region",
                    "Abnormal blood vessel morphology",
                    "anal region",
                    "neural crest-derived structure",
                    "maxillary prominence morphology phenotype",
                    "cell development",
                    "soft palate morphology phenotype",
                    "olfactory organ",
                    "pes phenotype",
                    "gonad",
                    "lateral plate mesoderm",
                    "paired limb/fin bud phenotype",
                    "testis",
                    "cellular organisms",
                    "decreased pigmentation in skin of body",
                    "proximo-distal subdivision of respiratory tract phenotype",
                    "material anatomical entity physiology phenotype",
                    "abdominal segment bone",
                    "telencephalon",
                    "Decreased fertility",
                    "Abnormal conjugate eye movement",
                    "eye movement",
                    "reproductive system physiology phenotype",
                    "connective tissue",
                    "anatomical entity physiology phenotype",
                    "Abnormality of the outer ear",
                    "Abnormality of chromosome stability",
                    "decreased length of anatomical structure",
                    "olfactory system phenotype",
                    "Hypertrophic cardiomyopathy",
                    "heart left ventricle",
                    "Abnormal nervous system morphology",
                    "arm bone phenotype",
                    "incomplete closing of the structure with developmental contribution from neural crest",
                    "palatine uvula morphology phenotype",
                    "trachea",
                    "palatine uvula phenotype",
                    "digitopodium region",
                    "vertebra morphology phenotype",
                    "pectoral appendage bud",
                    "ulna",
                    "number of anatomical enitites of type multicellular anatomical structure phenotype",
                    "closing of the anatomical conduit",
                    "germ layer / neural crest phenotype",
                    "ectoderm-derived structure",
                    "pectoral appendage skeleton phenotype",
                    "reproductive organ",
                    "gland phenotype",
                    "Aplasia/hypoplasia of the extremities",
                    "All",
                    "ulna endochondral element",
                    "Abnormal thumb morphology",
                    "long bone morphology phenotype",
                    "decreased size of the multicellular organism",
                    "limb long bone",
                    "forelimb zeugopod",
                    "increased size of the zone of skin",
                    "Abnormality of the palpebral fissures",
                    "forelimb long bone",
                    "facial skeleton phenotype",
                    "Abnormality of the immune system",
                    "limb endochondral element phenotype",
                    "Abnormal male reproductive system physiology",
                    "forelimb bud phenotype",
                    "skeleton of limb phenotype",
                    "forelimb zeugopod skeleton",
                    "decreased sensory perception of sound",
                    "multicellular organismal movement phenotype",
                    "phalanx morphology phenotype",
                    "incomplete closing of the interatrial septum",
                    "arm bone",
                    "upper limb segment",
                    "simple eye physiology phenotype",
                    "secondary palate",
                    "duodenum phenotype",
                    "arm phenotype",
                    "zeugopod phenotype",
                    "pectoral appendage",
                    "decreased system process",
                    "incomplete closing of the septum",
                    "pectoral complex",
                    "shape of eyelid phenotype",
                    "anterior region of body",
                    "forelimb bone phenotype",
                    "pectoral appendage bud phenotype",
                    "hindlimb phenotype",
                    "arm",
                    "nerve of head region phenotype",
                    "tetrapod frontal bone",
                    "pharyngeal arch phenotype",
                    "appendage",
                    "Abnormal upper limb bone morphology",
                    "metabolic process",
                    "sexual reproduction",
                    "bone of pectoral complex phenotype",
                    "pedal digit",
                    "forelimb skeleton phenotype",
                    "Abnormality of the upper limb",
                    "neurocranium morphology phenotype",
                    "orbital region phenotype",
                    "Abnormality of the cardiovascular system",
                    "blood vessel",
                    "zone of bone organ phenotype",
                    "system process phenotype",
                    "ductus arteriosus",
                    "nervous system phenotype",
                    "circulatory system",
                    "vascular system",
                    "anatomical cavity",
                    "pelvic girdle region",
                    "Abnormality of the vasculature",
                    "Abnormal brain morphology",
                    "cardiovascular system",
                    "limb bone",
                    "eye phenotype",
                    "central nervous system gray matter layer",
                    "vasculature phenotype",
                    "artery",
                    "trunk phenotype",
                    "intromittent organ",
                    "cardiovascular system morphology phenotype",
                    "Irregular hyperpigmentation",
                    "blood vasculature",
                    "aortic system",
                    "hip joint morphology phenotype",
                    "pedal digitopodium region",
                    "anatomical entity morphology in the brain phenotype",
                    "manual digit phenotype",
                    "abdominal segment element",
                    "absent anatomical entity",
                    "mandible",
                    "cornea morphology phenotype",
                    "tetrapod frontal bone morphology phenotype",
                    "Aplasia/Hypoplasia of the testes",
                    "heart layer",
                    "Abnormal palate morphology",
                    "secondary palate morphology phenotype",
                    "postcranial axial skeletal system",
                    "increased length of the epicanthal fold",
                    "ectoderm-derived structure, curved phenotype",
                    "cardiac valve phenotype",
                    "renal system",
                    "vestibulo-auditory system phenotype",
                    "kidney phenotype",
                    "abdomen element physiology phenotype",
                    "Aplasia/Hypoplasia affecting the anterior segment of the eye",
                    "number of leukocyte phenotype",
                    "Abnormality of the urinary system",
                    "Abnormality of the upper urinary tract",
                    "subdivision of trunk",
                    "abdomen element",
                    "bone of jaw phenotype",
                    "entire embryonic mesenchyme",
                    "fused anatomical entity and anatomical entity",
                    "flat anatomical entity",
                    "Abnormal renal morphology",
                    "trunk region element",
                    "number of anatomical entities of type anatomical entity in blood phenotype",
                    "zeugopodial skeleton",
                    "kidney",
                    "oral cavity",
                    "biological_process phenotype",
                    "trunk",
                    "decreased functionality of the reproductive organ",
                    "external ectoderm morphology phenotype",
                    "Joint dislocation",
                    "foregut epithelium",
                    "immune system physiology phenotype",
                    "Eumetazoa",
                    "root",
                    "absent anatomical structure in the multicellular organism",
                    "anatomical cluster phenotype",
                    "ectoderm-derived structure phenotype",
                    "cornea, curved phenotype",
                    "integumental system",
                    "gastrula morphology phenotype",
                    "anatomical entity morphology in the skeleton of pectoral complex phenotype",
                    "epithelial fold",
                    "Abnormal morphology of the radius",
                    "heart vasculature",
                    "reproductive organ phenotype",
                    "artery morphology phenotype",
                    "Abnormality of the genitourinary system",
                    "semi-lunar valve",
                    "deviation of manual digit 5",
                    "multi-tissue structure phenotype",
                    "penis phenotype",
                    "girdle skeleton",
                    "external soft tissue zone",
                    "organ",
                    "disconnected anatomical group",
                    "roof of mouth",
                    "decreased length of arm bone",
                    "trunk mesenchyme phenotype",
                    "transudate",
                    "head",
                    "decreased size of the long bone",
                    "vein",
                    "male organism",
                    "Abnormal connection of the cardiac segments",
                    "Morphological central nervous system abnormality",
                    "Neoplasm by anatomical site",
                    "limb segment phenotype",
                    "asymmetrically curved anatomical entity",
                    "endochondral element phenotype",
                    "Abnormality of the testis size",
                    "anatomical entity mass density phenotype",
                    "Abnormal autonomic nervous system morphology",
                    "embryonic cloacal fold",
                    "increased size of the zone of organ",
                    "mandible phenotype",
                    "skeletal joint dislocation",
                    "embryonic cardiovascular system",
                    "Abnormal preputium morphology",
                    "forelimb bone",
                    "flattened anatomical entity",
                    "increased biological_process",
                    "increased number of ectoderm-derived structure in the cerebrospinal fluid",
                    "Abnormal penis morphology",
                    "renal system morphology phenotype",
                    "female reproductive organ",
                    "forelimb long bone phenotype",
                    "male reproductive system phenotype",
                    "decreased number of anatomical entity in the multicellular organism",
                    "anatomical space",
                    "eyelid",
                    "digit 5",
                    "behavior phenotype",
                    "anterior neural tube phenotype",
                    "Metazoa",
                    "anatomical structure, asymmetrically curved phenotype",
                    "neural fold",
                    "digit morphology phenotype",
                    "Eukaryota",
                    "Global developmental delay",
                    "leg",
                    "kidney morphology phenotype",
                    "Abnormal reproductive system morphology",
                    "increased qualitatively biological_process",
                    "skeleton of lower jaw",
                    "pectoral appendage skeleton",
                    "upper jaw region",
                    "individual digit of digitopodial skeleton",
                    "intromittent organ phenotype",
                    "forelimb endochondral element",
                    "bone of pectoral complex morphology phenotype",
                    "increased length of the anatomical entity",
                    "subdivision of organism along main body axis",
                    "germ layer morphology phenotype",
                    "body proper",
                    "phalanx of pes morphology phenotype",
                    "multi-tissue structure",
                    "thoracic segment organ",
                    "tetrapod frontal bone phenotype",
                    "male reproductive organ phenotype",
                    "anatomical entity morphology in the heart phenotype",
                    "Abnormal external genitalia morphology",
                    "digestive system morphology phenotype",
                    "upper urinary tract",
                    "genitourinary system",
                    "limb long bone phenotype",
                    "incomplete closing of the blood vessel",
                    "reproductive system",
                    "pelvic girdle bone/zone",
                    "protruding eyeball of camera-type eye",
                    "cardiogenic splanchnic mesoderm phenotype",
                    "respiratory system phenotype",
                    "anatomical cluster",
                    "longitudinal arch of pes",
                    "multi organ part structure",
                    "aplasia or hypoplasia of palatine uvula",
                    "female reproductive system morphology phenotype",
                    "decreased functionality of the multicellular anatomical structure",
                    "anatomical collection phenotype",
                    "phalanx of pes",
                    "hindlimb joint",
                    "Abnormal forearm bone morphology",
                    "oral cavity morphology phenotype",
                    "penis morphology phenotype",
                    "undifferentiated genital tubercle",
                    "neural groove phenotype",
                    "Abnormality of the urinary system physiology",
                    "anterior neural tube",
                    "skull phenotype",
                    "alimentary part of gastrointestinal system morphology phenotype",
                    "erythrocyte morphology phenotype",
                    "vascular system morphology phenotype",
                    "undifferentiated genital tubercle morphology phenotype",
                    "Abnormal carotid artery morphology",
                    "subdivision of organism along main body axis phenotype",
                    "digit",
                    "herniated abdominal wall",
                    "developmental process phenotype",
                    "lateral structure",
                    "large intestine morphology phenotype",
                    "erythroid lineage cell",
                    "voluntary movement behavior",
                    "limb bud morphology phenotype",
                    "formed anatomical structure",
                    "manual digit bone",
                    "urogenital fold",
                    "manus",
                    "embryonic autopod plate morphology phenotype",
                    "synovial joint of pelvic girdle",
                    "appendicular skeletal system",
                    "regional part of nervous system phenotype",
                    "blood vessel morphology phenotype",
                    "developmental process",
                    "multi-limb segment region",
                    "visual perception",
                    "structure with developmental contribution from neural crest phenotype",
                    "skeletal joint morphology phenotype",
                    "bone element",
                    "subdivision of organism along appendicular axis",
                    "Ocular anterior segment dysgenesis",
                    "decreased size of the multicellular anatomical structure",
                    "somite",
                    "external male genitalia phenotype",
                    "shape of digit phenotype",
                    "male organism phenotype",
                    "endoderm of foregut phenotype",
                    "absent anatomical entity in the multicellular organism",
                    "membrane bone phenotype",
                    "embryonic tissue morphology phenotype",
                    "incomplete closing of the secondary palate",
                    "mesenchyme",
                    "embryonic autopod plate",
                    "bone of pelvic complex morphology phenotype",
                    "multi-limb segment region phenotype",
                    "immune system morphology phenotype",
                    "biological_process",
                    "Sloping forehead",
                    "embryonic tissue phenotype",
                    "anterior chamber of eyeball",
                    "appendage girdle complex",
                    "Frontal bossing",
                    "large intestine",
                    "pedal digit bone",
                    "brain gray matter",
                    "cranial nerve",
                    "valve phenotype",
                    "decreased size of the bone of appendage girdle complex",
                    "organism subdivision",
                    "Abnormal skeletal morphology",
                    "external soft tissue zone phenotype",
                    "anatomical conduit",
                    "subdivision of trunk phenotype",
                    "palpebral fissure",
                    "hindlimb bud",
                    "oviduct",
                    "orifice atresia",
                    "Finger clinodactyly",
                    "circulatory system phenotype",
                    "Hypopigmented skin patches",
                    "organ part phenotype",
                    "decreased number of myeloid cell",
                    "asymmetrically curved cornea",
                    "visual perception phenotype",
                    "digitopodium bone phenotype",
                    "ectoderm-derived structure physiology phenotype",
                    "decreased qualitatively anatomical structure development",
                    "uvea morphology phenotype",
                    "bone element phenotype",
                    "pedal digit morphology phenotype",
                    "Abnormality of the hypothalamus-pituitary axis",
                    "main body axis",
                    "Deviation of finger",
                    "cranial skeletal system",
                    "anus morphology phenotype",
                    "germ layer phenotype",
                    "decreased size of the limb bone",
                    "craniofacial/craniocervical phenotype",
                    "digestive tract",
                    "anatomical structure formation involved in morphogenesis phenotype",
                    "Decreased head circumference",
                    "physiologic nystagmus phenotype",
                    "spinal cord phenotype",
                    "forelimb endochondral element phenotype",
                    "pelvic appendage phenotype",
                    "long bone",
                    "segment of autopod",
                    "autopod region phenotype",
                    "interatrial septum",
                    "dermal skeleton phenotype",
                    "ear phenotype",
                    "decreased size of the bone of free limb or fin",
                    "ectoderm-derived structure, asymmetrically curved phenotype",
                    "Small intestinal stenosis",
                    "autopodial extension phenotype",
                    "endochondral element",
                    "naris",
                    "reflex",
                    "pelvic complex",
                    "simple eye",
                    "hypothalamus-pituitary axis",
                    "forelimb zeugopod bone phenotype",
                    "pedal digit phalanx endochondral element",
                    "pharyngeal arch",
                    "bone of pelvic complex phenotype",
                    "ventricular system of brain",
                    "hindlimb bud morphology phenotype",
                    "reproductive system phenotype",
                    "endocrine gland phenotype",
                    "embryonic structure phenotype",
                    "outflow part of left ventricle",
                    "future central nervous system",
                    "embryo",
                    "immune system phenotype",
                    "Abnormal small intestine morphology",
                    "nose phenotype",
                    "Localized skin lesion",
                    "Abnormality of the lower limb",
                    "Cranial nerve paralysis",
                    "Abnormality of metabolism/homeostasis",
                    "upper digestive tract",
                    "subdivision of digestive tract",
                    "subdivision of tube phenotype",
                    "abdomen element phenotype",
                    "foregut morphology phenotype",
                    "great vessel of heart morphology phenotype",
                    "enteric ganglion",
                    "dermal skeleton",
                    "alimentary part of gastrointestinal system",
                    "subdivision of skeletal system",
                    "endoderm phenotype",
                    "Abnormality of the genital system",
                    "Abnormality of the musculoskeletal system",
                    "multicellular organismal reproductive process",
                    "primary heart field phenotype",
                    "manus morphology phenotype",
                    "paired limb/fin phenotype",
                    "Abnormal testis morphology",
                    "hindlimb long bone phenotype",
                    "Abnormal forearm morphology",
                    "Abnormal soft palate morphology",
                    "limb bone phenotype",
                    "system",
                    "Reduced bone mineral density",
                    "Abnormality of the amniotic fluid",
                    "digestive system",
                    "Spinal dysraphism",
                    "intermediate mesoderm morphology phenotype",
                    "blastula",
                    "Abnormal morphology of the great vessels",
                    "cranial neuron projection bundle",
                    "ureter phenotype",
                    "zone of skin morphology phenotype",
                    "duodenum morphology phenotype",
                    "eye physiology phenotype",
                    "tracheobronchial tree morphology phenotype",
                    "cavitated compound organ",
                    "arterial system",
                    "Abnormality of limbs",
                    "anatomical conduit phenotype",
                    "fused manual digit and manual digit",
                    "Opisthokonta",
                    "foregut phenotype",
                    "Abnormality of the male genitalia",
                    "Clubbing",
                    "3-D shape anatomical entity",
                    "continuant",
                    "phenotype",
                    "anucleate cell",
                    "meso-epithelium",
                    "hindlimb morphology phenotype",
                    "skeleton of pelvic complex",
                    "Abnormal male external genitalia morphology",
                    "male reproductive system morphology phenotype",
                    "Abnormal cardiovascular system morphology",
                    "digit 5 plus metapodial segment",
                    "kidney physiology phenotype",
                    "gray matter phenotype",
                    "multicellular organism",
                    "large intestine phenotype",
                    "phalanx endochondral element",
                    "Abnormality of the curvature of the cornea",
                    "skeletal system",
                    "anlage phenotype",
                    "mouth phenotype",
                    "jaw skeleton morphology phenotype",
                    "heart",
                    "Megacolon",
                    "cardiovascular system phenotype",
                    "appendicular skeleton phenotype",
                    "primary subdivision of skull",
                    "Tracheoesophageal fistula",
                    "phenotypic effect",
                    "arterial blood vessel",
                    "Azoospermia",
                    "pelvic appendage skeleton phenotype",
                    "digit phenotype",
                    "Decreased bone element mass density",
                    "hip joint phenotype",
                    "Abnormality of the respiratory system",
                    "digestive system element",
                    "protuberance",
                    "multicellular organism morphology phenotype",
                    "digestive system phenotype",
                    "organ subunit phenotype",
                    "manual digit 5",
                    "Hematological neoplasm",
                    "maxillary prominence",
                    "eukaryotic cell",
                    "germ layer",
                    "telencephalon phenotype",
                    "tube formation phenotype",
                    "alimentary part of gastrointestinal system phenotype",
                    "abdominal segment bone phenotype",
                    "limb phenotype",
                    "embryonic structure",
                    "anatomical entity",
                    "incomplete closing of the multi-tissue structure",
                    "anatomical structure",
                    "decreased biological_process in skin of body",
                    "cavitated compound organ phenotype",
                    "ocular adnexa phenotype",
                    "cardiac ventricle phenotype",
                    "pharyngeal arch morphology phenotype",
                    "malformed anatomical entity",
                    "embryo phenotype",
                    "increased size of the anatomical line",
                    "forelimb bud",
                    "forelimb",
                    "lateral structure phenotype",
                    "forelimb zeugopod bone",
                    "small intestine morphology phenotype",
                    "esophagus",
                    "Abnormality of the kidney",
                    "digitopodium bone",
                    "midface",
                    "intermediate mesoderm",
                    "heart primordium phenotype",
                    "Abnormal hip bone morphology",
                    "Abnormality of the nervous system",
                    "multicellular anatomical structure",
                    "process",
                    "multicellular anatomical structure morphology in the heart phenotype",
                    "skeleton of pedal digitopodium",
                    "occurrent",
                    "pes bone phenotype",
                    "decreased multicellular organism development",
                    "fused digit and digit",
                    "growth",
                    "Abnormality of the skin",
                    "subdivision of organism along appendicular axis phenotype",
                    "roof of mouth morphology phenotype",
                    "decreased qualitatively multicellular organismal reproductive process",
                    "systemic artery",
                    "upper urinary tract phenotype",
                    "manual digit 1 or 5",
                    "Abnormal lens morphology",
                    "migrating mesenchyme population",
                    "Abnormal digit morphology",
                    "lower limb segment phenotype",
                    "leg bone",
                    "skeletal system morphology phenotype",
                    "decreased size of the anatomical conduit",
                    "increased number of organ part",
                    "exocrine gland phenotype",
                    "multicellular anatomical structure phenotype",
                    "behavior process",
                    "Aplasia/Hypoplasia affecting the eye",
                    "incomplete closing of the organ",
                    "decreased qualitatively developmental process involved in reproduction",
                    "Abnormal large intestine morphology",
                    "skeleton of upper jaw phenotype",
                    "subdivision of digestive tract phenotype",
                    "nervous system",
                    "dorsum",
                    "cardiac septum",
                    "independent continuant",
                    "zeugopod",
                    "foregut",
                    "anatomical system phenotype",
                    "hindlimb skeleton",
                    "hepatobiliary system phenotype",
                    "anatomical system",
                    "Abnormal toe morphology",
                    "reproductive structure",
                    "artery phenotype",
                    "forelimb zeugopod morphology phenotype",
                    "ganglion",
                    "eyeball of camera-type eye",
                    "Spina bifida",
                    "anatomical system physiology phenotype",
                    "Abnormal intestine morphology",
                    "skeleton of upper jaw",
                    "delayed biological_process",
                    "acropodial skeleton",
                    "Aplasia/hypoplasia involving forearm bones",
                    "sense organ physiology phenotype",
                    "incomplete closing of the arterial blood vessel",
                    "surface structure",
                    "male reproductive organ",
                    "great vessel of heart",
                    "anatomical structure morphogenesis",
                    "intermediate mesoderm phenotype",
                    "intestine morphology phenotype",
                    "skeleton",
                    "respiratory system morphology phenotype",
                    "Umbilical hernia",
                    "presumptive structure phenotype",
                    "skeletal element phenotype",
                    "small intestine",
                    "pectoral appendage phenotype",
                    "Abnormal finger morphology",
                    "material anatomical entity phenotype",
                    "hindlimb",
                    "organ component layer",
                    "anatomical entity morphology phenotype",
                    "pelvic appendage bud",
                    "Abnormal ventriculoarterial connection",
                    "venous blood vessel",
                    "shape of continuant phenotype",
                    "mesenchyme morphology phenotype",
                    "anatomical structure phenotype",
                    "joint of girdle morphology phenotype",
                    "respiratory system",
                    "phalanx endochondral element phenotype",
                    "facial skeleton",
                    "Abnormal localization of kidney",
                    "Deviation of the hand or of fingers of the hand",
                    "limb endochondral element",
                    "paired limb/fin bud",
                    "bone of appendage girdle complex phenotype",
                    "Abnormality of the ear",
                    "decreased qualitatively sensory perception of light stimulus",
                    "pelvic region element",
                    "cell condensation",
                    "Abnormality of the digestive system",
                    "hindlimb endochondral element phenotype",
                    "limb skeleton subdivision",
                    "orbital region",
                    "Abnormal spinal cord morphology",
                    "subdivision of tube",
                    "trunk mesenchyme",
                    "incomplete closing of the multicellular anatomical structure",
                    "deviation of manual digit",
                    "appendicular skeleton",
                    "limb skeleton subdivision phenotype",
                    "increased length of the anatomical line between pupils",
                    "venous system",
                    "duodenum",
                    "reproductive system morphology phenotype",
                    "glans",
                    "cardiogenic splanchnic mesoderm",
                    "skeletal system phenotype",
                    "Abnormality of the gastrointestinal tract",
                    "pelvic appendage",
                    "genitourinary system phenotype",
                    "thoracic cavity element",
                    "ecto-epithelium",
                    "hindlimb bone phenotype",
                    "central nervous system",
                    "pedal digitopodium bone",
                    "shape of longitudinal arch of pes phenotype",
                    "Abnormal digestive system morphology",
                    "entity",
                    "immaterial anatomical entity phenotype",
                    "lateral plate mesoderm phenotype",
                    "endo-epithelium",
                    "anatomical entity phenotype",
                    "subdivision of skeleton",
                    "Short stature",
                    "tissue phenotype",
                    "material anatomical entity, curved phenotype",
                    "phalanx phenotype",
                    "prepuce of penis phenotype",
                    "nervous system physiology phenotype",
                    "pelvic appendage skeleton",
                    "anatomical line phenotype",
                    "cardiogenic splanchnic mesoderm morphology phenotype",
                    "nervous system development",
                    "Abnormality of the urethra",
                    "incomplete closing of the ductus arteriosus",
                    "posterior region of body",
                    "gamete phenotype",
                    "Abnormal long bone morphology",
                    "structure with developmental contribution from neural crest",
                    "septum phenotype",
                    "Decreased anatomical entity mass",
                    "Clubbing of toes",
                    "peripheral nervous system phenotype",
                    "anatomical projection phenotype",
                    "Abnormality of the skeletal system",
                    "Abnormal gastrointestinal tract morphology",
                    "optic cup morphology phenotype",
                    "tissue",
                    "multicellular organism phenotype",
                    "simple eye phenotype",
                    "Aplasia/Hypoplasia of the iris",
                    "mandibular prominence",
                    "digit plus metapodial segment",
                    "motile cell",
                    "long bone phenotype",
                    "autopodial extension",
                    "face morphology phenotype",
                    "exocrine gland",
                    "ecto-epithelium phenotype",
                    "neural plate phenotype",
                    "immaterial anatomical entity",
                    "pelvic appendage bud phenotype",
                    "blood cell phenotype",
                    "subdivision of skeleton phenotype",
                    "deviation of manual digit towards the middle",
                    "clavate anatomical entity",
                    "segment of pes",
                    "clavate digit",
                    "phalanx",
                    "digit 1",
                    "musculature phenotype",
                    "Abnormal atrial septum morphology",
                    "morphological feature phenotype",
                    "Abnormal appendicular skeleton morphology",
                    "pigmentation phenotype",
                    "leg phenotype",
                    "Abnormal duodenum morphology",
                    "autopod endochondral element",
                    "midface morphology phenotype",
                    "limb",
                    "Puberty and gonadal disorders",
                    "paralysed anatomical entity",
                    "umbilicus morphology phenotype",
                    "forelimb zeugopod phenotype",
                    "esophagus phenotype",
                    "trunk region element phenotype",
                    "bone of appendage girdle complex",
                    "Absent testis",
                    "mesoderm-derived structure phenotype",
                    "Decreased fertility in males",
                    "decreased size of the arm bone",
                    "shape of anatomical entity phenotype",
                    "gonad physiology phenotype",
                    "skeleton of limb",
                    "organ system subdivision phenotype",
                    "flat bone phenotype",
                    "anatomical structure physiology phenotype",
                    "paired limb/fin segment",
                    "lower limb segment",
                    "limb morphology phenotype",
                    "Abnormality of limb bone",
                    "Duodenal stenosis",
                    "decreased qualitatively biological_process",
                    "musculature of body",
                    "Cafe-au-lait spot",
                    "Limb undergrowth",
                    "developmental process involved in reproduction",
                    "musculature of body phenotype",
                    "fused manual digit and anatomical entity",
                    "hindlimb bud phenotype",
                    "skeleton phenotype",
                    "intestine",
                    "reproductive structure phenotype",
                    "Abnormal neural tube morphology",
                    "material anatomical entity",
                    "pedal digitopodium bone phenotype",
                    "decreased size of the bone of pectoral complex",
                    "decreased length of orifice",
                    "vasculature of central nervous system plus retina",
                    "pedal digit phenotype",
                    "Abnormality of reproductive system physiology",
                    "trunk region element physiology phenotype",
                    "upper limb segment phenotype",
                    "compound organ phenotype",
                    "craniocervical region phenotype",
                    "Abnormality of body height",
                    "skeleton of pes",
                    "formed ectoderm-derived structure",
                    "shape of external ear phenotype",
                    "increased number of ventricle of nervous system",
                    "involuntary movement behavior",
                    "mesenchyme phenotype",
                    "Hypospadias",
                    "manual digit 1 phalanx",
                    "hepatobiliary system",
                    "presumptive ectoderm",
                    "vasculature",
                    "hindlimb joint phenotype",
                    "decreased length of mesoderm-derived structure",
                    "dense mesenchyme tissue phenotype",
                    "erythroid lineage cell morphology phenotype",
                    "lateral plate mesoderm morphology phenotype",
                    "Abnormality iris morphology",
                    "limb bone morphology phenotype",
                    "non-material anatomical boundary phenotype",
                    "autopod bone",
                    "urethra",
                    "heart phenotype",
                    "head mesenchyme",
                    "hindlimb bone",
                    "naris phenotype",
                    "hindlimb long bone",
                    "vessel",
                    "anatomical cavity phenotype",
                    "developing mesenchymal condensation phenotype",
                    "prepuce",
                    "erythrocyte",
                    "hindlimb endochondral element",
                    "cardiogenic plate",
                    "mesoderm",
                    "neural tube",
                    "mesoderm phenotype",
                    "structure with developmental contribution from neural crest, asymmetrically curved phenotype",
                    "sensory perception",
                    "pelvic girdle skeleton",
                    "urogenital fold morphology phenotype",
                    "Phenotypic abnormality",
                    "pes bone",
                    "developing anatomical structure phenotype",
                    "abdomen",
                    "surface structure phenotype",
                    "mesoderm-derived structure",
                    "vertebra",
                    "haemolymphatic fluid",
                    "incomplete closing of the anatomical wall",
                    "paired limb/fin skeleton",
                    "cranial nerve phenotype",
                    "limb bud",
                    "Abnormal renal physiology",
                    "appendicular skeleton morphology phenotype",
                    "forelimb phenotype",
                    "external male genitalia",
                    "bone of free limb or fin phenotype",
                    "paired limb/fin skeleton phenotype",
                    "abdominal segment element phenotype",
                    "anatomical entity morphology in the appendage girdle complex phenotype",
                    "embryonic tissue",
                    "Intrauterine growth retardation",
                    "neural fold morphology phenotype",
                    "mouth",
                    "neural crest phenotype",
                    "localised organ",
                    "Abnormal oral morphology",
                    "autopod region",
                    "endochondral bone phenotype",
                    "Abnormality of the mouth",
                    "anterior chamber of eyeball morphology phenotype",
                    "vasculature of central nervous system plus retina phenotype",
                    "stylopod",
                    "aplasia or hypoplasia of anatomical entity",
                    "neural tube closure phenotype",
                    "pharyngeal arch 1 phenotype",
                    "protuberance phenotype",
                    "developing anatomical structure",
                    "jaw region",
                    "jaw skeleton",
                    "axial skeletal system",
                    "Abnormal oral cavity morphology",
                    "vertebral column",
                    "skull",
                    "cell condensation phenotype",
                    "head phenotype",
                    "olfactory system morphology phenotype",
                    "cranial skeletal system phenotype",
                    "future central nervous system phenotype",
                    "mesenchyme from somatopleure phenotype",
                    "immaterial entity",
                    "hematopoietic cell",
                    "anatomical projection",
                    "neural plate",
                    "ectoderm",
                    "Aplasia/Hypoplasia of the uvula",
                    "brain ventricle phenotype",
                    "mesoderm morphology phenotype",
                    "musculature",
                    "craniocervical region morphology phenotype",
                    "soft palate",
                    "epithelium",
                    "lower digestive tract",
                    "oral cavity phenotype",
                    "synovial joint",
                    "Abnormality of the eye",
                    "gastrula",
                    "dermatocranium phenotype",
                    "skeleton of digitopodium",
                    "pharyngeal arch 1 morphology phenotype",
                    "external anal region",
                    "musculoskeletal system phenotype",
                    "embryonic craniocervical region",
                    "platelet",
                    "irregular bone phenotype",
                    "localised reproductive organ",
                    "Abnormal uvula morphology",
                    "Renal hypoplasia/aplasia",
                    "gland",
                    "integument",
                    "cell",
                    "forelimb zeugopod bone morphology phenotype",
                    "external ear",
                    "sense organ",
                    "pelvic girdle bone/zone phenotype",
                    "non-connected functional system",
                    "vestibulo-auditory system",
                    "Abnormality of the orbital region",
                    "external genitalia phenotype",
                    "paraxial mesoderm phenotype",
                    "deviation of anatomical entity towards the middle",
                    "external ear phenotype",
                    "ear morphology phenotype",
                    "Abnormal pinna morphology",
                    "skin of body phenotype",
                    "Abnormal ear morphology",
                    "embryonic cloacal fold morphology phenotype",
                    "sensory system",
                    "endocrine system",
                    "sensory system phenotype",
                    "external ear morphology phenotype",
                    "Syndactyly",
                    "pedal digit plus metapodial segment",
                    "entire sense organ system",
                    "eye movement phenotype",
                    "limb bud phenotype",
                    "eyeball of camera-type eye phenotype",
                    "autopodial skeleton",
                    "formed organ part",
                    "Cataract",
                    "pre-chordal neural plate phenotype",
                    "anatomical wall phenotype",
                    "aplasia or hypoplasia of iris",
                    "bone of free limb or fin",
                    "camera-type eye",
                    "uvea",
                    "chordate embryonic development",
                    "aplasia or hypoplasia of uvea",
                    "primordium phenotype",
                    "bicornuate anatomical entity",
                    "formed material anatomical entity",
                    "Abnormal axial skeleton morphology",
                    "Abnormal bone ossification",
                    "sclerotome phenotype",
                    "visual system",
                    "Abnormality of globe location",
                    "increased response to stimulus",
                    "prominent forehead",
                    "digestive system element phenotype",
                    "irregular bone",
                    "unilaminar epithelium",
                    "forelimb bud morphology phenotype",
                    "decreased length of endochondral element",
                    "Abnormal joint morphology",
                    "camera-type eye morphology phenotype",
                    "aplasia or hypoplasia of eyeball of camera-type eye",
                    "sclerotome",
                    "vision/eye phenotype",
                    "male gamete generation phenotype",
                    "iris phenotype",
                    "increased number of anatomical entity in the cerebrospinal fluid",
                    "camera-type eye phenotype",
                    "Aplasia/Hypoplasia affecting the uvea",
                    "neocortex morphology phenotype",
                    "manus phenotype",
                    "serotonin secreting cell",
                    "optic vesicle",
                    "Forearm undergrowth",
                    "iris",
                    "formed multicellular anatomical structure",
                    "size of palpebral fissure phenotype",
                    "increased biological_process in skin of body",
                    "central nervous system phenotype",
                    "autonomic nervous system",
                    "eye primordium",
                    "organ component layer phenotype",
                    "anterior segment of eyeball",
                    "chamber of eyeball",
                    "skeleton of pedal acropodium",
                    "arch of centrum of vertebra phenotype",
                    "Abnormal eye morphology",
                    "heart layer morphology phenotype",
                    "decreased length of long bone",
                    "immature eye phenotype",
                    "eye primordium phenotype",
                    "drooping anatomical entity",
                    "anterior segment of eyeball morphology phenotype",
                    "Multiple cafe-au-lait spots",
                    "prepuce of penis",
                    "optic vesicle phenotype",
                    "manual digit 1 digitopodial skeleton",
                    "anatomical wall",
                    "gamete generation phenotype",
                    "organ subunit",
                    "sperm",
                    "pelvic girdle bone/zone morphology phenotype",
                    "formed organ subunit",
                    "Abnormal anterior eye segment morphology",
                    "skeleton of manual digitopodium",
                    "organism substance phenotype",
                    "arterial blood vessel phenotype",
                    "organ system subdivision",
                    "visual system phenotype",
                    "germ cell",
                    "decreased qualitatively sensory perception of sound",
                    "anterior uvea",
                    "number of anatomical enitites of type anatomical structure phenotype",
                    "digit 1 phenotype",
                    "embryo development phenotype",
                    "optic cup",
                    "unilaminar epithelium phenotype",
                    "sense organ phenotype",
                    "eye",
                    "sensory perception of light stimulus",
                    "neural plate morphology phenotype",
                    "decreased length of material anatomical entity",
                    "tube",
                    "formed chamber of eyeball",
                    "erythrocyte differentiation",
                    "compound organ",
                    "primordium",
                    "viscus",
                    "immature eye",
                    "intestine phenotype",
                    "pre-chordal neural plate",
                    "zone of organ phenotype",
                    "skin of body morphology phenotype",
                    "presumptive ectoderm phenotype",
                    "increased pigmentation",
                    "trunk bone",
                    "Hypermelanotic macule",
                    "anatomical structure development",
                    "Abnormality of the integument",
                    "zone of skin",
                    "dorsal region element phenotype",
                    "radius endochondral element",
                    "vault of skull phenotype",
                    "pigmentation",
                    "skin of body",
                    "organ phenotype",
                    "tube phenotype",
                    "integumental system phenotype",
                    "Hyperpigmentation of the skin",
                    "systemic artery phenotype",
                    "decreased qualitatively pigmentation",
                    "integument phenotype",
                    "multi cell part structure",
                    "internal naris",
                    "decreased size of the forelimb zeugopod bone",
                    "nerve of head region",
                    "Abnormal toe phalanx morphology",
                    "limb joint",
                    "Abnormal cranial nerve physiology",
                    "Weight loss",
                    "forelimb skeleton",
                    "neuron projection bundle phenotype",
                    "increased qualitatively response to stimulus",
                    "neuron projection bundle",
                    "formed anterior chamber of eyeball",
                    "cranial neuron projection bundle phenotype",
                    "Abnormal nervous system physiology",
                    "multi cell part structure phenotype",
                    "increased number of brain ventricle/choroid plexus",
                    "Abnormal skull morphology",
                    "peripheral nervous system",
                    "segment of manus",
                    "manual digit 1",
                    "lateral structure physiology phenotype",
                    "paralysed cranial nerve",
                    "Abnormality of the ureter",
                    "cranial nerve physiology phenotype",
                    "endochondral bone",
                    "nerve",
                    "nervous system morphology phenotype",
                    "nerve phenotype",
                    "aplasia or hypoplasia of skeleton",
                    "skull morphology phenotype",
                    "manual digit",
                    "lower jaw region",
                    "skeleton of manus",
                    "decreased size of the anatomical structure",
                    "Aplasia/hypoplasia involving bones of the upper limbs",
                    "anatomical entity morphology in the pectoral complex phenotype",
                    "anatomical entity morphology in the manus phenotype",
                    "brain ventricle morphology phenotype",
                    "respiratory tract",
                    "male reproductive organ morphology phenotype",
                    "small intestine phenotype",
                    "epithelial tube formation",
                    "pes morphology phenotype",
                    "forelimb morphology phenotype",
                    "Abnormality of the autonomic nervous system",
                    "Abnormal hand morphology",
                    "cranial nerve related reflex",
                    "paired limb/fin segment phenotype",
                    "aplasia or hypoplasia of manual digit",
                    "mouth morphology phenotype",
                    "pelvic region of trunk",
                    "male urethra",
                    "manual digitopodium region",
                    "increased height of the ectoderm-derived structure",
                    "decreased length of bone of free limb or fin",
                    "decreased size of the material anatomical entity",
                    "Abnormality of the hand",
                    "manual digit plus metapodial segment",
                    "fused anatomical entity and manual digit",
                    "fused anatomical entity and digit",
                    "fused digit and anatomical entity",
                    "common carotid artery plus branches morphology phenotype",
                    "systemic arterial system",
                    "increased height of the secondary palate",
                    "blood vessel phenotype",
                    "systemic artery morphology phenotype",
                    "Abnormal systemic arterial morphology",
                    "appendage girdle region",
                    "system development",
                    "Abnormality of the head",
                    "decreased length of bone of appendage girdle complex",
                    "bone element mass density phenotype",
                    "ossification",
                    "Decreased anatomical entity mass density",
                    "forehead morphology phenotype",
                    "decreased anatomical structure development",
                    "forelimb zeugopod bone hypoplasia",
                    "multicellular anatomical structure, asymmetrically curved phenotype",
                    "multicellular organismal process",
                    "face phenotype",
                    "Abnormality of bone mineral density",
                    "Abnormal bone structure",
                    "renal/urinary system phenotype",
                    "manual digit 5 plus metapodial segment",
                    "foregut epithelium phenotype",
                    "sloped anatomical entity",
                    "deviation of manual digit 5 towards the middle",
                    "musculoskeletal system",
                    "autopod bone phenotype",
                    "Deviation of the 5th finger",
                    "radius bone",
                    "digit 1 or 5",
                    "Abnormality of immune system physiology",
                    "absent gamete",
                    "abdominal segment of trunk",
                    "manual digit 5 morphology phenotype",
                    "deviation of anatomical entity",
                    "myeloid cell",
                    "limb long bone morphology phenotype",
                    "Clinodactyly",
                    "sensory perception of mechanical stimulus",
                    "external genitalia",
                    "deviation of digit towards the middle",
                    "Abnormal 5th finger morphology",
                    "decreased length of anatomical entity",
                    "organism subdivision phenotype",
                    "Short long bone",
                    "joint of girdle",
                    "aplasia or hypoplasia of ulna",
                    "vessel phenotype",
                    "skeleton of pectoral complex",
                    "appendage girdle region phenotype",
                    "Neural tube defect",
                    "decreased size of the limb endochondral element",
                    "Abnormal morphology of ulna",
                    "decreased length of forelimb endochondral element",
                    "decreased size of the material anatomical entity in the pectoral complex",
                    "epicanthal fold",
                    "autopod region morphology phenotype",
                    "decreased size of the skeletal element",
                    "concave 3-D shape anatomical entity",
                    "decreased length of multicellular anatomical structure",
                    "midface phenotype",
                    "decreased length of skeletal element",
                    "structure with developmental contribution from neural crest physiology phenotype",
                    "decreased length of endochondral bone",
                    "Upper limb undergrowth",
                    "decreased size of the forelimb endochondral element",
                    "central nervous system morphology phenotype",
                    "ventricular system of central nervous system",
                    "decreased size of the anatomical entity",
                    "limb segment",
                    "paired limb/fin",
                    "decreased size of the multicellular anatomical structure in the pectoral complex",
                    "increased size of the anatomical structure",
                    "Aplasia/Hypoplasia of the ulna",
                    "Aplasia/hypoplasia involving bones of the extremities",
                    "decreased size of the organ",
                    "cardiac atrium morphology phenotype",
                    "facial skeleton morphology phenotype",
                    "ulna phenotype",
                    "increased length of the skin of eyelid",
                    "dentary",
                    "decreased length of limb bone",
                    "decreased length of organ",
                    "palatine uvula",
                    "decreased size of the endochondral element",
                    "bone of pelvic complex",
                    "decreased length of forelimb bone",
                    "decreased length of bone element",
                    "decreased size of the anatomical entity in the pectoral complex",
                    "Abnormal choanae morphology",
                    "decreased size of the endochondral bone",
                    "urethral meatus",
                    "decreased size of the mesoderm-derived structure",
                    "primary subdivision of cranial skeletal system",
                    "prepuce of penis morphology phenotype",
                    "decreased length of bone of pectoral complex",
                    "decreased size of the anatomical structure in the pectoral complex",
                    "decreased length of forelimb zeugopod bone",
                    "incomplete closing of the arch of centrum of vertebra",
                    "anatomical entity length phenotype",
                    "forebrain phenotype",
                    "decreased size of the forelimb bone",
                    "vertebral element",
                    "reflex phenotype",
                    "incomplete closing of the vessel",
                    "phalanx of pes phenotype",
                    "appendage phenotype",
                    "ulna hypoplasia",
                    "tube development",
                    "ectoderm-derived structure atresia",
                    "decreased size of the bone element",
                    "primary circulatory organ phenotype",
                    "hemolymphoid system",
                    "transparent eye structure",
                    "epithelial tube morphogenesis",
                    "Abnormality of blood and blood-forming tissues",
                    "Neoplasm",
                    "Hip dislocation",
                    "incomplete closing of the neural crest-derived structure",
                    "incomplete closing of the coronary vessel",
                    "nervous system cell part layer",
                    "neoplasm phenotype",
                    "hematopoietic system phenotype",
                    "circulatory organ phenotype",
                    "Myelodysplasia",
                    "neurocranium phenotype",
                    "development of anatomical entity phenotype",
                    "hematopoietic system",
                    "location of anatomical entity phenotype",
                    "anatomical entity dislocation",
                    "common carotid artery plus branches",
                    "Abnormality of lower limb joint",
                    "female reproductive organ phenotype",
                    "closing of the ectoderm-derived structure",
                    "innominate bone",
                    "skeleton of manual acropodium",
                    "articular system",
                    "synovial joint of pelvic girdle morphology phenotype",
                    "decreased qualitatively reproductive process",
                    "hindlimb skeleton phenotype",
                    "Abnormal pelvic girdle bone morphology",
                    "ectoderm phenotype",
                    "respiratory tube",
                    "acropodium region",
                    "innominate bone morphology phenotype",
                    "vasculature of organ",
                    "manual digit morphology in the manus phenotype",
                    "skeletal joint phenotype",
                    "pelvic girdle skeleton phenotype",
                    "cartilaginous condensation phenotype",
                    "bone of pectoral complex",
                    "flat bone",
                    "trunk bone phenotype",
                    "hip",
                    "digestive tract epithelium phenotype",
                    "oxygen accumulating cell",
                    "articulation phenotype",
                    "skeletal element",
                    "zone of bone organ",
                    "tissue morphogenesis",
                    "articulation",
                    "Abnormal uvea morphology",
                    "girdle bone/zone",
                    "hip joint",
                    "Hypoplasia of the ulna",
                    "synovial joint phenotype",
                    "skeletal joint",
                    "indifferent external genitalia",
                    "hip dislocation",
                    "girdle skeleton phenotype",
                    "parasympathetic nervous system",
                    "anatomical collection",
                    "girdle bone/zone phenotype",
                    "Abnormal vascular morphology",
                    "pelvic region element phenotype",
                    "paraxial mesoderm",
                    "ocular surface region",
                    "Ptosis",
                    "innominate bone phenotype",
                    "morphological feature",
                    "Abnormal hip joint morphology",
                    "embryonic epithelial tube formation",
                    "endo-epithelium phenotype",
                    "localised reproductive structure",
                    "female organism phenotype",
                    "mesenchyme from somatopleure",
                    "increased size of the immaterial anatomical entity",
                    "neurectoderm phenotype",
                    "ear",
                    "bone of hip region",
                    "femur",
                    "Abnormal respiratory system morphology",
                    "Abnormal femur morphology",
                    "hindlimb stylopod",
                    "femur endochondral element",
                    "increased number of ectoderm-derived structure",
                    "musculoskeletal movement",
                    "primary neural tube formation",
                    "cardiac valve",
                    "Abnormal lower limb bone morphology",
                    "endoderm morphology phenotype",
                    "tracheobronchial tree",
                    "endoderm-derived structure phenotype",
                    "viscus phenotype",
                    "increased number of multicellular anatomical structure in the cerebrospinal fluid",
                    "thoracic segment organ phenotype",
                    "Pyridoxine-responsive sideroblastic anemia",
                    "digestive tract epithelium",
                    "Abnormal tracheobronchial morphology",
                    "paraxial mesoderm morphology phenotype",
                    "presumptive structure",
                    "endoderm of foregut",
                    "Abnormal tracheal morphology",
                    "intramembranous bone phenotype",
                    "dense mesenchyme tissue",
                    "synovial joint morphology phenotype",
                    "proximo-distal subdivision of respiratory tract",
                    "Abnormality of the abdominal organs",
                    "neocortex",
                    "Abnormal esophagus morphology",
                    "Finger syndactyly",
                    "esophagus morphology phenotype",
                    "splanchnic layer of lateral plate mesoderm",
                    "material entity",
                    "respiratory airway",
                    "endoderm-derived structure",
                    "lower respiratory tract",
                    "Aganglionic megacolon",
                    "digestive system gland",
                    "abdominal wall phenotype",
                    "Oligohydramnios",
                    "size of anatomical entity phenotype",
                    "endoderm",
                    "male reproductive system",
                    "thoracic segment of trunk",
                    "pes",
                    "neural tube development",
                    "presomitic mesoderm",
                    "external ectoderm",
                    "vertebral column phenotype",
                    "biological_process rate phenotype",
                    "dorsal region element",
                    "excretory system",
                    "Abnormal foot morphology",
                    "cartilage element",
                    "increased pigmentation in skin of body",
                    "arch of centrum of vertebra",
                    "germ layer / neural crest",
                    "embryo morphology phenotype",
                    "neural tube closure",
                    "Aplasia/hypoplasia involving bones of the hand",
                    "presomitic mesoderm morphology phenotype",
                    "neural crest-derived structure phenotype",
                    "spinal cord morphology phenotype",
                    "anatomical structure formation involved in morphogenesis",
                    "embryonic morphogenesis",
                    "tube morphogenesis",
                    "Aplasia/hypoplasia involving the skeleton",
                    "thoracic cavity element phenotype",
                    "multicellular organism development",
                    "neural tube formation",
                    "epithelial vesicle",
                    "epithelial tube",
                    "opening of the anatomical entity",
                    "gonad phenotype",
                    "taxon specific phenotype",
                    "Abnormality of the peripheral nervous system",
                    "digit 1 or 5 phenotype",
                    "tube formation",
                    "epithelial vesicle phenotype",
                    "Cardiomyopathy",
                    "incomplete closing of the skeletal element",
                    "cartilaginous condensation",
                    "embryo development",
                    "tissue development",
                    "decreased multicellular anatomical structure mass",
                    "organ part",
                    "embryo development ending in birth or egg hatching",
                    "number of anatomical enitites of type organ component layer phenotype",
                    "morphogenesis of embryonic epithelium",
                    "morphogenesis of an epithelium",
                    "subdivision of skeletal system phenotype",
                    "incomplete closing of the anatomical entity",
                    "cartilage element phenotype",
                    "presumptive paraxial mesoderm",
                    "closing of the material anatomical entity",
                    "upper leg bone",
                    "migrating mesenchyme population phenotype",
                    "increased height of the roof of mouth",
                    "incomplete closing of the anatomical structure",
                    "Decreased body weight",
                    "Aplasia/Hypoplasia of fingers",
                    "somite phenotype",
                    "Abnormal skin morphology",
                    "presomitic mesoderm phenotype",
                    "increased number of organ component layer in the cerebrospinal fluid",
                    "skin of head morphology phenotype",
                    "vertebral element phenotype",
                    "incomplete closing of the material anatomical entity",
                    "decreased qualitatively nervous system process",
                    "presumptive paraxial mesoderm phenotype",
                    "developing mesenchymal condensation",
                    "vertebral column morphology phenotype",
                    "telencephalon morphology phenotype",
                    "vertebra phenotype",
                    "tube closure phenotype",
                    "spatial pattern of anatomical entity phenotype",
                    "ganglion of peripheral nervous system",
                    "Abnormal enteric nervous system morphology",
                    "Abnormal enteric ganglion morphology",
                    "Abnormal cerebral ventricle morphology",
                    "parasympathetic ganglion",
                    "Abnormal immune system morphology",
                    "autonomic ganglion",
                    "Macule",
                    "hindgut",
                    "forebrain morphology phenotype",
                    "enteric nervous system",
                    "neural groove",
                    "spinal cord",
                    "autonomic nervous system phenotype",
                ],
                "has_phenotype_count": 106,
                "score": None,
                "exact_synonyms": [
                    "Fanconi anemia|Fanconi pancytopenia|Fanconi panmyelopathy|Fanconi's anaemia|Fanconi's anemia|Panmyelopathy, Fanconi|pancytopenia, congenital|primary erythroid hypoplasia"
                ],
                "highlighting": None,
            },
            {
                "id": "MONDO:0001083",
                "category": "biolink:Disease",
                "name": "Fanconi renotubular syndrome",
                "full_name": None,
                "deprecated": None,
                "description": "A genetic or acquired disorder characterized by impairment of the function of the proximal tubules of the kidney. It results in decreased reabsorption of electrolytes, glucose, amino acids, and other nutrients.",
                "xref": [
                    "DOID:1062",
                    "GARD:9120",
                    "MEDGEN:4653",
                    "MESH:D005198",
                    "NANDO:2100027",
                    "NANDO:2200187",
                    "NCIT:C3034",
                    "SCTID:236466005",
                    "SCTID:40488004",
                    "UMLS:C0015624",
                ],
                "provided_by": "phenio_nodes",
                "in_taxon": None,
                "in_taxon_label": None,
                "symbol": None,
                "synonym": [
                    "De toni-Fanconi syndrome",
                    "De toni-debre-Fanconi syndrome",
                    "Fanconi syndrome",
                    "Fanconi's syndrome",
                    "Fanconi-de toni syndrome",
                    "Fanconi-de-toni syndrome",
                    "Lignac-Fanconi syndrome",
                    "adult Fanconi syndrome",
                    "congenital Fanconi syndrome",
                    "deToni Fanconi syndrome",
                    "infantile nephropathic cystinosis",
                    "toni-debre-Fanconi syndrome",
                ],
                "broad_synonym": None,
                "exact_synonym": None,
                "narrow_synonym": None,
                "related_synonym": None,
                "subsets": ["gard_rare", "nord_rare", "otar", "rare"],
                "uri": None,
                "iri": None,
                "namespace": "MONDO",
                "has_phenotype": None,
                "has_phenotype_label": None,
                "has_phenotype_closure": None,
                "has_phenotype_closure_label": None,
                "has_phenotype_count": 0,
                "score": None,
                "exact_synonyms": [
                    "De toni-Fanconi syndrome|De toni-debre-Fanconi syndrome|Fanconi syndrome|Fanconi's syndrome|Fanconi-de toni syndrome|Fanconi-de-toni syndrome|Lignac-Fanconi syndrome|deToni Fanconi syndrome"
                ],
                "narrow_synonyms": ["adult Fanconi syndrome|congenital Fanconi syndrome"],
                "related_synonyms": ["infantile nephropathic cystinosis|toni-debre-Fanconi syndrome"],
                "highlighting": None,
            },
            {
                "id": "MONDO:1011504",
                "category": "biolink:Disease",
                "name": "Fanconi syndrome, horse",
                "full_name": None,
                "deprecated": None,
                "description": "Fanconi syndrome that occurs in horse.",
                "xref": ["OMIA:000366-9796"],
                "provided_by": "phenio_nodes",
                "in_taxon": None,
                "in_taxon_label": None,
                "symbol": None,
                "synonym": None,
                "broad_synonym": None,
                "exact_synonym": None,
                "narrow_synonym": None,
                "related_synonym": None,
                "subsets": None,
                "uri": None,
                "iri": None,
                "namespace": "MONDO",
                "has_phenotype": None,
                "has_phenotype_label": None,
                "has_phenotype_closure": None,
                "has_phenotype_closure_label": None,
                "has_phenotype_count": 0,
                "score": None,
                "highlighting": None,
            },
            {
                "id": "MONDO:1011502",
                "category": "biolink:Disease",
                "name": "Fanconi syndrome, cattle",
                "full_name": None,
                "deprecated": None,
                "description": "Fanconi syndrome that occurs in cattle.",
                "xref": ["OMIA:000366-9913"],
                "provided_by": "phenio_nodes",
                "in_taxon": None,
                "in_taxon_label": None,
                "symbol": None,
                "synonym": None,
                "broad_synonym": None,
                "exact_synonym": None,
                "narrow_synonym": None,
                "related_synonym": None,
                "subsets": None,
                "uri": None,
                "iri": None,
                "namespace": "MONDO",
                "has_phenotype": None,
                "has_phenotype_label": None,
                "has_phenotype_closure": None,
                "has_phenotype_closure_label": None,
                "has_phenotype_count": 0,
                "score": None,
                "highlighting": None,
            },
            {
                "id": "MONDO:0007600",
                "category": "biolink:Disease",
                "name": "primary Fanconi syndrome",
                "full_name": None,
                "deprecated": None,
                "description": "A condition in which the kidneys do not absorb certain substances into the body. These substances, such as cysteine, fructose, galactose, or glycogen, are lost in the urine. Fanconi syndrome is thought to be caused by genetic and environmental factors, and it may be diagnosed at any age. Symptoms of Fanconi syndrome include increased urine production (which may cause dehydration), weakness, and abnormalities of the bones.",
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                "provided_by": "phenio_nodes",
                "in_taxon": None,
                "in_taxon_label": None,
                "symbol": None,
                "synonym": ["FRTS1", "Fanconi renotubular syndrome 1", "primary Fanconi renotubular syndrome"],
                "broad_synonym": None,
                "exact_synonym": None,
                "narrow_synonym": None,
                "related_synonym": None,
                "subsets": ["gard_rare", "ordo_disorder", "orphanet_rare", "otar", "rare"],
                "uri": None,
                "iri": None,
                "namespace": "MONDO",
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                    "Hypophosphatemic rickets",
                    "Hypouricemia",
                    "Decreased circulating carnitine concentration",
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                    "Increased susceptibility to fractures",
                    "Bone pain",
                    "Hypophosphatemia",
                    "Weight loss",
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                    "Abnormal urine pH",
                    "Hyperchloremic metabolic acidosis",
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                    "Renal phosphate wasting",
                    "delayed growth",
                    "delayed biological_process",
                    "Growth delay",
                    "urine amino acid level phenotype",
                    "amino acid level phenotype",
                    "Generalized aminoaciduria",
                    "increased level of amino acid in urine",
                    "increased level of glucose in urine",
                    "urine glucose level phenotype",
                    "peptide",
                    "primary amide",
                    "organic amino compound",
                    "carboxamide",
                    "Proteinuria",
                    "protein polypeptide chain",
                    "polypeptide",
                    "increased level of protein polypeptide chain in urine",
                    "Hyperuricosuria",
                    "urine uric acid level phenotype",
                    "increased level of purines",
                    "Abnormality of urinary uric acid level",
                    "Abnormality of urine bicarbonate level",
                    "hydrogencarbonate level phenotype",
                    "Abnormal urinary organic compound level",
                    "calcium atom level phenotype",
                    "taxon specific phenotype",
                    "role urine level phenotype",
                    "anatomical conduit",
                    "increased level of monosaccharide in urine",
                    "Abnormality of the musculature",
                    "metal atom",
                    "increased level of calcium atom in urine",
                    "oxygen molecular entity",
                    "lower respiratory tract",
                    "independent continuant",
                    "s-block element atom",
                    "decreased functionality of the excretory tube",
                    "decreased functionality of the tissue",
                    "abdomen element phenotype",
                    "renal system physiology phenotype",
                    "Hyperchloremic acidosis",
                    "Stage 5 chronic kidney disease",
                    "decreased level of chemical entity in blood",
                    "Abnormal renal physiology",
                    "embryo phenotype",
                    "lateral structure physiology phenotype",
                    "abdominal segment element physiology phenotype",
                    "digestive system morphology phenotype",
                    "acid bodily fluid level phenotype",
                    "Abnormality of the upper urinary tract",
                    "genitourinary system",
                    "upper urinary tract",
                    "abdominal segment element phenotype",
                    "pnictogen molecular entity",
                    "epithelial vesicle",
                    "dense mesenchyme tissue",
                    "bodily fluid",
                    "multicellular anatomical structure mass phenotype",
                    "excretory system",
                    "renal/urinary system phenotype",
                    "biological_process phenotype",
                    "multicellular organism chemical entity level phenotype",
                    "aldohexose",
                    "anatomical conduit phenotype",
                    "aromatic compound",
                    "blood oxygen molecular entity level phenotype",
                    "skeletal system morphology phenotype",
                    "mesoderm-derived structure phenotype",
                    "trunk region element phenotype",
                    "thoracic segment organ",
                    "role bodily fluid level phenotype",
                    "increased level of chemical entity in tissue",
                    "bicyclic compound",
                    "mesoderm phenotype",
                    "All",
                    "occurrent",
                    "Abnormality of the genitourinary system",
                    "organochalcogen compound",
                    "glucose",
                    "role blood level phenotype",
                    "Abnormality of the kidney",
                    "anatomical entity morphology in the respiratory system phenotype",
                    "cellular process",
                    "main group molecular entity",
                    "Pain",
                    "chemical entity level phenotype",
                    "potassium atom level phenotype",
                    "abdomen element",
                    "mesoderm",
                    "renal system phenotype",
                    "carbohydrate",
                    "Abnormal urine protein level",
                    "glucose homeostasis phenotype",
                    "lung phenotype",
                    "amino-acid derivative",
                    "carbohydrates and carbohydrate derivatives",
                    "homeostatic process",
                    "organism subdivision phenotype",
                    "Abnormality of the urinary system physiology",
                    "blood nucleobase level phenotype",
                    "kidney mesenchyme",
                    "musculoskeletal system phenotype",
                    "Abnormality of metabolism/homeostasis",
                    "Abnormal circulating lipid concentration",
                    "blood carbohydrate level phenotype",
                    "mitochondrion phenotype",
                    "chalcogen molecular entity",
                    "amide",
                    "unilaminar epithelium",
                    "hemolymphoid system",
                    "lung",
                    "haemolymphatic fluid",
                    "trunk",
                    "alkali metal atom",
                    "organism substance",
                    "growth phenotype",
                    "carbon group molecular entity",
                    "decreased functionality of the epithelium",
                    "renal system",
                    "viscus phenotype",
                    "Abnormal cellular physiology",
                    "Abnormal urine pH",
                    "Glycosuria",
                    "chemical homeostasis phenotype",
                    "tissue",
                    "anatomical entity mass density phenotype",
                    "decreased multicellular anatomical structure mass",
                    "organ physiology phenotype",
                    "Abnormality of bone mineral density",
                    "lung morphology phenotype",
                    "continuant",
                    "decreased functionality of the anatomical structure",
                    "homeostatic process phenotype",
                    "body proper",
                    "multicellular anatomical structure phenotype",
                    "respiratory system phenotype",
                    "nephron epithelium",
                    "molecular entity",
                    "endo-epithelium phenotype",
                    "anatomical collection",
                    "cavitated compound organ phenotype",
                    "anatomical structure",
                    "bone element mass density phenotype",
                    "decreased functionality of the renal tubule",
                    "organ part",
                    "unilaminar epithelium phenotype",
                    "phosphoric acid derivative",
                    "endoderm-derived structure phenotype",
                    "decreased anatomical structure mass",
                    "main group element atom",
                    "urine",
                    "multicellular organism phenotype",
                    "phosphorus oxoacids and derivatives",
                    "Growth abnormality",
                    "anatomical system",
                    "organ part phenotype",
                    "carbon oxoanion",
                    "organ phenotype",
                    "quaternary nitrogen compound",
                    "multicellular organism",
                    "anatomical system physiology phenotype",
                    "monocarboxylic acid",
                    "anatomical structure physiology phenotype",
                    "hematopoietic system phenotype",
                    "Abnormality of the skeletal system",
                    "decreased functionality of the nephron epithelium",
                    "foregut",
                    "tissue phenotype",
                    "germ layer morphology phenotype",
                    "subdivision of organism along main body axis",
                    "fatty acid",
                    "material anatomical entity phenotype",
                    "p-block molecular entity",
                    "cellular anatomical structure",
                    "trunk region element",
                    "epithelial vesicle phenotype",
                    "germ layer / neural crest phenotype",
                    "Hypercalciuria",
                    "monosaccharide",
                    "epithelium",
                    "trunk phenotype",
                    "anatomical collection phenotype",
                    "monoatomic ion",
                    "anatomical entity physiology phenotype",
                    "compound organ physiology phenotype",
                    "organic heterocyclic compound",
                    "subdivision of organism along main body axis phenotype",
                    "Decreased anatomical entity mass",
                    "aldose",
                    "Abnormal bone structure",
                    "foregut epithelium phenotype",
                    "thoracic segment of trunk",
                    "Abnormality of urine homeostasis",
                    "Abnormal circulating nitrogen compound concentration",
                    "anatomical structure phenotype",
                    "blood uric acid level phenotype",
                    "germ layer / neural crest",
                    "endoderm-derived structure",
                    "amino acid",
                    "dense mesenchyme tissue phenotype",
                    "mesenchyme phenotype",
                    "Renal tubular dysfunction",
                    "decreased functionality of the anatomical conduit",
                    "respiration organ",
                    "Abnormality of the musculoskeletal system",
                    "dipolar compound",
                    "urine organic anion level phenotype",
                    "abdominal segment element",
                    "kidney physiology phenotype",
                    "respiratory tract",
                    "kidney",
                    "anatomical system phenotype",
                    "anatomical entity morphology phenotype",
                    "lipid level phenotype",
                    "Dehydration",
                    "heterocyclic compound",
                    "respiratory system morphology phenotype",
                    "blood organic molecular entity level phenotype",
                    "material anatomical entity physiology phenotype",
                    "urine sodium atom level phenotype",
                    "multicellular anatomical structure physiology phenotype",
                    "Proximal renal tubular acidosis",
                    "anatomical entity fibrosis",
                    "endoderm phenotype",
                    "kidney phenotype",
                    "decreased level of phosphate in blood",
                    "Pulmonary fibrosis",
                    "mesoderm-derived structure",
                    "hexose",
                    "main body axis",
                    "upper urinary tract phenotype",
                    "Abnormal lung morphology",
                    "multicellular organism mass phenotype",
                    "endoderm morphology phenotype",
                    "atom",
                    "digestive tract epithelium",
                    "foregut phenotype",
                    "embryo morphology phenotype",
                    "decreased level of chemical entity in tissue",
                    "molecule",
                    "hydrogencarbonate",
                    "inorganic molecular entity",
                    "blood island",
                    "cavitated compound organ physiology phenotype",
                    "skeletal element phenotype",
                    "presumptive structure phenotype",
                    "pair of lungs",
                    "Abnormal urine phosphate concentration",
                    "growth",
                    "macromolecule",
                    "abdomen",
                    "Phenotypic abnormality",
                    "polyatomic ion",
                    "proximo-distal subdivision of respiratory tract phenotype",
                    "process",
                    "multicellular anatomical structure",
                    "excretory tube physiology phenotype",
                    "organism substance phenotype",
                    "increased level of hydrogencarbonate in urine",
                    "Abnormality of the urinary system",
                    "muscle organ",
                    "epithelium phenotype",
                    "heteroarene",
                    "thoracic segment organ phenotype",
                    "anatomical entity dysfunction in independent continuant",
                    "lateral plate mesoderm phenotype",
                    "endo-epithelium",
                    "increased level of chemical entity",
                    "subdivision of digestive tract phenotype",
                    "compound organ phenotype",
                    "nephron",
                    "proximo-distal subdivision of respiratory tract",
                    "developing anatomical structure phenotype",
                    "subdivision of digestive tract",
                    "tube",
                    "haemolymphatic fluid phenotype",
                    "organ",
                    "urine calcium atom level phenotype",
                    "cavitated compound organ",
                    "blood phenotype",
                    "thoracic cavity element phenotype",
                    "lateral plate mesoderm",
                    "Abnormal urine amino acid level",
                    "Azotemia",
                    "organonitrogen compound",
                    "organ system subdivision",
                    "foregut morphology phenotype",
                    "chemical entity",
                    "organism subdivision",
                    "cyclic compound",
                    "embryonic tissue",
                    "renal tubule",
                    "endoderm of foregut",
                    "blood glucose level phenotype",
                    "decreased level of carnitine in blood",
                    "decreased level of potassium atom in blood",
                    "embryonic tissue phenotype",
                    "organooxygen compound",
                    "Weight loss",
                    "material entity",
                    "Abnormal pulmonary interstitial morphology",
                    "increased level of carboxylic acid in urine",
                    "uric acid",
                    "digestive tract epithelium phenotype",
                    "material anatomical entity",
                    "respiratory airway",
                    "embryo",
                    "compound organ",
                    "Decreased circulating carnitine concentration",
                    "alkaline earth metal atom",
                    "mitochondrion",
                    "Abnormal respiratory system morphology",
                    "decreased functionality of the anatomical entity",
                    "decreased functionality of the epithelial tube",
                    "subdivision of trunk phenotype",
                    "digestive system phenotype",
                    "multicellular organism morphology phenotype",
                    "germ layer",
                    "heteroorganic entity",
                    "tube phenotype",
                    "Hypoglycemia",
                    "lung fibrosis",
                    "Bone pain",
                    "respiration organ phenotype",
                    "subdivision of tube",
                    "Abnormal urinary electrolyte concentration",
                    "organic molecular entity",
                    "blood chemical entity level phenotype",
                    "ion",
                    "phenotype",
                    "Chronic kidney disease",
                    "Abnormality of acid-base homeostasis",
                    "Abnormality of urine calcium concentration",
                    "germ layer phenotype",
                    "blood",
                    "monovalent inorganic cation",
                    "embryonic structure phenotype",
                    "decreased level of uric acid in blood",
                    "Osteomalacia",
                    "epithelium physiology phenotype",
                    "developing anatomical structure",
                    "Abnormality of the respiratory system",
                    "endoderm",
                    "cytoplasm",
                    "blood island phenotype",
                    "primordium phenotype",
                    "metabolic process",
                    "anion",
                    "thoracic cavity element",
                    "anatomical entity phenotype",
                    "ammonium betaine",
                    "tissue chemical entity level phenotype",
                    "Abnormal circulating organic compound concentration",
                    "abdomen element physiology phenotype",
                    "Abnormal urine metabolite level",
                    "embryonic tissue morphology phenotype",
                    "lateral structure",
                    "embryonic structure",
                    "anatomical entity",
                    "mesenchyme",
                    "digestive tract",
                    "biological_process",
                    "Abnormal circulating fatty-acid concentration",
                    "blood monoatomic ion level phenotype",
                    "viscus",
                    "primordium",
                    "increased level of chemical entity in urine",
                    "Abnormal blood phosphate concentration",
                    "increased urine role level",
                    "regulation of body fluid levels phenotype",
                    "regulation of biological quality",
                    "urine chemical entity level phenotype",
                    "biological regulation",
                    "Renal insufficiency",
                    "regulation of body fluid levels",
                    "multicellular organismal process",
                    "organic anion",
                    "Abnormality of fluid regulation",
                    "biological regulation phenotype",
                    "sodium atom",
                    "Renal sodium wasting",
                    "Abnormal urine sodium concentration",
                    "cell",
                    "sodium atom level phenotype",
                    "increased level of uric acid in urine",
                    "skeletal element",
                    "cellular_component",
                    "bone element",
                    "oxoacid derivative",
                    "intracellular membrane-bounded organelle",
                    "musculoskeletal system",
                    "epithelial tube phenotype",
                    "Reduced bone mineral density",
                    "ossification",
                    "renal tubule phenotype",
                    "phosphorus molecular entity",
                    "musculature of body",
                    "blood fatty acid level phenotype",
                    "phosphorus oxoacid derivative",
                    "phosphate",
                    "genitourinary system phenotype",
                    "presumptive structure",
                    "phosphate level phenotype",
                    "Hyperchloremic metabolic acidosis",
                    "monoatomic entity",
                    "polyatomic entity",
                    "anatomical structure mass phenotype",
                    "elemental molecular entity",
                    "excreta",
                    "lipid",
                    "musculature of body phenotype",
                    "heteroatomic molecular entity",
                    "Decreased anatomical entity mass density",
                    "trunk region element physiology phenotype",
                    "blood phosphate level phenotype",
                    "Abnormal circulating metabolite concentration",
                    "skeletal system",
                    "subdivision of tube phenotype",
                    "musculature",
                    "Rickets",
                    "carnitine",
                    "Abnormal bone ossification",
                    "blood cation level phenotype",
                    "bone element phenotype",
                    "decreased level of chemical entity",
                    "decreased functionality of the kidney epithelium",
                    "phenotypic effect",
                    "Decreased bone element mass density",
                    "Hypophosphatemia",
                    "organ system subdivision phenotype",
                    "organic molecule",
                    "potassium atom",
                    "kidney mesenchyme phenotype",
                    "organic cyclic compound",
                    "Abnormality of mitochondrial metabolism",
                    "polycyclic compound",
                    "nitrogen molecular entity",
                    "organic heterobicyclic compound",
                    "imidazopyrimidine",
                    "nucleobase",
                    "musculature phenotype",
                    "increased level of chemical entity in bodily fluid",
                    "decreased role blood level",
                    "skeletal system phenotype",
                    "Hypouricemia",
                    "Abnormal circulating nucleobase concentration",
                    "increased level of chemical entity in blood",
                    "increased level of nitrogen molecular entity in blood",
                    "blood nitrogen molecular entity level phenotype",
                    "urine potassium atom level phenotype",
                    "decreased level of purines",
                    "organic aromatic compound",
                    "heterobicyclic compound",
                    "Abnormal circulating potassium concentration",
                    "heteropolycyclic compound",
                    "lateral structure phenotype",
                    "organic heteropolycyclic compound",
                    "organonitrogen heterocyclic compound",
                    "kidney epithelium",
                    "Abnormality of body weight",
                    "purines",
                    "nitrogen molecular entity level phenotype",
                    "endoderm of foregut phenotype",
                    "decreased functionality of the nephron tubule",
                    "Increased susceptibility to fractures",
                    "polyatomic anion",
                    "nephron phenotype",
                    "hydroxides",
                    "hydrogen molecular entity",
                    "blood carnitine level phenotype",
                    "blood monocarboxylic acid level phenotype",
                    "chemical homeostasis",
                    "Abnormal urine potassium concentration",
                    "organic oxo compound",
                    "oxoacid",
                    "organic acid",
                    "blood fatty acid anion level phenotype",
                    "membrane-bounded organelle",
                    "intracellular organelle",
                    "muscle structure physiology phenotype",
                    "carboxylic acid",
                    "Aminoaciduria",
                    "carbohydrate homeostasis",
                    "fatty acid anion",
                    "onium betaine",
                    "increased level of potassium atom in urine",
                    "carboxylic acid anion",
                    "amino-acid betaine",
                    "blood carboxylic acid level phenotype",
                    "organic ion",
                    "Abnormal circulating carboxylic acid concentration",
                    "increased level of organic acid in urine",
                    "organelle",
                    "Hypokalemia",
                    "Abnormal skeletal morphology",
                    "amino-acid betaine level phenotype",
                    "Muscle weakness",
                    "fatty acid level phenotype",
                    "epithelial tube physiology phenotype",
                    "decreased level of amino-acid betaine",
                    "cation",
                    "Abnormal cellular phenotype",
                    "carbonyl compound",
                    "carbon oxoacid",
                    "monocarboxylic acid anion",
                    "zwitterion",
                    "cell phenotype",
                    "Abnormal circulating carnitine concentration",
                    "cellular_component phenotype",
                    "subdivision of trunk",
                    "Abnormal circulating fatty-acid anion concentration",
                    "blood lipid level phenotype",
                    "intracellular anatomical structure",
                    "hematopoietic system",
                    "amino acid derivative level phenotype",
                    "calcium atom",
                    "decreased muscle organ strength",
                    "Abnormality of the mitochondrion",
                    "Abnormal circulating monocarboxylic acid concentration",
                    "glucose homeostasis",
                    "digestive system",
                    "obsolete cell",
                    "Increased urinary potassium",
                    "Abnormal glucose homeostasis",
                    "inorganic cation",
                    "Abnormal blood monovalent inorganic cation concentration",
                    "Low-molecular-weight proteinuria",
                    "inorganic ion",
                    "blood potassium atom level phenotype",
                    "blood monovalent inorganic cation level phenotype",
                    "Abnormal blood cation concentration",
                    "anlage",
                    "Abnormal musculoskeletal physiology",
                    "urine phosphate level phenotype",
                    "Hypophosphatemic rickets",
                    "musculoskeletal system physiology phenotype",
                    "Constitutional symptom",
                    "Decreased body weight",
                    "anlage phenotype",
                    "tube physiology phenotype",
                    "oxoanion",
                    "material anatomical entity mass phenotype",
                    "anatomical entity mass phenotype",
                    "decreased material anatomical entity mass",
                    "Decreased multicellular organism mass",
                    "muscle structure",
                    "Bicarbonaturia",
                    "oxopurine",
                    "oxide",
                    "muscle organ physiology phenotype",
                    "muscle structure phenotype",
                    "s-block molecular entity",
                    "muscle organ phenotype",
                    "bodily fluid phenotype",
                    "respiratory system",
                    "decreased anatomical entity strength",
                    "excretory tube",
                    "Abnormal muscle physiology",
                    "Acidosis",
                    "foregut epithelium",
                    "Metabolic acidosis",
                    "tissue physiology phenotype",
                    "nephron epithelium phenotype",
                    "nephron tubule phenotype",
                    "Abnormal blood ion concentration",
                    "decreased functionality of the multicellular anatomical structure",
                    "Bicarbonate-wasting renal tubular acidosis",
                    "epithelial tube",
                    "nephron tubule",
                    "entity",
                    "anatomical conduit physiology phenotype",
                    "Abnormal homeostasis",
                    "Renal tubular acidosis",
                    "decreased functionality of the material anatomical entity",
                    "Abnormal blood glucose concentration",
                    "excretory tube phenotype",
                    "kidney epithelium phenotype",
                    "uriniferous tubule",
                    "abdominal segment of trunk",
                    "decreased functionality of the tube",
                    "urine hydrogencarbonate level phenotype",
                ],
                "has_phenotype_count": 29,
                "score": None,
                "narrow_synonyms": ["FRTS1|Fanconi renotubular syndrome 1|primary Fanconi renotubular syndrome"],
                "highlighting": None,
            },
            {
                "id": "MONDO:0009217",
                "category": "biolink:Disease",
                "name": "Fanconi-like syndrome",
                "full_name": None,
                "deprecated": None,
                "description": "A syndrome characterized by pancytopenia, immune deficiency and cutaneous malignancies.",
                "xref": [
                    "DOID:0090066",
                    "MEDGEN:56237",
                    "MESH:C536855",
                    "OMIM:227850",
                    "SCTID:236469003",
                    "UMLS:C0151638",
                ],
                "provided_by": "phenio_nodes",
                "in_taxon": None,
                "in_taxon_label": None,
                "symbol": None,
                "synonym": ["Fanconi-like syndrome"],
                "broad_synonym": None,
                "exact_synonym": None,
                "narrow_synonym": None,
                "related_synonym": None,
                "subsets": None,
                "uri": None,
                "iri": None,
                "namespace": "MONDO",
                "has_phenotype": ["HP:0002754", "HP:0001876", "HP:0005939", "HP:0002783", "HP:0007606"],
                "has_phenotype_label": [
                    "Osteomyelitis",
                    "Pancytopenia",
                    "Multiple bilateral pneumothoraces",
                    "Recurrent lower respiratory tract infections",
                    "Multiple cutaneous malignancies",
                ],
                "has_phenotype_closure": [
                    "HP:0002664",
                    "UBERON:0004121",
                    "HP:0000951",
                    "UPHENO:0003811",
                    "HP:0001574",
                    "HP:0032101",
                    "HP:0002783",
                    "HP:0002719",
                    "UBERON:0011676",
                    "HP:0011793",
                    "UBERON:0001558",
                    "UPHENO:0004064",
                    "UBERON:0013702",
                    "UBERON:0009569",
                    "HP:0012252",
                    "UBERON:0013522",
                    "UBERON:0000060",
                    "UBERON:0002199",
                    "UBERON:0000064",
                    "NCBITaxon:131567",
                    "UPHENO:0081590",
                    "UPHENO:0004481",
                    "UPHENO:0002567",
                    "UPHENO:0004900",
                    "UPHENO:0002668",
                    "UPHENO:0002571",
                    "UPHENO:0004536",
                    "UBERON:0000042",
                    "UBERON:0000077",
                    "HP:0002103",
                    "UBERON:0003258",
                    "HP:0008069",
                    "UBERON:0013701",
                    "UBERON:0010316",
                    "UPHENO:0003550",
                    "UPHENO:3000003",
                    "UBERON:0000922",
                    "UBERON:0005906",
                    "UBERON:0000025",
                    "UBERON:0001005",
                    "UBERON:0003103",
                    "UBERON:0005911",
                    "UBERON:0002048",
                    "NCBITaxon:1",
                    "UPHENO:0004891",
                    "UPHENO:0004094",
                    "UPHENO:0005029",
                    "UBERON:0005178",
                    "UPHENO:0002988",
                    "UBERON:0000923",
                    "UBERON:0005423",
                    "UBERON:0010314",
                    "NCBITaxon:2759",
                    "UPHENO:0004443",
                    "UPHENO:0088123",
                    "UBERON:0005291",
                    "UPHENO:0087665",
                    "UBERON:0000170",
                    "UBERON:0000483",
                    "UBERON:0004119",
                    "UPHENO:0003163",
                    "HP:0011843",
                    "UPHENO:0001003",
                    "UPHENO:0002525",
                    "HP:0007606",
                    "BFO:0000015",
                    "CL:0000233",
                    "UBERON:0015833",
                    "UPHENO:0002994",
                    "UPHENO:0004459",
                    "UBERON:0001434",
                    "UPHENO:0002530",
                    "UBERON:0002075",
                    "UPHENO:0002816",
                    "UBERON:0003929",
                    "CL:0000255",
                    "UBERON:0001062",
                    "UBERON:0002371",
                    "UPHENO:0003432",
                    "UPHENO:0002541",
                    "HP:0002086",
                    "CL:0000232",
                    "UBERON:0000481",
                    "UPHENO:0002870",
                    "HP:0002088",
                    "HP:0005939",
                    "UPHENO:0001001",
                    "HP:0000118",
                    "UPHENO:0002574",
                    "UBERON:0000061",
                    "UBERON:0005181",
                    "UBERON:0002390",
                    "UBERON:0000383",
                    "UPHENO:0074687",
                    "BFO:0000003",
                    "UBERON:0000072",
                    "CL:0002092",
                    "UPHENO:0074624",
                    "UPHENO:0002554",
                    "UPHENO:0002559",
                    "UPHENO:0005257",
                    "UPHENO:0080377",
                    "UPHENO:0001002",
                    "UPHENO:0074681",
                    "HP:0012649",
                    "CL:0000081",
                    "CL:0000329",
                    "UPHENO:0087433",
                    "UPHENO:0080662",
                    "UBERON:0001007",
                    "UPHENO:0002949",
                    "HP:0011947",
                    "UPHENO:0083263",
                    "NCBITaxon:6072",
                    "UPHENO:0055024",
                    "UBERON:0001474",
                    "CL:0000457",
                    "NCBITaxon:33208",
                    "UBERON:0001015",
                    "UBERON:0010000",
                    "UPHENO:0002269",
                    "UBERON:0002100",
                    "UBERON:0001048",
                    "UPHENO:0049588",
                    "HP:0002754",
                    "UPHENO:0002734",
                    "UPHENO:0082875",
                    "UBERON:0004921",
                    "UBERON:0015203",
                    "UPHENO:0087662",
                    "UPHENO:0002963",
                    "UBERON:0015212",
                    "UPHENO:0005092",
                    "CL:0001035",
                    "UPHENO:0087660",
                    "HP:0002107",
                    "GO:0008150",
                    "UPHENO:0002267",
                    "BFO:0000002",
                    "UPHENO:0002731",
                    "HP:0033127",
                    "UPHENO:0076692",
                    "GO:0006952",
                    "GO:0006950",
                    "UPHENO:0049587",
                    "UPHENO:0002964",
                    "UPHENO:0005141",
                    "UPHENO:0002564",
                    "UBERON:0004765",
                    "UPHENO:0002859",
                    "UPHENO:0049584",
                    "UPHENO:0002976",
                    "UBERON:0000475",
                    "UPHENO:0002568",
                    "UPHENO:0002548",
                    "UPHENO:0074751",
                    "CL:0000225",
                    "UBERON:0000465",
                    "UBERON:0004111",
                    "UPHENO:0054970",
                    "UPHENO:0002526",
                    "UBERON:0002097",
                    "UBERON:0001004",
                    "UPHENO:0076684",
                    "HP:0000001",
                    "HP:0002715",
                    "HP:0001876",
                    "CL:0000988",
                    "UPHENO:0049585",
                    "UPHENO:0004885",
                    "HP:0010978",
                    "UPHENO:0080693",
                    "UPHENO:0002385",
                    "UBERON:0000467",
                    "UPHENO:0005110",
                    "UBERON:0034923",
                    "UBERON:0000468",
                    "UPHENO:0049586",
                    "UPHENO:0074682",
                    "UBERON:0000062",
                    "BFO:0000004",
                    "UPHENO:0002263",
                    "UBERON:0000915",
                    "UPHENO:0002635",
                    "UBERON:0002405",
                    "UPHENO:0004680",
                    "UPHENO:0002948",
                    "UPHENO:0087359",
                    "UBERON:0001041",
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                    "UPHENO:0002754",
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                    "UBERON:0006598",
                    "UPHENO:0004482",
                ],
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                    "structure with developmental contribution from neural crest",
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                    "ectoderm-derived structure phenotype",
                    "skin of body",
                    "Abnormality of the integument",
                    "ectoderm-derived structure",
                    "Neoplasm by anatomical site",
                    "Neoplasm of the skin",
                    "Unusual infection",
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                    "skin of body phenotype",
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                    "subdivision of digestive tract",
                    "Eumetazoa",
                    "proximo-distal subdivision of respiratory tract phenotype",
                    "serous membrane phenotype",
                    "mixed endoderm/mesoderm-derived structure phenotype",
                    "body proper",
                    "germ layer / neural crest phenotype",
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                    "viscus",
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                    "organ part",
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                    "Recurrent infections",
                    "digestive system morphology phenotype",
                    "tube phenotype",
                    "response to stimulus",
                    "Multiple cutaneous malignancies",
                    "occurrent",
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                    "anatomical entity phenotype",
                    "Osteomyelitis",
                    "Increased inflammatory response",
                    "material entity",
                    "organ",
                    "biological_process phenotype",
                    "Opisthokonta",
                    "trunk",
                    "multi-tissue structure phenotype",
                    "process",
                    "hematopoietic cell",
                    "blood cell",
                    "Neoplasm",
                    "developing anatomical structure phenotype",
                    "musculature",
                    "immune system",
                    "musculoskeletal system phenotype",
                    "skeletal element phenotype",
                    "musculature of body phenotype",
                    "independent continuant",
                    "increased inflammatory response in bone element",
                    "musculature phenotype",
                    "skeletal system phenotype",
                    "increased defense response in bone element",
                    "material anatomical entity phenotype",
                    "digestive system phenotype",
                    "Abnormal inflammatory response",
                    "integumental system phenotype",
                    "Phenotypic abnormality",
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                    "Abnormality of immune system physiology",
                    "organ system subdivision",
                    "increased response to stress in bone element",
                    "inflammatory response",
                    "musculoskeletal system",
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                    "subdivision of digestive tract phenotype",
                    "response to stress phenotype",
                    "anatomical structure phenotype",
                    "increased response to stimulus in bone element",
                    "multicellular organism morphology phenotype",
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                    "continuant",
                    "All",
                    "Abnormality of blood and blood-forming tissues",
                    "multicellular organism",
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                    "embryonic tissue phenotype",
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                    "immune system phenotype",
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                    "skeletal element",
                    "response to stress",
                    "foregut morphology phenotype",
                    "Abnormality of multiple cell lineages in the bone marrow",
                    "leukocyte",
                    "multicellular anatomical structure phenotype",
                    "biogenic amine secreting cell",
                    "phenotypic effect",
                    "increased biological_process in bone element",
                    "bone marrow",
                    "multicellular anatomical structure",
                    "erythroid lineage cell",
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                    "skeletal system",
                    "increased biological_process",
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                    "embryonic tissue morphology phenotype",
                    "inflammatory response phenotype",
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                    "endoderm morphology phenotype",
                    "biological_process rate phenotype",
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                    "digestive tract",
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                    "material anatomical entity physiology phenotype",
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                    "immune system physiology phenotype",
                    "endoderm-derived structure phenotype",
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                    "digestive tract epithelium phenotype",
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                    "anatomical collection",
                    "defense response phenotype",
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                    "increased qualitatively biological_process",
                    "hematopoietic system phenotype",
                    "anatomical system physiology phenotype",
                    "anatomical structure physiology phenotype",
                    "pleura phenotype",
                    "musculoskeletal system physiology phenotype",
                    "increased inflammatory response",
                    "lateral structure",
                    "mesoderm-derived structure",
                    "embryo phenotype",
                    "serotonin secreting cell",
                    "subdivision of tube phenotype",
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                    "eukaryotic cell",
                    "Abnormality of the skin",
                    "respiratory system morphology phenotype",
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                    "anatomical entity morphology phenotype",
                    "endoderm-derived structure",
                    "anatomical entity physiology phenotype",
                    "anucleate cell",
                    "bone cell",
                    "Abnormality of the respiratory system",
                    "embryo morphology phenotype",
                    "hematopoietic system",
                    "myeloid cell",
                    "platelet",
                    "motile cell",
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                    "organ system subdivision phenotype",
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                    "increased response to stimulus",
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                    "subdivision of organism along main body axis",
                    "oxygen accumulating cell",
                    "cellular organisms",
                    "pair of lungs",
                    "serous membrane",
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                    "lateral structure phenotype",
                ],
                "has_phenotype_count": 5,
                "score": None,
                "exact_synonyms": ["Fanconi-like syndrome"],
                "highlighting": None,
            },
            {
                "id": "MONDO:0060778",
                "category": "biolink:Disease",
                "name": "adult Fanconi syndrome",
                "full_name": None,
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                "in_taxon": None,
                "in_taxon_label": None,
                "symbol": None,
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                "broad_synonym": None,
                "exact_synonym": None,
                "narrow_synonym": None,
                "related_synonym": None,
                "subsets": ["gard_rare", "rare"],
                "uri": None,
                "iri": None,
                "namespace": "MONDO",
                "has_phenotype": ["HP:0003581"],
                "has_phenotype_label": ["Adult onset"],
                "has_phenotype_closure": ["HP:0000001", "HP:0003674", "HP:0012823", "HP:0003581", "HP:0031797"],
                "has_phenotype_closure_label": ["Onset", "Adult onset", "All", "Clinical modifier", "Clinical course"],
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                "score": None,
                "exact_synonyms": ["adult Fanconi syndrome|adult Fanconi's syndrome"],
                "highlighting": None,
            },
            {
                "id": "MONDO:0060779",
                "category": "biolink:Disease",
                "name": "acquired Fanconi syndrome",
                "full_name": None,
                "deprecated": None,
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                "provided_by": "phenio_nodes",
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                "in_taxon_label": None,
                "symbol": None,
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                "exact_synonym": None,
                "narrow_synonym": None,
                "related_synonym": None,
                "subsets": ["gard_rare", "otar", "rare"],
                "uri": None,
                "iri": None,
                "namespace": "MONDO",
                "has_phenotype": None,
                "has_phenotype_label": None,
                "has_phenotype_closure": None,
                "has_phenotype_closure_label": None,
                "has_phenotype_count": 0,
                "score": None,
                "exact_synonyms": ["acquired Fanconi syndrome"],
                "highlighting": None,
            },
            {
                "id": "MONDO:1011503",
                "category": "biolink:Disease",
                "name": "Fanconi syndrome, dog",
                "full_name": None,
                "deprecated": None,
                "description": "Fanconi syndrome that occurs in dog.",
                "xref": ["OMIA:000366-9615"],
                "provided_by": "phenio_nodes",
                "in_taxon": None,
                "in_taxon_label": None,
                "symbol": None,
                "synonym": None,
                "broad_synonym": None,
                "exact_synonym": None,
                "narrow_synonym": None,
                "related_synonym": None,
                "subsets": None,
                "uri": None,
                "iri": None,
                "namespace": "MONDO",
                "has_phenotype": None,
                "has_phenotype_label": None,
                "has_phenotype_closure": None,
                "has_phenotype_closure_label": None,
                "has_phenotype_count": 0,
                "score": None,
                "highlighting": None,
            },
            {
                "id": "MONDO:0014275",
                "category": "biolink:Disease",
                "name": "Fanconi renotubular syndrome 3",
                "full_name": None,
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                "xref": ["DOID:0080759", "GARD:15991", "MEDGEN:816430", "OMIM:615605", "UMLS:C3810100"],
                "provided_by": "phenio_nodes",
                "in_taxon": None,
                "in_taxon_label": None,
                "symbol": None,
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                    "EHHADH Fanconi syndrome",
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                "exact_synonym": None,
                "narrow_synonym": None,
                "related_synonym": None,
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                "uri": None,
                "iri": None,
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                "has_phenotype_label": [
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                    "UPHENO:0041258",
                    "UPHENO:0082539",
                    "HP:0011849",
                    "UPHENO:0003093",
                    "CHEBI:24995",
                    "HP:0012337",
                    "GO:0040007",
                    "UBERON:0002390",
                    "UBERON:0011216",
                    "HP:0000002",
                    "CHEBI:33661",
                    "UPHENO:0002949",
                    "UBERON:0006314",
                    "UPHENO:0000543",
                    "UBERON:0001474",
                    "CHEBI:38261",
                    "HP:0001507",
                    "UPHENO:3000004",
                    "HP:0040064",
                    "UPHENO:0003095",
                    "UBERON:0000026",
                    "UBERON:8450002",
                    "UBERON:0000978",
                    "BFO:0000002",
                    "HP:0000119",
                    "UPHENO:0049904",
                    "UPHENO:0002964",
                    "BFO:0000040",
                    "CHEBI:26082",
                    "CHEBI:26079",
                    "UPHENO:0002385",
                    "UBERON:0010363",
                    "HP:0003109",
                    "UPHENO:0003070",
                    "CHEBI:15693",
                    "UPHENO:0031220",
                    "HP:0003110",
                    "UPHENO:0084653",
                    "UPHENO:0002642",
                    "UPHENO:0002536",
                    "HP:0004348",
                    "UPHENO:0002746",
                    "HP:0012591",
                    "UPHENO:0081581",
                    "UPHENO:0082835",
                    "UPHENO:0001001",
                    "UPHENO:0002442",
                    "HP:0003330",
                    "UBERON:0002495",
                    "UPHENO:0087665",
                    "UPHENO:0002525",
                    "UBERON:0000467",
                    "UPHENO:0003432",
                    "UPHENO:0002526",
                    "HP:0033127",
                    "UBERON:0002204",
                    "UPHENO:0002816",
                    "UBERON:0034925",
                    "UPHENO:0005092",
                    "HP:0012599",
                    "UBERON:0001015",
                    "UBERON:0001434",
                    "UPHENO:0002944",
                    "HP:0002748",
                    "UBERON:0010758",
                    "UPHENO:0031123",
                    "HP:0004349",
                    "UPHENO:0087660",
                    "HP:0001942",
                    "CHEBI:33241",
                    "UPHENO:0084763",
                    "HP:0020129",
                    "UPHENO:0076727",
                    "HP:0002813",
                    "UBERON:0000174",
                    "UPHENO:0046348",
                    "UBERON:0006058",
                    "UPHENO:0004459",
                    "UPHENO:0003516",
                    "UBERON:0002113",
                    "UPHENO:0041536",
                    "UPHENO:0081544",
                    "UPHENO:0004503",
                    "UPHENO:0003799",
                    "HP:0000940",
                    "UBERON:0004288",
                    "UPHENO:0031271",
                    "UPHENO:0088123",
                    "UPHENO:0002945",
                    "UBERON:0002101",
                    "UBERON:0003081",
                    "UBERON:0005913",
                    "UPHENO:0002585",
                    "UBERON:0004708",
                    "CHEBI:32988",
                    "UBERON:0005420",
                    "CHEBI:35605",
                    "UBERON:0002103",
                    "UBERON:0004347",
                    "UBERON:0010740",
                    "UBERON:0002513",
                    "UPHENO:0002269",
                    "UBERON:0002529",
                ],
                "has_phenotype_closure_label": [
                    "macromolecule",
                    "Proteinuria",
                    "Low-molecular-weight proteinuria",
                    "polypeptide",
                    "amino acid level phenotype",
                    "carbon oxoacid",
                    "carbonyl compound",
                    "amino acid",
                    "carboxylic acid",
                    "organic oxo compound",
                    "increased level of amino acid in urine",
                    "hydrogen molecular entity",
                    "hydroxides",
                    "size of multicellular organism phenotype",
                    "decreased size of the multicellular anatomical structure",
                    "decreased size of the multicellular organism",
                    "decreased size of the anatomical entity",
                    "Short stature",
                    "decreased height of the multicellular organism",
                    "multicellular organism height phenotype",
                    "decreased height of the anatomical entity",
                    "abdominal segment of trunk",
                    "Abnormality of the kidney",
                    "cavitated compound organ",
                    "abdominal segment element",
                    "kidney physiology phenotype",
                    "Renal insufficiency",
                    "compound organ",
                    "multicellular anatomical structure physiology phenotype",
                    "lateral structure physiology phenotype",
                    "Abnormal urine amino acid level",
                    "kidney phenotype",
                    "abdominal segment element physiology phenotype",
                    "compound organ phenotype",
                    "trunk region element physiology phenotype",
                    "cavitated compound organ physiology phenotype",
                    "Abnormality of the upper urinary tract",
                    "body proper",
                    "subdivision of trunk",
                    "abdomen element",
                    "subdivision of organism along main body axis",
                    "trunk region element",
                    "kidney",
                    "subdivision of organism along main body axis phenotype",
                    "glucose",
                    "hexose",
                    "monosaccharide",
                    "Glycosuria",
                    "Abnormal urinary organic compound level",
                    "role urine level phenotype",
                    "increased level of glucose in urine",
                    "decreased size of the anatomical structure",
                    "carbohydrates and carbohydrate derivatives",
                    "urine glucose level phenotype",
                    "lateral structure",
                    "lateral plate mesoderm morphology phenotype",
                    "limb bud morphology phenotype",
                    "organism subdivision, curved phenotype",
                    "multi-limb segment region",
                    "curved anatomical entity",
                    "embryonic tissue morphology phenotype",
                    "anatomical entity morphology in the appendage girdle complex phenotype",
                    "germ layer morphology phenotype",
                    "appendicular skeleton morphology phenotype",
                    "hindlimb",
                    "paired limb/fin skeleton",
                    "abdomen",
                    "surface structure phenotype",
                    "appendicular skeleton",
                    "subdivision of skeleton",
                    "subdivision of skeletal system",
                    "anatomical collection",
                    "limb morphology phenotype",
                    "limb bone morphology phenotype",
                    "limb bone phenotype",
                    "Abnormal limb bone morphology",
                    "hindlimb phenotype",
                    "subdivision of organism along appendicular axis phenotype",
                    "zone of long bone",
                    "aldose",
                    "bone of appendage girdle complex phenotype",
                    "compound organ physiology phenotype",
                    "diaphysis",
                    "lower limb segment",
                    "limb bone",
                    "s-block molecular entity",
                    "zone of organ",
                    "trunk phenotype",
                    "anatomical collection phenotype",
                    "increased urine role level",
                    "curvature anatomical entity",
                    "curved long bone",
                    "shape of anatomical entity phenotype",
                    "multicellular anatomical structure, curved phenotype",
                    "main body axis",
                    "upper urinary tract phenotype",
                    "zone of bone organ",
                    "pelvic appendage",
                    "limb",
                    "pelvic complex",
                    "bone of free limb or fin",
                    "leg phenotype",
                    "Abnormal appendicular skeleton morphology",
                    "skeleton of limb phenotype",
                    "mesenchyme morphology phenotype",
                    "increased level of organic acid in urine",
                    "pelvic appendage phenotype",
                    "abdominal segment element phenotype",
                    "posterior region of body",
                    "Bowing of the legs",
                    "limb bud phenotype",
                    "Bowing of the long bones",
                    "long bone phenotype",
                    "skeleton of limb",
                    "skeletal element, curved phenotype",
                    "material anatomical entity",
                    "mesenchyme",
                    "organ phenotype",
                    "urine",
                    "Aminoaciduria",
                    "blood",
                    "continuant",
                    "germ layer",
                    "multicellular organism morphology phenotype",
                    "mesenchyme phenotype",
                    "dense mesenchyme tissue phenotype",
                    "organ",
                    "biological_process",
                    "multi-limb segment region phenotype",
                    "chemical entity level phenotype",
                    "Azotemia",
                    "hindlimb zeugopod phenotype",
                    "increased level of creatinine in blood serum",
                    "creatinine",
                    "lateral structure phenotype",
                    "homeostatic process phenotype",
                    "blood plasma chemical entity level phenotype",
                    "material anatomical entity phenotype",
                    "blood phenotype",
                    "heteromonocyclic compound",
                    "developing anatomical structure phenotype",
                    "musculature",
                    "material anatomical entity, curved phenotype",
                    "phenotype",
                    "organic molecular entity",
                    "Abnormal urinary electrolyte concentration",
                    "endochondral element",
                    "zeugopod",
                    "anatomical system phenotype",
                    "anatomical entity morphology phenotype",
                    "chemical entity",
                    "shape of long bone phenotype",
                    "Abnormality of limb bone",
                    "blood nitrogen molecular entity level phenotype",
                    "limb segment",
                    "increased level of monosaccharide in urine",
                    "occurrent",
                    "germ layer / neural crest",
                    "presumptive structure",
                    "anatomical entity phenotype",
                    "anatomical system physiology phenotype",
                    "increased level of chemical entity in blood",
                    "polyatomic entity",
                    "blood plasma",
                    "pelvic appendage bud",
                    "blood chemical entity level phenotype",
                    "zeugopod phenotype",
                    "phosphoric acid derivative",
                    "blood serum",
                    "size of anatomical entity phenotype",
                    "anatomical entity",
                    "pelvic appendage bud phenotype",
                    "subdivision of skeleton phenotype",
                    "blood island",
                    "multicellular anatomical structure",
                    "material entity",
                    "multicellular organismal process",
                    "appendage",
                    "increased blood role level",
                    "embryonic tissue",
                    "germ layer / neural crest phenotype",
                    "role bodily fluid level phenotype",
                    "increased level of chemical entity in tissue",
                    "lower limb segment phenotype",
                    "blood oxygen molecular entity level phenotype",
                    "skeletal system morphology phenotype",
                    "organonitrogen heterocyclic compound",
                    "nitrogen molecular entity",
                    "material anatomical entity physiology phenotype",
                    "mesoderm",
                    "Abnormal urine protein level",
                    "appendicular skeleton phenotype",
                    "Abnormal urine metabolite level",
                    "tissue chemical entity level phenotype",
                    "Abnormal circulating organic compound concentration",
                    "paired limb/fin",
                    "embryo",
                    "hindlimb zeugopod morphology phenotype",
                    "trunk",
                    "haemolymphatic fluid",
                    "metabolic process",
                    "tissue phenotype",
                    "mesoderm morphology phenotype",
                    "molecular entity",
                    "blood organic molecular entity level phenotype",
                    "increased bodily fluid role level",
                    "monocyclic compound",
                    "multicellular anatomical structure phenotype",
                    "tissue",
                    "diazolidine",
                    "mesoderm-derived structure",
                    "main group molecular entity",
                    "Abnormal circulating nitrogen compound concentration",
                    "appendicular skeletal system",
                    "heteroorganic entity",
                    "excreta",
                    "skeletal element",
                    "limb skeleton subdivision",
                    "hematopoietic system",
                    "Phenotypic abnormality",
                    "multicellular organism",
                    "carbohydrate",
                    "Abnormal homeostasis",
                    "anatomical structure",
                    "bone element mass density phenotype",
                    "Abnormal long bone morphology",
                    "ossification",
                    "embryonic tissue phenotype",
                    "increased level of chemical entity",
                    "decreased size of the material anatomical entity",
                    "renal system",
                    "bodily fluid phenotype",
                    "increased level of nitrogen molecular entity in blood",
                    "independent continuant",
                    "Abnormality of the urinary system physiology",
                    "lateral plate mesoderm phenotype",
                    "organic molecule",
                    "increased level of chemical entity in blood serum",
                    "developing anatomical structure",
                    "phenotypic effect",
                    "Abnormality of limbs",
                    "organism substance phenotype",
                    "organonitrogen compound",
                    "lateral plate mesoderm",
                    "Abnormal renal physiology",
                    "increased level of phosphate in urine",
                    "embryo phenotype",
                    "lactam",
                    "hindlimb bud morphology phenotype",
                    "embryonic structure phenotype",
                    "germ layer phenotype",
                    "limb phenotype",
                    "embryonic structure",
                    "increased level of creatinine in blood",
                    "limb endochondral element phenotype",
                    "cyclic amide",
                    "organism subdivision phenotype",
                    "homeostatic process",
                    "anatomical system",
                    "Abnormal bone structure",
                    "protein polypeptide chain",
                    "Abnormality of metabolism/homeostasis",
                    "Abnormality of the urinary system",
                    "increased blood serum role level",
                    "blood creatinine level phenotype",
                    "organ physiology phenotype",
                    "Abnormality of bone mineral density",
                    "long bone morphology phenotype",
                    "curved hindlimb zeugopod",
                    "Abnormality of acid-base homeostasis",
                    "subdivision of skeletal system phenotype",
                    "organism substance",
                    "growth phenotype",
                    "growth",
                    "entity",
                    "lower limb segment, curved phenotype",
                    "carboxamide",
                    "upper urinary tract",
                    "genitourinary system",
                    "limb skeleton subdivision phenotype",
                    "Rickets",
                    "hindlimb bud phenotype",
                    "skeleton phenotype",
                    "genitourinary system phenotype",
                    "process",
                    "hemolymphoid system",
                    "carbon group molecular entity",
                    "primary amide",
                    "Abnormality of the genitourinary system",
                    "organochalcogen compound",
                    "phosphate level phenotype",
                    "limb segment, curved phenotype",
                    "anatomical structure phenotype",
                    "Abnormality of urine homeostasis",
                    "organooxygen compound",
                    "Elevated circulating creatinine concentration",
                    "structure with developmental contribution from neural crest",
                    "imidazolidinone",
                    "delayed growth",
                    "bone element, curved phenotype",
                    "blood island phenotype",
                    "Abnormality of body height",
                    "paired limb/fin bud",
                    "limb endochondral element",
                    "mesoderm phenotype",
                    "subdivision of organism along appendicular axis",
                    "Abnormal circulating creatinine concentration",
                    "All",
                    "Abnormal urine phosphate concentration",
                    "organic cyclic compound",
                    "embryo morphology phenotype",
                    "molecule",
                    "paired limb/fin segment, curved phenotype",
                    "p-block molecular entity",
                    "increased level of chemical entity in bodily fluid",
                    "biological_process phenotype",
                    "excretory system",
                    "imidazolidines",
                    "phosphorus molecular entity",
                    "nitrogen molecular entity level phenotype",
                    "Acidosis",
                    "anatomical entity height phenotype",
                    "cyclic compound",
                    "organism subdivision",
                    "bodily fluid",
                    "hindlimb zeugopod",
                    "dense mesenchyme tissue",
                    "Metabolic acidosis",
                    "amide",
                    "Growth delay",
                    "increased level of carboxylic acid in urine",
                    "multicellular organism chemical entity level phenotype",
                    "delayed biological_process",
                    "limb bud",
                    "multicellular organism phenotype",
                    "phosphorus oxoacids and derivatives",
                    "heterocyclic compound",
                    "Growth abnormality",
                    "pnictogen molecular entity",
                    "renal/urinary system phenotype",
                    "peptide",
                    "zeugopod, curved phenotype",
                    "oxoacid derivative",
                    "renal system phenotype",
                    "organ system subdivision",
                    "musculoskeletal system phenotype",
                    "organic heterocyclic compound",
                    "anatomical entity physiology phenotype",
                    "urine phosphate level phenotype",
                    "abdomen element phenotype",
                    "renal system physiology phenotype",
                    "phosphate",
                    "cellular process",
                    "urine chemical entity level phenotype",
                    "organic acid",
                    "oxoacid",
                    "organ, curved phenotype",
                    "heteroatomic molecular entity",
                    "aldohexose",
                    "paired limb/fin phenotype",
                    "Abnormality of the musculoskeletal system",
                    "musculoskeletal system",
                    "bone element",
                    "presumptive structure phenotype",
                    "skeleton",
                    "oxygen molecular entity",
                    "anatomical entity mass density phenotype",
                    "skeletal system phenotype",
                    "organic amino compound",
                    "increased level of chemical entity in blood plasma",
                    "Reduced bone mineral density",
                    "hematopoietic system phenotype",
                    "Abnormality of the skeletal system",
                    "musculature phenotype",
                    "paired limb/fin segment",
                    "anatomical structure physiology phenotype",
                    "skeletal element phenotype",
                    "role blood serum level phenotype",
                    "musculature of body phenotype",
                    "Abnormal diaphysis morphology",
                    "Decreased anatomical entity mass density",
                    "increased level of protein polypeptide chain in urine",
                    "anatomical entity morphology in the pelvic complex phenotype",
                    "Hyperphosphaturia",
                    "long bone",
                    "Abnormal circulating metabolite concentration",
                    "skeletal system",
                    "organ system subdivision phenotype",
                    "musculature of body",
                    "Abnormal bone ossification",
                    "bone element phenotype",
                    "Abnormal skeletal morphology",
                    "phosphorus oxoacid derivative",
                    "endochondral element phenotype",
                    "Decreased bone element mass density",
                    "role blood level phenotype",
                    "surface structure",
                    "abdomen element physiology phenotype",
                    "paired limb/fin bud phenotype",
                    "haemolymphatic fluid phenotype",
                    "paired limb/fin segment phenotype",
                    "appendage girdle complex",
                    "taxon specific phenotype",
                    "hindlimb morphology phenotype",
                    "blood serum chemical entity level phenotype",
                    "shape of hindlimb zeugopod phenotype",
                    "urine amino acid level phenotype",
                    "paired limb/fin skeleton phenotype",
                    "chalcogen molecular entity",
                    "bone of free limb or fin phenotype",
                    "anatomical structure, curved phenotype",
                    "organ part",
                    "Abnormality of the calf",
                    "shape of continuant phenotype",
                    "endochondral bone phenotype",
                    "subdivision of trunk phenotype",
                    "hindlimb bud",
                    "organic heteromonocyclic compound",
                    "subdivision of organism along appendicular axis, curved phenotype",
                    "limb segment phenotype",
                    "system",
                    "appendage phenotype",
                    "trunk region element phenotype",
                    "mesoderm-derived structure phenotype",
                    "bone of appendage girdle complex",
                    "endochondral bone",
                    "cavitated compound organ phenotype",
                    "leg",
                    "increased level of chemical entity in urine",
                    "Abnormality of the lower limb",
                ],
                "has_phenotype_count": 11,
                "score": None,
                "exact_synonyms": [
                    "EHHADH Fanconi syndrome|Fanconi renotubular syndrome 3|Fanconi renotubular syndrome type 3|Fanconi syndrome caused by mutation in EHHADH"
                ],
                "related_synonyms": ["FRTS3"],
                "highlighting": None,
            },
            {
                "id": "MONDO:0030056",
                "category": "biolink:Disease",
                "name": "Fanconi renotubular syndrome 5",
                "full_name": None,
                "deprecated": None,
                "description": None,
                "xref": ["DOID:0080761", "GARD:16392", "MEDGEN:1711127", "OMIM:618913", "UMLS:C5394473"],
                "provided_by": "phenio_nodes",
                "in_taxon": None,
                "in_taxon_label": None,
                "symbol": None,
                "synonym": [
                    "FANCONI RENOTUBULAR SYNDROME 5",
                    "FRTS5",
                    "Fanconi Renotubular Syndrome, Acadian Variant",
                    "Fanconi renotubular syndrome 5",
                ],
                "broad_synonym": None,
                "exact_synonym": None,
                "narrow_synonym": None,
                "related_synonym": None,
                "subsets": ["gard_rare", "nord_rare", "rare"],
                "uri": None,
                "iri": None,
                "namespace": "MONDO",
                "has_phenotype": [
                    "HP:0002148",
                    "HP:0002206",
                    "HP:0004912",
                    "HP:0002857",
                    "HP:0004918",
                    "HP:0045051",
                    "HP:0000093",
                    "HP:0003076",
                    "HP:0002097",
                    "HP:0003355",
                    "HP:0005576",
                    "HP:0003774",
                    "HP:0000822",
                    "HP:0030078",
                ],
                "has_phenotype_label": [
                    "Hypophosphatemia",
                    "Pulmonary fibrosis",
                    "Hypophosphatemic rickets",
                    "Genu valgum",
                    "Hyperchloremic metabolic acidosis",
                    "Decreased DLCO",
                    "Proteinuria",
                    "Glycosuria",
                    "Emphysema",
                    "Aminoaciduria",
                    "Tubulointerstitial fibrosis",
                    "Stage 5 chronic kidney disease",
                    "Hypertension",
                    "Lung adenocarcinoma",
                ],
                "has_phenotype_closure": [
                    "HP:0030358",
                    "UPHENO:3000003",
                    "UBERON:0002049",
                    "UPHENO:0004507",
                    "HP:0000822",
                    "UBERON:0000055",
                    "UBERON:0001009",
                    "UBERON:0000477",
                    "UPHENO:0002406",
                    "UPHENO:9002003",
                    "UPHENO:0002377",
                    "HP:0012622",
                    "UPHENO:0002386",
                    "UPHENO:0002360",
                    "UPHENO:0002426",
                    "UPHENO:0002422",
                    "UPHENO:0002411",
                    "HP:0000083",
                    "UBERON:0001231",
                    "UBERON:0003914",
                    "HP:0010935",
                    "UPHENO:0004791",
                    "UBERON:0007684",
                    "UPHENO:0076756",
                    "UPHENO:0076779",
                    "UPHENO:0005285",
                    "HP:0005576",
                    "UPHENO:0076714",
                    "HP:0032581",
                    "UBERON:0005172",
                    "UBERON:0011143",
                    "HP:0012210",
                    "HP:0001969",
                    "UBERON:0002417",
                    "UBERON:0007688",
                    "HP:0000091",
                    "UBERON:0006555",
                    "UBERON:0005173",
                    "UPHENO:0004969",
                    "UPHENO:0005201",
                    "CHEBI:72695",
                    "CHEBI:64709",
                    "CHEBI:36586",
                    "CHEBI:36587",
                    "CHEBI:33575",
                    "UPHENO:0068144",
                    "HP:0002097",
                    "MPATH:597",
                    "MPATH:31",
                    "HP:0011025",
                    "MPATH:0",
                    "CHEBI:17234",
                    "CHEBI:33917",
                    "CHEBI:18133",
                    "CHEBI:35381",
                    "UPHENO:0080658",
                    "HP:6000531",
                    "UPHENO:0068054",
                    "UBERON:0034923",
                    "HP:0003076",
                    "CHEBI:33304",
                    "CHEBI:15841",
                    "UBERON:0001008",
                    "CHEBI:24651",
                    "UPHENO:0068565",
                    "UPHENO:0002642",
                    "HP:0003110",
                    "HP:0000079",
                    "CHEBI:36963",
                    "CHEBI:33285",
                    "CHEBI:35352",
                    "CHEBI:33582",
                    "CHEBI:36962",
                    "CHEBI:25806",
                    "UPHENO:0002803",
                    "CHEBI:51143",
                    "CHEBI:16541",
                    "MPATH:14",
                    "UPHENO:0068110",
                    "CHEBI:16670",
                    "CHEBI:33256",
                    "UBERON:0001088",
                    "UPHENO:0002832",
                    "UPHENO:0048707",
                    "UPHENO:3000004",
                    "HP:0011277",
                    "HP:0011793",
                    "UPHENO:0002385",
                    "HP:0045051",
                    "HP:0045049",
                    "UPHENO:0068169",
                    "UPHENO:0002267",
                    "HP:0002795",
                    "HP:0004360",
                    "UPHENO:0003093",
                    "HP:0012337",
                    "HP:0001995",
                    "UBERON:0010314",
                    "UPHENO:0041591",
                    "UPHENO:0002896",
                    "UPHENO:0080300",
                    "HP:0004918",
                    "UBERON:0005055",
                    "UBERON:0003657",
                    "UBERON:8450002",
                    "UBERON:0000026",
                    "UPHENO:0002593",
                    "HP:0000093",
                    "UPHENO:0002750",
                    "UBERON:0007798",
                    "UBERON:0001981",
                    "UPHENO:0086635",
                    "UPHENO:0003411",
                    "UPHENO:0002427",
                    "UBERON:0034944",
                    "UBERON:0004905",
                    "UBERON:0034921",
                    "UPHENO:0031318",
                    "CHEBI:33839",
                    "UPHENO:0003065",
                    "UPHENO:0075945",
                    "UPHENO:0084767",
                    "UPHENO:0002885",
                    "UPHENO:0031166",
                    "UPHENO:0031122",
                    "UPHENO:0031142",
                    "HP:0011314",
                    "UPHENO:0003227",
                    "UBERON:0004769",
                    "UBERON:0003840",
                    "UBERON:0009773",
                    "UBERON:0002471",
                    "UBERON:0008784",
                    "UBERON:0002428",
                    "UBERON:0010363",
                    "UBERON:0010538",
                    "HP:0002857",
                    "UPHENO:0076740",
                    "HP:0006487",
                    "UBERON:0010912",
                    "UPHENO:0002600",
                    "HP:0025745",
                    "HP:0011844",
                    "UPHENO:0086780",
                    "CHEBI:37622",
                    "UPHENO:0002861",
                    "MPATH:25",
                    "UPHENO:0086628",
                    "RO:0002577",
                    "UBERON:0003823",
                    "UBERON:0001285",
                    "HP:0030878",
                    "UPHENO:0031323",
                    "UPHENO:0002650",
                    "UBERON:0004357",
                    "UBERON:0002091",
                    "UBERON:0004381",
                    "UBERON:0000916",
                    "HP:0002979",
                    "HP:0100491",
                    "UPHENO:0003005",
                    "UPHENO:0031302",
                    "CHEBI:33608",
                    "UPHENO:0041610",
                    "UPHENO:0088082",
                    "UPHENO:0041226",
                    "UBERON:0004819",
                    "UPHENO:0031228",
                    "CHEBI:16646",
                    "UPHENO:0002785",
                    "UPHENO:0031276",
                    "UBERON:0000075",
                    "HP:0002664",
                    "UPHENO:0002246",
                    "UPHENO:0041573",
                    "UPHENO:0004456",
                    "HP:0001941",
                    "UBERON:0015061",
                    "UBERON:0002495",
                    "UBERON:0002513",
                    "UBERON:0010740",
                    "CHEBI:35605",
                    "UBERON:0002103",
                    "UBERON:0004347",
                    "CHEBI:32988",
                    "UBERON:0005420",
                    "UPHENO:0002585",
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                    "UPHENO:0086546",
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                    "UPHENO:0003812",
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                    "UBERON:0001048",
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                    "UPHENO:0005141",
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                    "UPHENO:0005092",
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                    "HP:0020129",
                    "UPHENO:0076727",
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                    "HP:0011842",
                    "UPHENO:0002442",
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                    "UPHENO:0002525",
                    "UPHENO:0087665",
                    "UPHENO:0003432",
                    "UBERON:0002204",
                    "CHEBI:24870",
                    "UPHENO:0002816",
                    "UBERON:0001015",
                    "UBERON:0001434",
                    "UPHENO:0089294",
                    "UPHENO:0002632",
                    "HP:0004912",
                    "UPHENO:0002944",
                    "HP:0002748",
                    "UPHENO:0002754",
                    "UPHENO:0002870",
                    "UPHENO:0002559",
                    "UPHENO:0004467",
                    "UBERON:0000465",
                    "UPHENO:0003550",
                    "UPHENO:0002983",
                    "UPHENO:0049904",
                    "UPHENO:0002964",
                    "HP:0032263",
                    "UBERON:0002390",
                    "UBERON:0011216",
                    "UPHENO:0004459",
                    "UPHENO:0003516",
                    "UBERON:0002113",
                    "UPHENO:0041536",
                    "UPHENO:0068491",
                    "HP:0002981",
                    "HP:0001367",
                    "HP:0012211",
                    "CHEBI:24867",
                    "HP:0034669",
                    "UPHENO:0003095",
                    "HP:0040064",
                    "UPHENO:0031123",
                    "UBERON:0010758",
                    "UBERON:0004765",
                    "UPHENO:0003066",
                    "UPHENO:0003070",
                    "CHEBI:15693",
                    "UPHENO:0031220",
                    "UBERON:0003061",
                    "UPHENO:0002830",
                    "UPHENO:0081544",
                    "HP:0002815",
                    "UPHENO:0004503",
                    "UPHENO:0003799",
                    "HP:0000940",
                    "UPHENO:0031271",
                    "UPHENO:0002945",
                    "UBERON:0002101",
                    "UPHENO:0076767",
                    "UBERON:0003081",
                    "UBERON:0005913",
                ],
                "has_phenotype_closure_label": [
                    "Lung adenocarcinoma",
                    "Neoplasm of the respiratory system",
                    "neoplasm phenotype",
                    "Abnormality of the cardiovascular system",
                    "blood vessel",
                    "cardiovascular system",
                    "disconnected anatomical group",
                    "vessel",
                    "cardiovascular system physiology phenotype",
                    "Abnormal cardiovascular system physiology",
                    "blood vasculature",
                    "anatomical cluster",
                    "kidney physiology phenotype",
                    "Renal insufficiency",
                    "multicellular anatomical structure physiology phenotype",
                    "lateral structure physiology phenotype",
                    "trunk region element physiology phenotype",
                    "abdominal segment of trunk",
                    "Abnormal nephron morphology",
                    "cavitated compound organ",
                    "abdominal segment element",
                    "uriniferous tubule",
                    "Abnormal renal tubule morphology",
                    "nephron phenotype",
                    "kidney epithelium phenotype",
                    "Tubulointerstitial fibrosis",
                    "kidney morphology phenotype",
                    "Abnormality of the upper urinary tract",
                    "nephron morphology phenotype",
                    "abdomen element",
                    "anlage",
                    "nephron tubule",
                    "epithelial tube",
                    "kidney mesenchyme morphology phenotype",
                    "Abnormal renal insterstitial morphology",
                    "Abnormal renal morphology",
                    "kidney",
                    "amino acid level phenotype",
                    "carbon oxoacid",
                    "carbonyl compound",
                    "excretory tube phenotype",
                    "amino acid",
                    "carboxylic acid",
                    "organic oxo compound",
                    "increased level of amino acid in urine",
                    "hydrogen molecular entity",
                    "hydroxides",
                    "kidney mesenchyme phenotype",
                    "organic molecule",
                    "cell and tissue damage process",
                    "pathological phenotype observation",
                    "glucose",
                    "hexose",
                    "monosaccharide",
                    "Glycosuria",
                    "Abnormal urinary organic compound level",
                    "carbohydrates and carbohydrate derivatives",
                    "urine glucose level phenotype",
                    "circulatory system",
                    "excreta",
                    "nitrogen molecular entity level phenotype",
                    "organooxygen compound",
                    "macromolecule",
                    "increased level of chemical entity",
                    "Abnormality of the urinary system",
                    "primary amide",
                    "carboxamide",
                    "Proteinuria",
                    "Abnormality of the genitourinary system",
                    "organochalcogen compound",
                    "excretory tube",
                    "nitrogen molecular entity",
                    "upper urinary tract",
                    "genitourinary system",
                    "excretory system",
                    "renal system phenotype",
                    "polypeptide",
                    "urine",
                    "Abnormality of urine homeostasis",
                    "material anatomical entity physiology phenotype",
                    "Abnormal DLCO",
                    "Decreased DLCO",
                    "anatomical system physiology phenotype",
                    "Abnormality on pulmonary function testing",
                    "Abnormal respiratory system physiology",
                    "anatomical entity physiology phenotype",
                    "Metabolic acidosis",
                    "Acidosis",
                    "structure with developmental contribution from neural crest",
                    "lateral plate mesoderm morphology phenotype",
                    "Emphysema",
                    "limb bud morphology phenotype",
                    "organism subdivision, curved phenotype",
                    "heteroorganic entity",
                    "appendicular skeletal system",
                    "multi-limb segment region",
                    "curved anatomical entity",
                    "process of degenerative change",
                    "limb bud phenotype",
                    "anatomical entity morphology in the appendage girdle complex phenotype",
                    "appendicular skeleton morphology phenotype",
                    "hindlimb",
                    "nephron epithelium phenotype",
                    "tissue specific degenerative process",
                    "paired limb/fin skeleton",
                    "abdomen",
                    "surface structure phenotype",
                    "appendicular skeleton",
                    "subdivision of skeleton",
                    "limb morphology phenotype",
                    "Abnormal joint morphology",
                    "Chronic kidney disease",
                    "nephron tubule morphology phenotype",
                    "Abnormality of acid-base homeostasis",
                    "curved hindlimb zeugopod",
                    "limb bone phenotype",
                    "Neoplasm by anatomical site",
                    "Abnormal limb bone morphology",
                    "hindlimb phenotype",
                    "subdivision of organism along appendicular axis phenotype",
                    "zone of long bone",
                    "subdivision of skeletal system",
                    "aldose",
                    "bone of appendage girdle complex phenotype",
                    "compound organ physiology phenotype",
                    "diaphysis",
                    "abdomen element phenotype",
                    "renal system physiology phenotype",
                    "Hyperchloremic acidosis",
                    "hindlimb joint",
                    "lower limb segment",
                    "limb bone",
                    "s-block molecular entity",
                    "zone of organ",
                    "increased urine role level",
                    "curvature anatomical entity",
                    "curved long bone",
                    "shape of anatomical entity phenotype",
                    "multicellular anatomical structure, curved phenotype",
                    "pelvic appendage",
                    "limb",
                    "articulation",
                    "pelvic complex",
                    "bone of free limb or fin",
                    "leg phenotype",
                    "Abnormal appendicular skeleton morphology",
                    "skeleton of limb phenotype",
                    "mesenchyme morphology phenotype",
                    "articulation phenotype",
                    "increased level of organic acid in urine",
                    "pelvic appendage phenotype",
                    "abdominal segment element phenotype",
                    "posterior region of body",
                    "appendage",
                    "Bowing of the legs",
                    "Bowing of the long bones",
                    "long bone phenotype",
                    "skeleton of limb",
                    "skeletal element, curved phenotype",
                    "increased level of chemical entity in urine",
                    "Abnormality of the lower limb",
                    "cavitated compound organ phenotype",
                    "leg",
                    "paired limb/fin bud",
                    "limb endochondral element",
                    "Abnormality of limb bone",
                    "limb segment",
                    "long bone",
                    "endochondral bone",
                    "limb endochondral element phenotype",
                    "Neoplasm",
                    "hindlimb joint phenotype",
                    "increased level of protein polypeptide chain in urine",
                    "anatomical entity morphology in the pelvic complex phenotype",
                    "knee phenotype",
                    "Increased blood pressure",
                    "hindlimb bud morphology phenotype",
                    "digestive tract epithelium phenotype",
                    "material anatomical entity",
                    "Abnormality of the respiratory system",
                    "upper urinary tract phenotype",
                    "zone of bone organ",
                    "main body axis",
                    "thoracic segment organ phenotype",
                    "skeletal element",
                    "lateral structure phenotype",
                    "renal system",
                    "viscus phenotype",
                    "embryonic tissue morphology phenotype",
                    "Hypophosphatemic rickets",
                    "Non-small cell lung carcinoma",
                    "bone element phenotype",
                    "endoderm morphology phenotype",
                    "bodily fluid",
                    "Hypophosphatemia",
                    "pelvic appendage bud phenotype",
                    "subdivision of skeleton phenotype",
                    "blood island",
                    "genitourinary system phenotype",
                    "hindlimb bud phenotype",
                    "skeleton phenotype",
                    "process",
                    "mesenchyme",
                    "organ phenotype",
                    "limb bone morphology phenotype",
                    "endoderm of foregut",
                    "renal tubule",
                    "embryonic tissue",
                    "endoderm-derived structure phenotype",
                    "limb bud",
                    "phosphorus oxoacids and derivatives",
                    "multicellular organism phenotype",
                    "Aminoaciduria",
                    "blood",
                    "lung morphology phenotype",
                    "continuant",
                    "germ layer",
                    "multicellular organism morphology phenotype",
                    "subdivision of organism along main body axis phenotype",
                    "mesenchyme phenotype",
                    "vasculature",
                    "dense mesenchyme tissue phenotype",
                    "decreased level of chemical entity",
                    "phosphorus molecular entity",
                    "amide",
                    "respiratory airway",
                    "nephron epithelium",
                    "respiratory system phenotype",
                    "proximo-distal subdivision of respiratory tract phenotype",
                    "subdivision of organism along main body axis",
                    "tissue phenotype",
                    "organ",
                    "biological_process",
                    "multi-limb segment region phenotype",
                    "chemical entity level phenotype",
                    "pathological entity",
                    "embryonic structure phenotype",
                    "germ layer phenotype",
                    "pelvic appendage bud",
                    "knee",
                    "blood chemical entity level phenotype",
                    "epithelial vesicle phenotype",
                    "trunk region element",
                    "blood phosphate level phenotype",
                    "foregut epithelium phenotype",
                    "increased level of carboxylic acid in urine",
                    "multicellular organism chemical entity level phenotype",
                    "material anatomical entity, curved phenotype",
                    "phenotype",
                    "nephron",
                    "knee morphology phenotype",
                    "digestive tract epithelium",
                    "zeugopod",
                    "anatomical system phenotype",
                    "anatomical entity morphology phenotype",
                    "Genu valgum",
                    "respiratory system morphology phenotype",
                    "chemical entity",
                    "elemental molecular entity",
                    "shape of long bone phenotype",
                    "circulatory system phenotype",
                    "increased level of monosaccharide in urine",
                    "occurrent",
                    "anatomical structure phenotype",
                    "respiration organ",
                    "presumptive structure",
                    "anatomical entity phenotype",
                    "foregut",
                    "epithelium phenotype",
                    "urine chemical entity level phenotype",
                    "cellular process",
                    "endochondral element",
                    "biological_process phenotype",
                    "oxoacid derivative",
                    "Abnormal pulmonary interstitial morphology",
                    "subdivision of skeletal system phenotype",
                    "organism substance",
                    "multicellular anatomical structure",
                    "lateral structure",
                    "embryonic tissue phenotype",
                    "heteroatomic molecular entity",
                    "organonitrogen compound",
                    "lateral plate mesoderm",
                    "increased level of glucose in urine",
                    "foregut morphology phenotype",
                    "endochondral element phenotype",
                    "phosphorus oxoacid derivative",
                    "monoatomic entity",
                    "material anatomical entity phenotype",
                    "organ part",
                    "Abnormal blood phosphate concentration",
                    "phosphate",
                    "Abnormal renal physiology",
                    "embryo phenotype",
                    "epithelial vesicle",
                    "renal/urinary system phenotype",
                    "pnictogen molecular entity",
                    "emphysema",
                    "endo-epithelium",
                    "material entity",
                    "multicellular organismal process",
                    "primordium phenotype",
                    "phenotypic effect",
                    "developing anatomical structure",
                    "germ layer / neural crest phenotype",
                    "subdivision of trunk",
                    "embryo",
                    "hindlimb zeugopod morphology phenotype",
                    "metabolic process",
                    "Abnormality of limbs",
                    "organism substance phenotype",
                    "anatomical conduit phenotype",
                    "Hypertension",
                    "anlage phenotype",
                    "trunk",
                    "haemolymphatic fluid",
                    "molecule",
                    "embryo morphology phenotype",
                    "foregut phenotype",
                    "decreased level of chemical entity in tissue",
                    "kidney epithelium morphology phenotype",
                    "bodily fluid phenotype",
                    "organic molecular entity",
                    "ion",
                    "multicellular anatomical structure phenotype",
                    "protein polypeptide chain",
                    "Abnormality of metabolism/homeostasis",
                    "tissue",
                    "subdivision of digestive tract phenotype",
                    "compound organ phenotype",
                    "proximo-distal subdivision of respiratory tract",
                    "pathological process",
                    "anatomical entity",
                    "mesoderm morphology phenotype",
                    "molecular entity",
                    "endo-epithelium phenotype",
                    "limb phenotype",
                    "embryonic structure",
                    "lateral plate mesoderm phenotype",
                    "multicellular organism",
                    "anatomical structure",
                    "bone element mass density phenotype",
                    "renal tubule phenotype",
                    "skeletal joint",
                    "Abnormal long bone morphology",
                    "ossification",
                    "Abnormality of the urinary system physiology",
                    "independent continuant",
                    "mesoderm",
                    "Abnormal urine protein level",
                    "appendicular skeleton phenotype",
                    "Abnormal blood ion concentration",
                    "Abnormal urine metabolite level",
                    "tissue chemical entity level phenotype",
                    "skeletal joint morphology phenotype",
                    "paired limb/fin",
                    "kidney phenotype",
                    "Abnormal urine amino acid level",
                    "decreased level of phosphate in blood",
                    "endoderm phenotype",
                    "polyatomic entity",
                    "blood phenotype",
                    "thoracic cavity element phenotype",
                    "endoderm-derived structure",
                    "urine amino acid level phenotype",
                    "chalcogen molecular entity",
                    "paired limb/fin skeleton phenotype",
                    "bone of free limb or fin phenotype",
                    "anatomical structure, curved phenotype",
                    "germ layer / neural crest",
                    "nephron tubule phenotype",
                    "multi organ part structure phenotype",
                    "Hyperchloremic metabolic acidosis",
                    "limb segment, curved phenotype",
                    "phosphate level phenotype",
                    "hindlimb zeugopod phenotype",
                    "vascular system",
                    "paired limb/fin segment, curved phenotype",
                    "p-block molecular entity",
                    "abdominal segment element physiology phenotype",
                    "thoracic segment of trunk",
                    "organ part phenotype",
                    "anatomical system",
                    "Abnormal bone structure",
                    "limb skeleton subdivision",
                    "hematopoietic system",
                    "Phenotypic abnormality",
                    "Stage 5 chronic kidney disease",
                    "germ layer morphology phenotype",
                    "decreased level of chemical entity in blood",
                    "main group molecular entity",
                    "Abnormal knee morphology",
                    "hindlimb zeugopod",
                    "dense mesenchyme tissue",
                    "lower respiratory tract",
                    "developing anatomical structure phenotype",
                    "musculature",
                    "articular system",
                    "mesoderm phenotype",
                    "subdivision of organism along appendicular axis",
                    "All",
                    "foregut epithelium",
                    "homeostatic process phenotype",
                    "respiration organ phenotype",
                    "anatomical structure physiology phenotype",
                    "paired limb/fin segment",
                    "skeletal element phenotype",
                    "Abnormal tubulointerstitial morphology",
                    "organism subdivision",
                    "role urine level phenotype",
                    "anatomical conduit",
                    "thoracic cavity element",
                    "epithelium",
                    "anatomical collection phenotype",
                    "monoatomic ion",
                    "trunk phenotype",
                    "mesoderm-derived structure",
                    "Pulmonary fibrosis",
                    "body proper",
                    "Abnormality of the calf",
                    "tube phenotype",
                    "cavitated compound organ physiology phenotype",
                    "digestive system morphology phenotype",
                    "lung fibrosis",
                    "Neoplasm of the lung",
                    "carbohydrate",
                    "Abnormal homeostasis",
                    "blood monoatomic ion level phenotype",
                    "lung phenotype",
                    "organ system subdivision phenotype",
                    "musculature of body",
                    "subdivision of digestive tract",
                    "subdivision of tube",
                    "system",
                    "appendage phenotype",
                    "respiratory system physiology phenotype",
                    "Abnormal lung morphology",
                    "Abnormality of the kidney",
                    "anatomical entity morphology in the respiratory system phenotype",
                    "compound organ",
                    "Abnormal respiratory system morphology",
                    "digestive system phenotype",
                    "tube",
                    "cardiovascular system phenotype",
                    "endoderm of foregut phenotype",
                    "anatomical collection",
                    "carbon group molecular entity",
                    "unilaminar epithelium",
                    "hemolymphoid system",
                    "lung",
                    "bone element, curved phenotype",
                    "blood island phenotype",
                    "endoderm",
                    "organic acid",
                    "oxoacid",
                    "organ, curved phenotype",
                    "limb joint",
                    "zeugopod phenotype",
                    "phosphoric acid derivative",
                    "unilaminar epithelium phenotype",
                    "kidney mesenchyme",
                    "homeostatic process",
                    "organism subdivision phenotype",
                    "digestive system",
                    "kidney epithelium",
                    "respiratory system",
                    "bone of appendage girdle complex",
                    "mesoderm-derived structure phenotype",
                    "trunk region element phenotype",
                    "thoracic segment organ",
                    "viscus",
                    "respiratory tract",
                    "digestive tract",
                    "primordium",
                    "aldohexose",
                    "paired limb/fin phenotype",
                    "Abnormality of the musculoskeletal system",
                    "epithelial tube phenotype",
                    "musculoskeletal system",
                    "Renal fibrosis",
                    "bone element",
                    "presumptive structure phenotype",
                    "skeleton",
                    "lower limb segment phenotype",
                    "skeletal system morphology phenotype",
                    "oxygen molecular entity",
                    "anatomical entity mass density phenotype",
                    "skeletal system phenotype",
                    "organic amino compound",
                    "Reduced bone mineral density",
                    "organ system subdivision",
                    "musculoskeletal system phenotype",
                    "hematopoietic system phenotype",
                    "Abnormality of the skeletal system",
                    "musculature phenotype",
                    "musculature of body phenotype",
                    "Abnormal diaphysis morphology",
                    "Decreased anatomical entity mass density",
                    "Abnormal circulating metabolite concentration",
                    "skeletal system",
                    "multi organ part structure",
                    "limb skeleton subdivision phenotype",
                    "Rickets",
                    "Abnormality of the knee",
                    "Abnormal bone ossification",
                    "Abnormal skeletal morphology",
                    "Decreased bone element mass density",
                    "subdivision of tube phenotype",
                    "surface structure",
                    "Abnormality of lower limb joint",
                    "abdomen element physiology phenotype",
                    "paired limb/fin bud phenotype",
                    "haemolymphatic fluid phenotype",
                    "paired limb/fin segment phenotype",
                    "pair of lungs",
                    "entity",
                    "lower limb segment, curved phenotype",
                    "appendage girdle complex",
                    "taxon specific phenotype",
                    "hindlimb morphology phenotype",
                    "skeletal joint phenotype",
                    "anatomical entity fibrosis",
                    "shape of hindlimb zeugopod phenotype",
                    "organ physiology phenotype",
                    "renal system morphology phenotype",
                    "Abnormality of bone mineral density",
                    "long bone morphology phenotype",
                    "peptide",
                    "zeugopod, curved phenotype",
                    "shape of continuant phenotype",
                    "endochondral bone phenotype",
                    "subdivision of trunk phenotype",
                    "hindlimb bud",
                    "Abnormal systemic blood pressure",
                    "subdivision of organism along appendicular axis, curved phenotype",
                    "limb segment phenotype",
                ],
                "has_phenotype_count": 14,
                "score": None,
                "exact_synonyms": [
                    "FANCONI RENOTUBULAR SYNDROME 5|FRTS5|Fanconi Renotubular Syndrome, Acadian Variant|Fanconi renotubular syndrome 5"
                ],
                "highlighting": None,
            },
            {
                "id": "MONDO:0024525",
                "category": "biolink:Disease",
                "name": "Fanconi renotubular syndrome 1",
                "full_name": None,
                "deprecated": None,
                "description": None,
                "xref": ["DOID:0080757", "MEDGEN:1635492", "OMIM:134600", "UMLS:C4551503"],
                "provided_by": "phenio_nodes",
                "in_taxon": None,
                "in_taxon_label": None,
                "symbol": None,
                "synonym": [
                    "DeToni-Debré-Fanconi syndrome",
                    "FRTS1",
                    "Fanconi renotubular syndrome",
                    "Fanconi renotubular syndrome 1",
                    "Fanconi syndrome without cystinosis",
                    "Luder-Sheldon syndrome",
                    "adult Fanconi syndrome",
                    "primary Fanconi renal syndrome",
                    "primary Fanconi renotubular syndrome",
                    "renal Fanconi syndrome",
                ],
                "broad_synonym": None,
                "exact_synonym": None,
                "narrow_synonym": None,
                "related_synonym": None,
                "subsets": ["gard_rare", "nord_rare", "otar", "rare"],
                "uri": None,
                "iri": None,
                "namespace": "MONDO",
                "has_phenotype": [
                    "HP:0001942",
                    "HP:0002148",
                    "HP:0000124",
                    "HP:0003109",
                    "HP:0003648",
                    "HP:0002900",
                    "HP:0002749",
                    "HP:0002748",
                    "HP:0034359",
                    "HP:0003076",
                    "HP:0003155",
                    "HP:0003355",
                    "HP:0004322",
                    "HP:0003126",
                    "HP:0001324",
                    "HP:0000083",
                ],
                "has_phenotype_label": [
                    "Metabolic acidosis",
                    "Hypophosphatemia",
                    "Renal tubular dysfunction",
                    "Hyperphosphaturia",
                    "Lacticaciduria",
                    "Hypokalemia",
                    "Osteomalacia",
                    "Rickets",
                    "Impaired renal tubular reabsorption of phosphate",
                    "Glycosuria",
                    "Elevated circulating alkaline phosphatase concentration",
                    "Aminoaciduria",
                    "Short stature",
                    "Low-molecular-weight proteinuria",
                    "Muscle weakness",
                    "Renal insufficiency",
                ],
                "has_phenotype_closure": [
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                    "HP:0001324",
                    "UPHENO:0002359",
                    "HP:0003011",
                    "UPHENO:0003047",
                    "UPHENO:0002320",
                    "CHEBI:33839",
                    "HP:0000093",
                    "CHEBI:32988",
                    "CHEBI:16541",
                    "CHEBI:16670",
                    "CHEBI:33256",
                    "CHEBI:37622",
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                    "UPHENO:0069254",
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                    "CHEBI:72695",
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                    "CHEBI:36586",
                    "CHEBI:36587",
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                    "CHEBI:26216",
                    "UBERON:0011676",
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                    "UBERON:0000483",
                    "HP:0011042",
                    "UPHENO:0051635",
                    "CHEBI:36915",
                ],
                "has_phenotype_closure_label": [
                    "Renal insufficiency",
                    "Abnormal muscle physiology",
                    "muscle organ phenotype",
                    "muscle structure physiology phenotype",
                    "muscle structure phenotype",
                    "muscle organ physiology phenotype",
                    "decreased muscle organ strength",
                    "muscle structure",
                    "Abnormal urine protein level",
                    "macromolecule",
                    "primary amide",
                    "carboxamide",
                    "Proteinuria",
                    "Low-molecular-weight proteinuria",
                    "polypeptide",
                    "increased level of protein polypeptide chain in urine",
                    "Abnormality of body height",
                    "decreased size of the multicellular anatomical structure",
                    "delayed growth",
                    "decreased size of the multicellular organism",
                    "decreased size of the anatomical entity",
                    "decreased height of the multicellular organism",
                    "multicellular organism height phenotype",
                    "decreased height of the anatomical entity",
                    "amide",
                    "Growth delay",
                    "carbon oxoacid",
                    "decreased anatomical entity strength",
                    "increased level of organic acid in urine",
                    "s-block molecular entity",
                    "carboxylic acid",
                    "organic acid",
                    "oxoacid",
                    "organic oxo compound",
                    "increased level of amino acid in urine",
                    "hydrogen molecular entity",
                    "hydroxides",
                    "Abnormal circulating enzyme concentration or activity",
                    "alkaline phosphatase, tissue-nonspecific isozyme level phenotype",
                    "protein",
                    "size of multicellular organism phenotype",
                    "amino acid chain",
                    "Abnormality of alkaline phosphatase level",
                    "Abnormal enzyme concentration or activity",
                    "glucose",
                    "aldose",
                    "hexose",
                    "monosaccharide",
                    "Glycosuria",
                    "Abnormal urinary organic compound level",
                    "organooxygen compound",
                    "heteroorganic entity",
                    "increased level of glucose in urine",
                    "decreased size of the anatomical structure",
                    "carbohydrates and carbohydrate derivatives",
                    "urine glucose level phenotype",
                    "urine amino acid level phenotype",
                    "chalcogen molecular entity",
                    "renal absorption phenotype",
                    "Impaired renal tubular reabsorption of phosphate",
                    "Abnormal renal tubular resorption",
                    "renal system process phenotype",
                    "system process",
                    "system process phenotype",
                    "multicellular organismal process phenotype",
                    "Rickets",
                    "Decreased bone element mass density",
                    "Abnormal skeletal morphology",
                    "bone element phenotype",
                    "Abnormal bone ossification",
                    "musculature",
                    "multicellular organismal process",
                    "Decreased anatomical entity mass density",
                    "musculature of body phenotype",
                    "multicellular organism morphology phenotype",
                    "musculature phenotype",
                    "organic amino compound",
                    "Elevated circulating alkaline phosphatase concentration",
                    "Reduced bone mineral density",
                    "skeletal system phenotype",
                    "anatomical entity morphology phenotype",
                    "oxygen molecular entity",
                    "anatomical entity mass density phenotype",
                    "skeletal system morphology phenotype",
                    "bone element",
                    "skeletal element",
                    "aldohexose",
                    "Abnormality of the musculoskeletal system",
                    "lateral structure phenotype",
                    "Abnormality of bone mineral density",
                    "organ physiology phenotype",
                    "increased level of rac-lactic acid in urine",
                    "anatomical entity physiology phenotype",
                    "subdivision of organism along main body axis phenotype",
                    "metabolic process",
                    "nitrogen molecular entity",
                    "excretory tube",
                    "cavitated compound organ phenotype",
                    "renal system phenotype",
                    "musculoskeletal system",
                    "epithelial tube phenotype",
                    "kidney",
                    "anatomical system phenotype",
                    "biological_process",
                    "peptide",
                    "tube physiology phenotype",
                    "rac-lactic acid",
                    "Hypophosphatemia",
                    "blood cation level phenotype",
                    "presumptive structure phenotype",
                    "blood island",
                    "mesenchyme",
                    "organ phenotype",
                    "decreased level of potassium atom in blood",
                    "urine",
                    "Abnormal bone structure",
                    "organ part phenotype",
                    "anatomical system",
                    "skeletal system",
                    "Abnormal circulating metabolite concentration",
                    "Growth abnormality",
                    "phosphorus oxoacids and derivatives",
                    "multicellular organism phenotype",
                    "main group element atom",
                    "dense mesenchyme tissue phenotype",
                    "phosphorus molecular entity",
                    "haemolymphatic fluid phenotype",
                    "organ",
                    "germ layer phenotype",
                    "phosphoric acid derivative",
                    "blood chemical entity level phenotype",
                    "organochalcogen compound",
                    "Abnormality of the genitourinary system",
                    "blood phenotype",
                    "protein-containing molecular entity",
                    "cavitated compound organ",
                    "blood phosphate level phenotype",
                    "abdomen",
                    "hematopoietic system",
                    "Phenotypic abnormality",
                    "chemical entity",
                    "elemental molecular entity",
                    "upper urinary tract",
                    "genitourinary system",
                    "anatomical structure phenotype",
                    "Abnormality of urine homeostasis",
                    "presumptive structure",
                    "anatomical entity phenotype",
                    "racemate",
                    "skeletal element phenotype",
                    "anatomical structure physiology phenotype",
                    "anatomical system physiology phenotype",
                    "embryonic tissue phenotype",
                    "carbon group molecular entity",
                    "hemolymphoid system",
                    "main group molecular entity",
                    "polyatomic entity",
                    "inorganic cation",
                    "mesoderm-derived structure",
                    "lateral structure",
                    "germ layer",
                    "decreased functionality of the anatomical structure",
                    "continuant",
                    "abdominal segment element phenotype",
                    "dense mesenchyme tissue",
                    "developing anatomical structure phenotype",
                    "lateral plate mesoderm phenotype",
                    "epithelial tube",
                    "abdomen element",
                    "material anatomical entity",
                    "phosphate",
                    "Aminoaciduria",
                    "blood",
                    "epithelial tube physiology phenotype",
                    "blood island phenotype",
                    "mesoderm phenotype",
                    "All",
                    "material anatomical entity phenotype",
                    "material entity",
                    "Abnormality of the kidney",
                    "embryonic structure",
                    "compound organ physiology phenotype",
                    "Acidosis",
                    "anatomical entity height phenotype",
                    "organism subdivision",
                    "Abnormality of the musculature",
                    "role urine level phenotype",
                    "anatomical conduit",
                    "homeostatic process phenotype",
                    "tissue",
                    "abdominal segment of trunk",
                    "increased level of monosaccharide in urine",
                    "occurrent",
                    "Metabolic acidosis",
                    "Abnormality of acid-base homeostasis",
                    "tissue physiology phenotype",
                    "growth",
                    "entity",
                    "muscle organ",
                    "Abnormality of the urinary system",
                    "epithelium phenotype",
                    "organic molecular entity",
                    "ion",
                    "multicellular anatomical structure phenotype",
                    "protein polypeptide chain",
                    "Abnormality of metabolism/homeostasis",
                    "bodily fluid phenotype",
                    "tube",
                    "bodily fluid",
                    "genitourinary system phenotype",
                    "process",
                    "tissue phenotype",
                    "chemical substance",
                    "subdivision of organism along main body axis",
                    "bone element mass density phenotype",
                    "decreased functionality of the renal tubule",
                    "anatomical structure",
                    "decreased level of chemical entity in blood",
                    "heteroatomic molecular entity",
                    "renal system process",
                    "excretory tube physiology phenotype",
                    "multicellular anatomical structure",
                    "delayed biological_process",
                    "increased level of carboxylic acid in urine",
                    "multicellular organism chemical entity level phenotype",
                    "phenotype",
                    "Abnormal urinary electrolyte concentration",
                    "phosphate level phenotype",
                    "germ layer / neural crest",
                    "Abnormality of the skeletal system",
                    "hematopoietic system phenotype",
                    "decreased functionality of the nephron epithelium",
                    "anatomical conduit phenotype",
                    "organism substance phenotype",
                    "organonitrogen compound",
                    "lateral plate mesoderm",
                    "phosphorus oxoacid derivative",
                    "Abnormality of the upper urinary tract",
                    "renal absorption",
                    "increased level of chemical entity in urine",
                    "monoatomic entity",
                    "phenotypic effect",
                    "developing anatomical structure",
                    "decreased functionality of the tube",
                    "germ layer / neural crest phenotype",
                    "subdivision of trunk",
                    "multicellular organism",
                    "blood potassium atom level phenotype",
                    "biological_process phenotype",
                    "excretory system",
                    "oxoacid derivative",
                    "size of anatomical entity phenotype",
                    "anatomical entity",
                    "embryo",
                    "musculature of body",
                    "organ system subdivision phenotype",
                    "molecule",
                    "decreased level of chemical entity in tissue",
                    "mixture",
                    "taxon specific phenotype",
                    "molecular entity",
                    "carbohydrate",
                    "Abnormal homeostasis",
                    "blood monoatomic ion level phenotype",
                    "mesoderm",
                    "Abnormal blood ion concentration",
                    "musculoskeletal system phenotype",
                    "organ system subdivision",
                    "Abnormal urine metabolite level",
                    "tissue chemical entity level phenotype",
                    "nephron tubule",
                    "p-block molecular entity",
                    "amino acid",
                    "excretory tube phenotype",
                    "anatomical entity dysfunction in independent continuant",
                    "subdivision of trunk phenotype",
                    "Abnormal blood phosphate concentration",
                    "organ part",
                    "Abnormal blood cation concentration",
                    "anlage",
                    "nephron epithelium phenotype",
                    "growth phenotype",
                    "organism substance",
                    "decreased functionality of the epithelium",
                    "nitrogen molecular entity level phenotype",
                    "decreased functionality of the nephron tubule",
                    "decreased functionality of the multicellular anatomical structure",
                    "nephron tubule phenotype",
                    "Hypokalemia",
                    "upper urinary tract phenotype",
                    "main body axis",
                    "renal/urinary system phenotype",
                    "pnictogen molecular entity",
                    "epithelial vesicle",
                    "kidney epithelium",
                    "ossification",
                    "renal tubule phenotype",
                    "tube phenotype",
                    "blood monovalent inorganic cation level phenotype",
                    "anatomical conduit physiology phenotype",
                    "multicellular anatomical structure physiology phenotype",
                    "material anatomical entity physiology phenotype",
                    "body proper",
                    "cavitated compound organ physiology phenotype",
                    "decreased functionality of the anatomical conduit",
                    "trunk region element physiology phenotype",
                    "compound organ phenotype",
                    "increased level of chemical entity",
                    "decreased functionality of the material anatomical entity",
                    "abdominal segment element physiology phenotype",
                    "Abnormal urine amino acid level",
                    "decreased level of phosphate in blood",
                    "kidney phenotype",
                    "compound organ",
                    "Short stature",
                    "nephron",
                    "inorganic molecular entity",
                    "Osteomalacia",
                    "embryonic structure phenotype",
                    "epithelium physiology phenotype",
                    "lateral structure physiology phenotype",
                    "abdomen element physiology phenotype",
                    "increased level of alkaline phosphatase, tissue-nonspecific isozyme",
                    "kidney epithelium phenotype",
                    "mesoderm-derived structure phenotype",
                    "trunk region element phenotype",
                    "Muscle weakness",
                    "trunk",
                    "anlage phenotype",
                    "haemolymphatic fluid",
                    "alkali metal atom",
                    "nephron phenotype",
                    "trunk region element",
                    "epithelial vesicle phenotype",
                    "increased level of phosphate in urine",
                    "embryo phenotype",
                    "Abnormal renal physiology",
                    "kidney physiology phenotype",
                    "mesenchyme phenotype",
                    "Renal tubular dysfunction",
                    "nephron epithelium",
                    "renal system physiology phenotype",
                    "abdomen element phenotype",
                    "decreased functionality of the excretory tube",
                    "decreased functionality of the tissue",
                    "independent continuant",
                    "Abnormality of the urinary system physiology",
                    "monoatomic ion",
                    "trunk phenotype",
                    "epithelium",
                    "homeostatic process",
                    "kidney mesenchyme",
                    "organism subdivision phenotype",
                    "embryonic tissue",
                    "renal tubule",
                    "abdominal segment element",
                    "Hyperphosphaturia",
                    "decreased level of chemical entity",
                    "decreased functionality of the kidney epithelium",
                    "urine phosphate level phenotype",
                    "uriniferous tubule",
                    "Abnormal urine phosphate concentration",
                    "cellular process",
                    "urine chemical entity level phenotype",
                    "excreta",
                    "decreased size of the material anatomical entity",
                    "renal system",
                    "Abnormal urine pH",
                    "carbonyl compound",
                    "Aciduria",
                    "increased urine role level",
                    "organic molecule",
                    "kidney mesenchyme phenotype",
                    "potassium atom",
                    "Abnormal blood monovalent inorganic cation concentration",
                    "s-block element atom",
                    "atom",
                    "decreased functionality of the anatomical entity",
                    "decreased functionality of the epithelial tube",
                    "monovalent inorganic cation",
                    "Abnormal circulating potassium concentration",
                    "metal atom",
                    "Lacticaciduria",
                    "inorganic ion",
                    "amino acid level phenotype",
                    "cation",
                    "alkaline phosphatase, tissue-nonspecific isozyme",
                    "role blood level phenotype",
                    "decreased role blood level",
                    "chemical entity level phenotype",
                    "potassium atom level phenotype",
                    "role bodily fluid level phenotype",
                ],
                "has_phenotype_count": 16,
                "score": None,
                "exact_synonyms": [
                    "DeToni-Debré-Fanconi syndrome|FRTS1|Fanconi renotubular syndrome 1|primary Fanconi renal syndrome|primary Fanconi renotubular syndrome"
                ],
                "related_synonyms": [
                    "Fanconi renotubular syndrome|Fanconi syndrome without cystinosis|Luder-Sheldon syndrome|adult Fanconi syndrome|renal Fanconi syndrome"
                ],
                "highlighting": None,
            },
            {
                "id": "MONDO:0013247",
                "category": "biolink:Disease",
                "name": "Fanconi renotubular syndrome 2",
                "full_name": None,
                "deprecated": None,
                "description": "Any Fanconi syndrome in which the cause of the disease is a mutation in the SLC34A1 gene.",
                "xref": ["DOID:0080758", "GARD:15655", "MEDGEN:462002", "OMIM:613388", "UMLS:C3150652"],
                "provided_by": "phenio_nodes",
                "in_taxon": None,
                "in_taxon_label": None,
                "symbol": None,
                "synonym": [
                    "FRTS2",
                    "Fanconi renotubular syndrome 2",
                    "Fanconi renotubular syndrome type 2",
                    "Fanconi syndrome caused by mutation in SLC34A1",
                    "SLC34A1 Fanconi syndrome",
                ],
                "broad_synonym": None,
                "exact_synonym": None,
                "narrow_synonym": None,
                "related_synonym": None,
                "subsets": ["gard_rare", "nord_rare", "rare"],
                "uri": None,
                "iri": None,
                "namespace": "MONDO",
                "has_phenotype": [
                    "HP:0002148",
                    "HP:0000114",
                    "HP:0002757",
                    "HP:0002749",
                    "HP:0000117",
                    "HP:0002748",
                    "HP:0000938",
                    "HP:0002909",
                    "HP:0031415",
                    "HP:0000093",
                    "HP:0003076",
                    "HP:0003165",
                    "HP:0004322",
                    "HP:0002653",
                    "HP:0012213",
                    "HP:0002150",
                    "HP:0000083",
                ],
                "has_phenotype_label": [
                    "Hypophosphatemia",
                    "Proximal tubulopathy",
                    "Recurrent fractures",
                    "Osteomalacia",
                    "Renal phosphate wasting",
                    "Rickets",
                    "Osteopenia",
                    "Generalized aminoaciduria",
                    "High serum calcitriol",
                    "Proteinuria",
                    "Glycosuria",
                    "Elevated circulating parathyroid hormone level",
                    "Short stature",
                    "Bone pain",
                    "Decreased glomerular filtration rate",
                    "Hypercalciuria",
                    "Renal insufficiency",
                ],
                "has_phenotype_closure": [
                    "HP:0000083",
                    "HP:0002150",
                    "HP:0011280",
                    "UPHENO:0051712",
                    "HP:0012213",
                    "HP:0012212",
                    "UPHENO:0081423",
                    "UPHENO:0069254",
                    "HP:0001507",
                    "UPHENO:0080352",
                    "UPHENO:0081424",
                    "CHEBI:22313",
                    "UPHENO:0069062",
                    "HP:0001510",
                    "UPHENO:0075195",
                    "UPHENO:0080351",
                    "UPHENO:0068971",
                    "UPHENO:0049874",
                    "UPHENO:0069327",
                    "UBERON:0015204",
                    "UPHENO:0077826",
                    "PR:000013429",
                    "HP:0033331",
                    "UPHENO:0082541",
                    "UPHENO:0076285",
                    "HP:0004322",
                    "UPHENO:0068049",
                    "UPHENO:0082534",
                    "UPHENO:0051648",
                    "PR:000018263",
                    "PR:000000001",
                    "UBERON:0001969",
                    "UPHENO:0082536",
                    "CHEBI:15693",
                    "CHEBI:18133",
                    "UPHENO:0080658",
                    "UPHENO:0051635",
                    "HP:6000531",
                    "HP:0003117",
                    "UPHENO:0068054",
                    "UBERON:0034923",
                    "HP:0003076",
                    "CHEBI:33839",
                    "UPHENO:0000541",
                    "UPHENO:0052038",
                    "CHEBI:15841",
                    "HP:0000818",
                    "HP:0000093",
                    "CHEBI:32988",
                    "CHEBI:33256",
                    "HP:0003165",
                    "CHEBI:37622",
                    "HP:0020129",
                    "CHEBI:73558",
                    "UPHENO:0068047",
                    "UPHENO:0089759",
                    "UPHENO:0050121",
                    "GO:0008202",
                    "HP:0012531",
                    "CHEBI:33595",
                    "HP:0031415",
                    "CHEBI:17234",
                    "UPHENO:0089764",
                    "UPHENO:0077817",
                    "CHEBI:35341",
                    "CHEBI:26191",
                    "CHEBI:35350",
                    "CHEBI:51958",
                    "GO:0044281",
                    "HP:0100508",
                    "CHEBI:33917",
                    "UPHENO:0068251",
                    "CHEBI:33822",
                    "CHEBI:33318",
                    "HP:0100511",
                    "CHEBI:27300",
                    "CHEBI:36853",
                    "CHEBI:16541",
                    "GO:0006766",
                    "UPHENO:0068556",
                    "UPHENO:0068064",
                    "CHEBI:16670",
                    "GO:0006629",
                    "UPHENO:0049618",
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                    "UPHENO:0079534",
                    "UPHENO:0046291",
                    "HP:0032245",
                    "UPHENO:0068491",
                    "CHEBI:33608",
                    "CHEBI:33304",
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                    "CHEBI:72695",
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                    "CHEBI:78616",
                    "HP:0003355",
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                    "UBERON:0015203",
                    "HP:0025745",
                    "UPHENO:3000004",
                    "UBERON:0001008",
                    "UBERON:0000062",
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                    "CHEBI:33521",
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                    "CHEBI:35788",
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                    "UPHENO:0046281",
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                    "CHEBI:33559",
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                    "CHEBI:23367",
                    "CHEBI:17823",
                    "UPHENO:0051804",
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                    "CHEBI:24867",
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                    "CHEBI:26082",
                    "UBERON:0001977",
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                    "UBERON:0001231",
                    "UPHENO:0052002",
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                    "BFO:0000003",
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                    "CHEBI:36357",
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                    "CHEBI:33709",
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                    "UBERON:0002204",
                    "CHEBI:47042",
                    "CHEBI:24870",
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                    "HP:0012599",
                    "UBERON:0001015",
                    "HP:0011843",
                    "CHEBI:16646",
                    "HP:0002659",
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                    "CHEBI:24431",
                    "UPHENO:0081440",
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                    "UPHENO:0080643",
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                    "HP:0011842",
                    "UPHENO:0001001",
                    "UPHENO:0002442",
                    "HP:0003330",
                    "UPHENO:0084653",
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                    "UPHENO:0082539",
                    "UPHENO:0002346",
                    "HP:0011849",
                    "GO:0006775",
                    "UPHENO:0002754",
                    "UPHENO:0002870",
                    "UPHENO:0002559",
                    "UPHENO:0002311",
                    "HP:0004349",
                    "HP:0002749",
                    "UPHENO:0076692",
                    "CHEBI:22984",
                    "CHEBI:27136",
                    "UPHENO:0051900",
                    "UPHENO:0002571",
                    "UBERON:0005291",
                    "HP:0000117",
                    "CHEBI:18059",
                    "HP:0012591",
                ],
                "has_phenotype_closure_label": [
                    "Renal insufficiency",
                    "Hypercalciuria",
                    "s-block element atom",
                    "main group element atom",
                    "atom",
                    "Decreased glomerular filtration rate",
                    "Bone pain",
                    "Constitutional symptom",
                    "Abnormality of body height",
                    "decreased size of the multicellular anatomical structure",
                    "delayed growth",
                    "decreased size of the anatomical entity",
                    "Abnormality of urine calcium concentration",
                    "decreased height of the multicellular organism",
                    "multicellular organism height phenotype",
                    "decreased height of the anatomical entity",
                    "metal atom",
                    "Elevated circulating parathyroid hormone level",
                    "Abnormal circulating hormone concentration",
                    "endocrine system phenotype",
                    "disconnected anatomical group",
                    "blood nitrogen molecular entity level phenotype",
                    "increased level of nitrogen molecular entity in blood",
                    "increased bodily fluid base level",
                    "blood plasma",
                    "blood serum",
                    "protein",
                    "increased blood serum role level",
                    "blood organic amino compound level phenotype",
                    "endocrine system",
                    "non-connected functional system",
                    "blood parathyroid hormone level phenotype",
                    "Acute phase response",
                    "parathyroid hormone",
                    "blood serum chemical entity level phenotype",
                    "glucose",
                    "aldose",
                    "hexose",
                    "monosaccharide",
                    "Glycosuria",
                    "Abnormal urinary organic compound level",
                    "increased level of glucose in urine",
                    "urine glucose level phenotype",
                    "Abnormal urine protein level",
                    "Growth delay",
                    "amide",
                    "urine calcium atom level phenotype",
                    "macromolecule",
                    "primary amide",
                    "carboxamide",
                    "Proteinuria",
                    "increased level of parathyroid hormone in blood",
                    "polypeptide",
                    "increased level of protein polypeptide chain in urine",
                    "steroid",
                    "polyol",
                    "vitamin D level phenotype",
                    "vitamin metabolic process phenotype",
                    "increased level of chemical entity in blood",
                    "Abnormality of vitamin D metabolism",
                    "role blood level phenotype",
                    "vitamin D metabolic process phenotype",
                    "decreased size of the anatomical structure",
                    "carbohydrates and carbohydrate derivatives",
                    "increased level of lipid",
                    "increased blood role level",
                    "increased level of chemical entity in bodily fluid",
                    "increased level of chemical entity in blood serum",
                    "lipid metabolic process",
                    "vitamin metabolic process",
                    "vitamin D",
                    "blood plasma chemical entity level phenotype",
                    "hydroxycalciol",
                    "calcitriol",
                    "hydroxy seco-steroid",
                    "triol",
                    "primary metabolic process",
                    "blood organic molecular entity level phenotype",
                    "increased bodily fluid role level",
                    "blood lipid level phenotype",
                    "increased level of vitamin D",
                    "High serum calcitriol",
                    "polycyclic compound",
                    "organic cyclic compound",
                    "hormone blood level phenotype",
                    "role bodily fluid level phenotype",
                    "increased level of chemical entity in tissue",
                    "increased level of calcitriol in blood",
                    "decreased size of the multicellular organism",
                    "small molecule metabolic process phenotype",
                    "increased urine role level",
                    "amino acid level phenotype",
                    "organooxygen compound",
                    "heteroorganic entity",
                    "carbon oxoacid",
                    "carbonyl compound",
                    "increased level of chemical entity",
                    "increased level of organic acid in urine",
                    "s-block molecular entity",
                    "increased level of chemical entity in urine",
                    "Generalized aminoaciduria",
                    "carboxylic acid",
                    "organic acid",
                    "oxoacid",
                    "organic oxo compound",
                    "increased level of amino acid in urine",
                    "hydrogen molecular entity",
                    "urine amino acid level phenotype",
                    "chalcogen molecular entity",
                    "anatomical entity dysfunction in independent continuant",
                    "subdivision of trunk phenotype",
                    "lateral structure phenotype",
                    "increased level of parathyroid hormone in blood serum",
                    "anatomical entity physiology phenotype",
                    "subdivision of organism along main body axis phenotype",
                    "excretory system",
                    "biological_process phenotype",
                    "metabolic process",
                    "nitrogen molecular entity",
                    "excretory tube",
                    "cavitated compound organ phenotype",
                    "renal system phenotype",
                    "kidney",
                    "anatomical system phenotype",
                    "lipid level phenotype",
                    "anatomical entity morphology phenotype",
                    "biological_process",
                    "chemical entity level phenotype",
                    "peptide",
                    "tube physiology phenotype",
                    "tube",
                    "bodily fluid",
                    "Hypophosphatemia",
                    "size of multicellular organism phenotype",
                    "amino acid chain",
                    "Renal phosphate wasting",
                    "presumptive structure phenotype",
                    "D3 vitamins",
                    "blood island",
                    "genitourinary system phenotype",
                    "process",
                    "mesenchyme",
                    "organ phenotype",
                    "urine",
                    "Growth abnormality",
                    "phosphorus oxoacids and derivatives",
                    "multicellular organism phenotype",
                    "Aminoaciduria",
                    "blood",
                    "epithelial tube physiology phenotype",
                    "vitamin D metabolic process",
                    "germ layer",
                    "multicellular organism morphology phenotype",
                    "dense mesenchyme tissue phenotype",
                    "phosphorus molecular entity",
                    "homeostatic process phenotype",
                    "haemolymphatic fluid phenotype",
                    "organ",
                    "germ layer phenotype",
                    "phosphoric acid derivative",
                    "blood chemical entity level phenotype",
                    "organochalcogen compound",
                    "Abnormality of the genitourinary system",
                    "Abnormal metabolism",
                    "blood phenotype",
                    "protein-containing molecular entity",
                    "cavitated compound organ",
                    "blood phosphate level phenotype",
                    "phenotype",
                    "Abnormal urinary electrolyte concentration",
                    "abdomen",
                    "hematopoietic system",
                    "Phenotypic abnormality",
                    "chemical entity",
                    "lipid",
                    "elemental molecular entity",
                    "increased level of monosaccharide in urine",
                    "occurrent",
                    "upper urinary tract",
                    "genitourinary system",
                    "Rickets",
                    "Abnormality of urine homeostasis",
                    "presumptive structure",
                    "anatomical entity phenotype",
                    "tissue physiology phenotype",
                    "growth",
                    "entity",
                    "Abnormality of the urinary system",
                    "epithelium phenotype",
                    "Abnormality of the kidney",
                    "carbohydrate",
                    "blood monoatomic ion level phenotype",
                    "molecular entity",
                    "anatomical system physiology phenotype",
                    "Proximal tubulopathy",
                    "cellular process phenotype",
                    "oxoacid derivative",
                    "mesoderm-derived structure",
                    "continuant",
                    "decreased functionality of the anatomical structure",
                    "lateral structure",
                    "embryonic tissue phenotype",
                    "carbon group molecular entity",
                    "hemolymphoid system",
                    "heteroatomic molecular entity",
                    "anatomical conduit phenotype",
                    "organism substance phenotype",
                    "organonitrogen compound",
                    "lateral plate mesoderm",
                    "phosphorus oxoacid derivative",
                    "Abnormality of the upper urinary tract",
                    "monoatomic entity",
                    "glandular system",
                    "multicellular anatomical structure",
                    "excretory tube physiology phenotype",
                    "material anatomical entity phenotype",
                    "organ physiology phenotype",
                    "Abnormality of bone mineral density",
                    "tissue phenotype",
                    "subdivision of organism along main body axis",
                    "material anatomical entity",
                    "phosphate",
                    "abdominal segment element phenotype",
                    "musculoskeletal system physiology phenotype",
                    "material entity",
                    "multicellular organismal process",
                    "increased blood serum base level",
                    "phenotypic effect",
                    "developing anatomical structure",
                    "decreased functionality of the tube",
                    "germ layer / neural crest phenotype",
                    "subdivision of trunk",
                    "small molecule metabolic process",
                    "embryo",
                    "trunk",
                    "anlage phenotype",
                    "haemolymphatic fluid",
                    "Osteopenia",
                    "molecule",
                    "decreased level of chemical entity in tissue",
                    "bodily fluid phenotype",
                    "organic molecular entity",
                    "ion",
                    "multicellular anatomical structure phenotype",
                    "protein polypeptide chain",
                    "Abnormality of metabolism/homeostasis",
                    "tissue",
                    "abdominal segment of trunk",
                    "size of anatomical entity phenotype",
                    "anatomical entity",
                    "embryonic structure",
                    "compound organ physiology phenotype",
                    "germ layer / neural crest",
                    "lateral plate mesoderm phenotype",
                    "epithelial tube",
                    "abdomen element",
                    "calcium atom level phenotype",
                    "taxon specific phenotype",
                    "multicellular organism",
                    "decreased functionality of the renal tubule",
                    "anatomical structure",
                    "bone element mass density phenotype",
                    "mesoderm",
                    "Recurrent fractures",
                    "Abnormal blood ion concentration",
                    "Abnormal urine metabolite level",
                    "tissue chemical entity level phenotype",
                    "polyatomic entity",
                    "phosphate level phenotype",
                    "nephron tubule",
                    "alkaline earth metal atom",
                    "p-block molecular entity",
                    "amino acid",
                    "excretory tube phenotype",
                    "organ part phenotype",
                    "anatomical system",
                    "Abnormal bone structure",
                    "organic polycyclic compound",
                    "decreased level of chemical entity in blood",
                    "Pain",
                    "main group molecular entity",
                    "dense mesenchyme tissue",
                    "calcium atom",
                    "developing anatomical structure phenotype",
                    "musculature",
                    "mesoderm phenotype",
                    "All",
                    "blood island phenotype",
                    "Abnormal blood phosphate concentration",
                    "organ part",
                    "anlage",
                    "Abnormality of vitamin metabolism",
                    "nephron epithelium phenotype",
                    "growth phenotype",
                    "organism substance",
                    "decreased functionality of the epithelium",
                    "nitrogen molecular entity level phenotype",
                    "decreased functionality of the nephron tubule",
                    "decreased functionality of the multicellular anatomical structure",
                    "nephron tubule phenotype",
                    "upper urinary tract phenotype",
                    "main body axis",
                    "Abnormal circulating calcium-phosphate regulating hormone concentration",
                    "renal/urinary system phenotype",
                    "pnictogen molecular entity",
                    "epithelial vesicle",
                    "kidney epithelium",
                    "ossification",
                    "renal tubule phenotype",
                    "tube phenotype",
                    "anatomical entity height phenotype",
                    "Abnormality of the endocrine system",
                    "cyclic compound",
                    "organism subdivision",
                    "hydroxy steroid",
                    "metabolic process phenotype",
                    "role urine level phenotype",
                    "anatomical conduit",
                    "anatomical conduit physiology phenotype",
                    "multicellular anatomical structure physiology phenotype",
                    "Abnormal glomerular filtration rate",
                    "material anatomical entity physiology phenotype",
                    "body proper",
                    "organic hydroxy compound",
                    "cavitated compound organ physiology phenotype",
                    "decreased functionality of the anatomical conduit",
                    "trunk region element physiology phenotype",
                    "compound organ phenotype",
                    "decreased size of the material anatomical entity",
                    "renal system",
                    "decreased functionality of the material anatomical entity",
                    "abdominal segment element physiology phenotype",
                    "Abnormal urine amino acid level",
                    "decreased level of phosphate in blood",
                    "kidney phenotype",
                    "compound organ",
                    "Short stature",
                    "nephron",
                    "lateral structure physiology phenotype",
                    "abdomen element physiology phenotype",
                    "bone element phenotype",
                    "kidney epithelium phenotype",
                    "hematopoietic system phenotype",
                    "decreased functionality of the nephron epithelium",
                    "Abnormality of the skeletal system",
                    "mesoderm-derived structure phenotype",
                    "trunk region element phenotype",
                    "nephron phenotype",
                    "trunk region element",
                    "epithelial vesicle phenotype",
                    "decreased functionality of the anatomical entity",
                    "decreased functionality of the epithelial tube",
                    "embryo phenotype",
                    "Abnormal renal physiology",
                    "Abnormal bone ossification",
                    "kidney physiology phenotype",
                    "hydroxides",
                    "mesenchyme phenotype",
                    "Renal tubular dysfunction",
                    "nephron epithelium",
                    "renal system physiology phenotype",
                    "abdomen element phenotype",
                    "decreased functionality of the excretory tube",
                    "decreased functionality of the tissue",
                    "independent continuant",
                    "Abnormality of the urinary system physiology",
                    "monoatomic ion",
                    "trunk phenotype",
                    "epithelium",
                    "steroid metabolic process",
                    "kidney mesenchyme",
                    "homeostatic process",
                    "organism subdivision phenotype",
                    "embryonic tissue",
                    "renal tubule",
                    "fat-soluble vitamin metabolic process",
                    "abdominal segment element",
                    "aldohexose",
                    "Abnormality of the musculoskeletal system",
                    "epithelial tube phenotype",
                    "musculoskeletal system",
                    "skeletal element",
                    "excreta",
                    "bone element",
                    "seco-steroid",
                    "Abnormal musculoskeletal physiology",
                    "organ system subdivision",
                    "musculoskeletal system phenotype",
                    "increased level of lipid in blood",
                    "musculature phenotype",
                    "role blood serum level phenotype",
                    "musculature of body phenotype",
                    "anatomical structure phenotype",
                    "Increased susceptibility to fractures",
                    "Abnormal circulating metabolite concentration",
                    "skeletal system",
                    "organ system subdivision phenotype",
                    "musculature of body",
                    "blood oxygen molecular entity level phenotype",
                    "skeletal system morphology phenotype",
                    "embryonic structure phenotype",
                    "epithelium physiology phenotype",
                    "Osteomalacia",
                    "increased level of calcium atom in urine",
                    "oxygen molecular entity",
                    "anatomical entity mass density phenotype",
                    "skeletal system phenotype",
                    "delayed biological_process",
                    "multicellular organism chemical entity level phenotype",
                    "increased level of carboxylic acid in urine",
                    "increased level of chemical entity in blood plasma",
                    "organic amino compound",
                    "Reduced bone mineral density",
                    "anatomical structure physiology phenotype",
                    "skeletal element phenotype",
                    "Decreased anatomical entity mass density",
                    "Abnormal skeletal morphology",
                    "Decreased bone element mass density",
                    "decreased level of chemical entity",
                    "decreased functionality of the kidney epithelium",
                    "urine phosphate level phenotype",
                    "uriniferous tubule",
                    "Abnormal urine phosphate concentration",
                    "cellular process",
                    "urine chemical entity level phenotype",
                    "kidney mesenchyme phenotype",
                    "organic molecule",
                ],
                "has_phenotype_count": 17,
                "score": None,
                "exact_synonyms": [
                    "Fanconi renotubular syndrome 2|Fanconi renotubular syndrome type 2|Fanconi syndrome caused by mutation in SLC34A1|SLC34A1 Fanconi syndrome"
                ],
                "related_synonyms": ["FRTS2"],
                "highlighting": None,
            },
            {
                "id": "MONDO:0100238",
                "category": "biolink:Disease",
                "name": "inherited Fanconi renotubular syndrome",
                "full_name": None,
                "deprecated": None,
                "description": "An instance of Fanconi renotubular syndrome that is inherited.",
                "xref": ["OMIMPS:134600"],
                "provided_by": "phenio_nodes",
                "in_taxon": None,
                "in_taxon_label": None,
                "symbol": None,
                "synonym": ["hereditary Fanconi renotubular syndrome"],
                "broad_synonym": None,
                "exact_synonym": None,
                "narrow_synonym": None,
                "related_synonym": None,
                "subsets": ["gard_rare", "rare"],
                "uri": None,
                "iri": None,
                "namespace": "MONDO",
                "has_phenotype": None,
                "has_phenotype_label": None,
                "has_phenotype_closure": None,
                "has_phenotype_closure_label": None,
                "has_phenotype_count": 0,
                "score": None,
                "exact_synonyms": ["hereditary Fanconi renotubular syndrome"],
                "highlighting": None,
            },
            {
                "id": "HP:0001994",
                "category": "biolink:PhenotypicFeature",
                "name": "Renal Fanconi syndrome",
                "full_name": None,
                "deprecated": None,
                "description": "An inability of the tubules in the kidney to reabsorb small molecules, causing increased urinary loss of electrolytes (sodium, potassium, bicarbonate), minerals, glucose, amino acids, and water.",
                "xref": ["SNOMEDCT_US:236468006", "SNOMEDCT_US:44673006", "UMLS:C0341703"],
                "provided_by": "phenio_nodes",
                "in_taxon": None,
                "in_taxon_label": None,
                "symbol": None,
                "synonym": ["De toni-fanconi-debre syndrome", "Renal tubular fanconi syndrome"],
                "broad_synonym": None,
                "exact_synonym": None,
                "narrow_synonym": None,
                "related_synonym": None,
                "subsets": None,
                "uri": None,
                "iri": None,
                "namespace": "HP",
                "has_phenotype": None,
                "has_phenotype_label": None,
                "has_phenotype_closure": None,
                "has_phenotype_closure_label": None,
                "has_phenotype_count": 0,
                "score": None,
                "exact_synonyms": ["De toni-fanconi-debre syndrome|Renal tubular fanconi syndrome"],
                "highlighting": None,
            },
            {
                "id": "MONDO:0010953",
                "category": "biolink:Disease",
                "name": "Fanconi anemia complementation group E",
                "full_name": None,
                "deprecated": None,
                "description": "Fanconi anemia caused by mutations of the FANCE gene. This is a protein coding gene. It is required for the nuclear accumulation of FANCC and provides a critical bridge between the FA complex and FANCD2.",
                "xref": ["DOID:0111084", "GARD:15324", "MEDGEN:463628", "NCIT:C125709", "OMIM:600901", "UMLS:C3160739"],
                "provided_by": "phenio_nodes",
                "in_taxon": None,
                "in_taxon_label": None,
                "symbol": None,
                "synonym": [
                    "FACE",
                    "FANCE",
                    "FANCE Fanconi anaemia",
                    "FANCE Fanconi anemia",
                    "Fanconi Anemia, complementation group type E",
                    "Fanconi anaemia caused by mutation in FANCE",
                    "Fanconi anaemia complementation group type E",
                    "Fanconi anemia caused by mutation in FANCE",
                    "Fanconi anemia complementation group E",
                    "Fanconi anemia complementation group type E",
                    "Fanconi anemia, complementation group E",
                    "face",
                ],
                "broad_synonym": None,
                "exact_synonym": None,
                "narrow_synonym": None,
                "related_synonym": None,
                "subsets": ["clingen", "gard_rare", "nord_rare", "otar", "rare"],
                "uri": None,
                "iri": None,
                "namespace": "MONDO",
                "has_phenotype": [
                    "HP:0000104",
                    "HP:0001875",
                    "HP:0001017",
                    "HP:0001876",
                    "HP:0000028",
                    "HP:0003974",
                    "HP:0001873",
                    "HP:0009778",
                    "HP:0001896",
                    "HP:0009777",
                    "HP:0000568",
                    "HP:0001518",
                    "HP:0001263",
                    "HP:0003221",
                    "HP:0000252",
                    "HP:0001249",
                    "HP:0009943",
                    "HP:0000978",
                    "HP:0001627",
                    "HP:0000953",
                    "HP:0000957",
                    "HP:0001903",
                    "HP:0000815",
                    "HP:0001909",
                    "HP:0000081",
                    "HP:0000086",
                    "HP:0004322",
                    "HP:0000486",
                    "HP:0000365",
                    "HP:0003214",
                    "HP:0003213",
                    "HP:0000085",
                ],
                "has_phenotype_label": [
                    "Renal agenesis",
                    "Decreased total neutrophil count",
                    "Anemic pallor",
                    "Pancytopenia",
                    "Cryptorchidism",
                    "Absent radius",
                    "Thrombocytopenia",
                    "Short thumb",
                    "Reticulocytopenia",
                    "Absent thumb",
                    "Microphthalmia",
                    "Small for gestational age",
                    "Global developmental delay",
                    "Chromosomal breakage induced by crosslinking agents",
                    "Microcephaly",
                    "Intellectual disability",
                    "Complete duplication of thumb phalanx",
                    "Bruising susceptibility",
                    "Abnormal heart morphology",
                    "Hyperpigmentation of the skin",
                    "Cafe-au-lait spot",
                    "Anemia",
                    "Hypergonadotropic hypogonadism",
                    "Leukemia",
                    "Duplicated collecting system",
                    "Ectopic kidney",
                    "Short stature",
                    "Strabismus",
                    "Hearing impairment",
                    "Prolonged G2 phase of cell cycle",
                    "Deficient excision of UV-induced pyrimidine dimers in DNA",
                    "Horseshoe kidney",
                ],
                "has_phenotype_closure": [
                    "UPHENO:0080300",
                    "UPHENO:0076941",
                    "HP:0000085",
                    "UPHENO:0041465",
                    "UPHENO:0041226",
                    "UPHENO:0041629",
                    "GO:0050896",
                    "GO:0006259",
                    "UPHENO:0051124",
                    "UPHENO:0049720",
                    "UPHENO:0049586",
                    "GO:0033554",
                    "GO:0051716",
                    "GO:0006950",
                    "GO:0006139",
                    "GO:0006974",
                    "UPHENO:0049671",
                    "GO:0051319",
                    "GO:0051325",
                    "GO:0050954",
                    "UPHENO:0005433",
                    "UPHENO:0050234",
                    "UPHENO:0005437",
                    "UPHENO:0002240",
                    "UPHENO:0052161",
                    "HP:0012373",
                    "UBERON:0010222",
                    "UBERON:0000466",
                    "UPHENO:0002430",
                    "UPHENO:0005512",
                    "GO:0007610",
                    "UPHENO:0002301",
                    "UPHENO:0002360",
                    "UPHENO:0049622",
                    "NBO:0000444",
                    "BFO:0000141",
                    "UBERON:0006800",
                    "UBERON:0000015",
                    "UPHENO:0002403",
                    "UPHENO:0069254",
                    "UPHENO:0000543",
                    "HP:0000002",
                    "UPHENO:0053619",
                    "UPHENO:0053633",
                    "UPHENO:0053643",
                    "GO:0044848",
                    "HP:0000086",
                    "UPHENO:0075787",
                    "UBERON:0004100",
                    "UBERON:0003918",
                    "UBERON:0007688",
                    "HP:0002664",
                    "HP:0004377",
                    "UPHENO:0002378",
                    "UPHENO:0002206",
                    "HP:0000080",
                    "UPHENO:0002386",
                    "HP:0011793",
                    "UBERON:0000949",
                    "UPHENO:0024906",
                    "UPHENO:0066902",
                    "UPHENO:0066903",
                    "UPHENO:0002381",
                    "UPHENO:0066972",
                    "HP:0008373",
                    "HP:0000957",
                    "HP:0007400",
                    "HP:0012733",
                    "HP:0001034",
                    "GO:0043473",
                    "UPHENO:0074584",
                    "UPHENO:0054970",
                    "UPHENO:0080662",
                    "UPHENO:0074575",
                    "UPHENO:0003086",
                    "UPHENO:0081423",
                    "UBERON:0000948",
                    "UBERON:0005178",
                    "UPHENO:0002634",
                    "HP:0001903",
                    "HP:0030680",
                    "UBERON:0015228",
                    "HP:0000978",
                    "UPHENO:0002576",
                    "UPHENO:0076810",
                    "MPATH:603",
                    "HP:0011276",
                    "UBERON:0004535",
                    "UBERON:0011818",
                    "UBERON:0001009",
                    "UBERON:0007798",
                    "UBERON:0000477",
                    "UPHENO:9002003",
                    "HP:0009998",
                    "UBERON:0010688",
                    "UBERON:5106048",
                    "MPATH:1000",
                    "UBERON:0012151",
                    "UBERON:0015063",
                    "UBERON:0015204",
                    "UBERON:0003620",
                    "HP:0001000",
                    "UBERON:0001436",
                    "UBERON:0012357",
                    "UBERON:0005897",
                    "MPATH:120",
                    "HP:0005918",
                    "HP:0009942",
                    "UBERON:5101463",
                    "UBERON:0015023",
                    "UBERON:0015024",
                    "GO:0007049",
                    "UBERON:0011250",
                    "HP:0009602",
                    "HP:0001510",
                    "UPHENO:0066905",
                    "UBERON:0010543",
                    "UBERON:5102544",
                    "HP:0009142",
                    "GO:0003008",
                    "GO:0050890",
                    "HP:0011446",
                    "UPHENO:0080377",
                    "UBERON:0001893",
                    "HP:0000240",
                    "UPHENO:0087518",
                    "UPHENO:0076791",
                    "UPHENO:0049964",
                    "UPHENO:0002859",
                    "UPHENO:0076805",
                    "HP:0002060",
                    "HP:0000818",
                    "HP:0000929",
                    "HP:0002977",
                    "UPHENO:0002668",
                    "UPHENO:0075804",
                    "UPHENO:0005285",
                    "UBERON:0003914",
                    "HP:0012639",
                    "HP:0040195",
                    "UBERON:0005944",
                    "UBERON:0002090",
                    "UBERON:0001690",
                    "UBERON:0011138",
                    "UBERON:0000025",
                    "UPHENO:0004507",
                    "UPHENO:0004484",
                    "UBERON:0001049",
                    "UBERON:0003080",
                    "UPHENO:0081566",
                    "HP:0000152",
                    "UBERON:0002616",
                    "UPHENO:0076702",
                    "UPHENO:3000000",
                    "HP:0011018",
                    "UPHENO:0003004",
                    "UPHENO:0002736",
                    "UPHENO:0076799",
                    "UPHENO:0050065",
                    "HP:0003220",
                    "HP:0025354",
                    "GO:0060255",
                    "GO:0010467",
                    "GO:0048519",
                    "GO:0043170",
                    "GO:0008152",
                    "UPHENO:0052159",
                    "HP:0001939",
                    "UPHENO:0050007",
                    "GO:0031049",
                    "UPHENO:0052160",
                    "GO:0009059",
                    "GO:0005623",
                    "UPHENO:0078606",
                    "HP:0040012",
                    "UPHENO:0049837",
                    "UPHENO:0076776",
                    "UPHENO:0049835",
                    "HP:0003221",
                    "UPHENO:0049652",
                    "UPHENO:0002385",
                    "UPHENO:0003001",
                    "UPHENO:0004523",
                    "UBERON:0001016",
                    "HP:0001263",
                    "UPHENO:0002267",
                    "UPHENO:0002269",
                    "UBERON:0002105",
                    "UPHENO:0002433",
                    "UPHENO:0053588",
                    "UPHENO:0082761",
                    "UPHENO:0010850",
                    "UPHENO:0075220",
                    "BFO:0000015",
                    "UPHENO:0002211",
                    "UPHENO:0054374",
                    "GO:0008150",
                    "GO:0040007",
                    "HP:0001518",
                    "HP:0004322",
                    "BFO:0000003",
                    "UPHENO:0049874",
                    "UPHENO:0010763",
                    "UPHENO:0010799",
                    "UBERON:0000490",
                    "NCBITaxon:33208",
                    "UBERON:0001048",
                    "UBERON:0001444",
                    "UBERON:0002346",
                    "UBERON:0001032",
                    "UPHENO:0050008",
                    "UPHENO:0005097",
                    "UBERON:0000481",
                    "UBERON:0002049",
                    "NCBITaxon:131567",
                    "UPHENO:0002866",
                    "UPHENO:0004757",
                    "UPHENO:0086679",
                    "HP:0008056",
                    "UPHENO:0003186",
                    "UBERON:0001456",
                    "UBERON:0007811",
                    "UBERON:0004088",
                    "UBERON:0010312",
                    "UPHENO:0002844",
                    "UPHENO:0005110",
                    "HP:0100887",
                    "UPHENO:0002910",
                    "UPHENO:0003236",
                    "UBERON:0002104",
                    "UPHENO:0005058",
                    "UPHENO:0004494",
                    "UBERON:0003129",
                    "UBERON:0000924",
                    "UPHENO:0004721",
                    "UPHENO:0087472",
                    "UPHENO:0086486",
                    "UBERON:0001890",
                    "UBERON:0003072",
                    "UBERON:0000047",
                    "UBERON:0016879",
                    "NCBITaxon:2759",
                    "UPHENO:0004519",
                    "UPHENO:0002928",
                    "UBERON:0000483",
                    "HP:0000496",
                    "UPHENO:0066945",
                    "UPHENO:0068914",
                    "UPHENO:0075997",
                    "UPHENO:0000541",
                    "UBERON:0000020",
                    "UPHENO:0003189",
                    "UPHENO:0069064",
                    "UBERON:0000970",
                    "UPHENO:0005055",
                    "UBERON:0002075",
                    "HP:0000568",
                    "UPHENO:0004888",
                    "UPHENO:0009146",
                    "HP:0009777",
                    "UPHENO:0011825",
                    "UPHENO:0002678",
                    "UPHENO:0009382",
                    "UPHENO:0026108",
                    "CL:0000558",
                    "UPHENO:0088162",
                    "CL:0002422",
                    "HP:0004312",
                    "GO:0010629",
                    "HP:0001877",
                    "UBERON:5002544",
                    "UPHENO:0002733",
                    "UPHENO:0012308",
                    "UPHENO:0053601",
                    "HP:0006265",
                    "UBERON:0000033",
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                    "UPHENO:0080325",
                    "UPHENO:0012312",
                    "UPHENO:0008548",
                    "UPHENO:0046528",
                    "HP:0001896",
                    "UPHENO:0046426",
                    "HP:0032251",
                    "UBERON:0010740",
                    "UPHENO:0068971",
                    "UPHENO:0002595",
                    "UPHENO:0046707",
                    "UPHENO:0002803",
                    "UPHENO:0002782",
                    "UBERON:5002389",
                    "UBERON:0002544",
                    "UPHENO:0084761",
                    "UBERON:0002513",
                    "HP:0011297",
                    "GO:0010468",
                    "UPHENO:0046505",
                    "HP:0001167",
                    "UBERON:5001463",
                    "UBERON:0006717",
                    "UPHENO:0069236",
                    "UPHENO:0008545",
                    "UBERON:0005451",
                ],
                "has_phenotype_closure_label": [
                    "Horseshoe kidney",
                    "shape of anatomical entity phenotype",
                    "concave 3-D shape anatomical entity",
                    "response to stimulus phenotype",
                    "cellular response to stimulus phenotype",
                    "response to stimulus",
                    "nucleobase-containing compound metabolic process",
                    "DNA damage response",
                    "primary metabolic process",
                    "cellular response to stress",
                    "DNA repair phenotype",
                    "DNA metabolic process phenotype",
                    "response to stress",
                    "Deficient excision of UV-induced pyrimidine dimers in DNA",
                    "Abnormality of the cell cycle",
                    "cell cycle phase",
                    "cell cycle",
                    "decreased sensory perception of mechanical stimulus",
                    "decreased nervous system process",
                    "decreased biological_process",
                    "Hearing impairment",
                    "nervous system process phenotype",
                    "decreased multicellular organismal process",
                    "ear physiology phenotype",
                    "sensory perception of sound",
                    "decreased sensory perception of sound",
                    "decreased qualitatively sensory perception of sound",
                    "sensory perception of mechanical stimulus",
                    "immaterial entity",
                    "structure with developmental contribution from neural crest physiology phenotype",
                    "Abnormality of DNA repair",
                    "anatomical line between pupils",
                    "lateral structure physiology phenotype",
                    "simple eye physiology phenotype",
                    "Abnormal eye physiology",
                    "Abnormality of eye movement",
                    "ectoderm-derived structure physiology phenotype",
                    "decreased size of the multicellular organism",
                    "DNA repair",
                    "anatomical entity height phenotype",
                    "delayed biological_process",
                    "Short stature",
                    "decreased height of the multicellular organism",
                    "Growth delay",
                    "localised trunk region element",
                    "localised cavitated compound organ",
                    "Ectopic kidney",
                    "kidney mesenchyme",
                    "anlage phenotype",
                    "Abnormal renal collecting system morphology",
                    "kidney mesenchyme phenotype",
                    "endocrine system phenotype",
                    "Abnormality of reproductive system physiology",
                    "decreased functionality of the organ",
                    "multicellular anatomical structure physiology phenotype",
                    "decreased functionality of the reproductive structure",
                    "Hypergonadotropic hypogonadism",
                    "organ physiology phenotype",
                    "decreased functionality of the anatomical entity",
                    "reproductive structure physiology phenotype",
                    "decreased functionality of the reproductive organ",
                    "reproductive organ physiology phenotype",
                    "gonad physiology phenotype",
                    "Hypermelanotic macule",
                    "Hyperpigmentation of the skin",
                    "increased biological_process in skin of body",
                    "increased pigmentation",
                    "thoracic segment of trunk",
                    "circulatory organ",
                    "heart morphology phenotype",
                    "circulatory organ phenotype",
                    "heart",
                    "thoracic cavity element phenotype",
                    "Irregular hyperpigmentation",
                    "cardiovascular system morphology phenotype",
                    "primary circulatory organ",
                    "viscus phenotype",
                    "heart phenotype",
                    "Abnormality of the cardiovascular system",
                    "superficial fascia",
                    "vascular system",
                    "Abnormality of the vasculature",
                    "vasculature",
                    "pathological entity",
                    "pathological anatomical entity",
                    "U-shaped anatomical entity",
                    "hemorrhage and non-specified extravasation",
                    "ecchymosis",
                    "Abnormal conjugate eye movement",
                    "circulatory disorder",
                    "anatomical cluster",
                    "Abnormality of thumb phalanx",
                    "decreased qualitatively system process",
                    "manual digitopodium bone",
                    "eye physiology phenotype",
                    "digitopodium bone",
                    "manual digit 1 digitopodial skeleton",
                    "manual digit phalanx endochondral element",
                    "autopod bone",
                    "skeleton of manual acropodium",
                    "manual digit digitopodial skeleton",
                    "autopod endochondral element",
                    "Abnormal finger phalanx morphology",
                    "Duplication of thumb phalanx",
                    "Duplication of hand bones",
                    "Complete duplication of phalanx of hand",
                    "multicellular organismal process",
                    "thoracic segment organ phenotype",
                    "Abnormal skull morphology",
                    "Abnormality of skull size",
                    "manual digit 1 phalanx endochondral element",
                    "anatomical conduit phenotype",
                    "axial skeleton plus cranial skeleton",
                    "postcranial axial skeletal system",
                    "skull",
                    "axial skeletal system",
                    "central nervous system",
                    "Aplasia/Hypoplasia of the cerebrum",
                    "regional part of nervous system",
                    "anatomical conduit",
                    "regional part of brain",
                    "skull phenotype",
                    "localised lateral structure",
                    "Abnormal brain morphology",
                    "decreased functionality of the multicellular anatomical structure",
                    "manus bone",
                    "manual digit bone",
                    "forebrain morphology phenotype",
                    "central nervous system morphology phenotype",
                    "brain",
                    "Anemia",
                    "telencephalon",
                    "Abnormal cerebral morphology",
                    "nervous system morphology phenotype",
                    "brain phenotype",
                    "epithelial tube",
                    "epithelial tube phenotype",
                    "neural tube phenotype",
                    "Abnormal nervous system morphology",
                    "anterior neural tube phenotype",
                    "telencephalon phenotype",
                    "obsolete cell",
                    "biological regulation phenotype",
                    "Chromosomal breakage induced by crosslinking agents",
                    "homeostatic process phenotype",
                    "negative regulation of macromolecule biosynthetic process",
                    "cellular process",
                    "cellular process phenotype",
                    "Abnormal cellular phenotype",
                    "Abnormal cellular physiology",
                    "gene expression phenotype",
                    "regulation of cellular process",
                    "biosynthetic process",
                    "macromolecule metabolic process",
                    "decreased qualitatively sensory perception of mechanical stimulus",
                    "decreased functionality of the gonad",
                    "Chromosome breakage",
                    "biological regulation",
                    "biosynthetic process phenotype",
                    "Abnormality of chromosome stability",
                    "negative regulation of macromolecule metabolic process",
                    "Abnormality of metabolism/homeostasis",
                    "regulation of macromolecule metabolic process",
                    "regulation of biosynthetic process",
                    "negative regulation of metabolic process",
                    "material anatomical entity physiology phenotype",
                    "Neurodevelopmental delay",
                    "Abnormality of the nervous system",
                    "forebrain phenotype",
                    "nervous system physiology phenotype",
                    "Global developmental delay",
                    "nervous system process",
                    "Abnormal nervous system physiology",
                    "cardiovascular system phenotype",
                    "telencephalon morphology phenotype",
                    "anatomical system physiology phenotype",
                    "anatomical structure physiology phenotype",
                    "anatomical structure mass phenotype",
                    "Growth abnormality",
                    "multicellular anatomical structure mass phenotype",
                    "anterior neural tube",
                    "decreased material anatomical entity mass",
                    "Abnormality of body weight",
                    "postcranial axial skeleton",
                    "multicellular organism mass phenotype",
                    "Decreased anatomical entity mass",
                    "growth",
                    "Abnormality of the head",
                    "negative regulation of cellular process",
                    "material anatomical entity mass phenotype",
                    "decreased multicellular anatomical structure mass",
                    "localised abdominal segment element",
                    "Decreased body weight",
                    "head",
                    "pre-chordal neural plate",
                    "Eumetazoa",
                    "immature eye",
                    "root",
                    "gastrula morphology phenotype",
                    "multicellular organismal process phenotype",
                    "gastrula",
                    "epithelium",
                    "entire sense organ system",
                    "Subcutaneous hemorrhage",
                    "Microphthalmia",
                    "craniocervical region morphology phenotype",
                    "unilaminar epithelium phenotype",
                    "ectoderm",
                    "decreased qualitatively sensory perception",
                    "neural plate",
                    "negative regulation of gene expression",
                    "future central nervous system phenotype",
                    "head phenotype",
                    "optic cup",
                    "sensory system",
                    "epithelium phenotype",
                    "eye primordium phenotype",
                    "immature eye phenotype",
                    "Abnormal eye morphology",
                    "Abnormality of skin pigmentation",
                    "future central nervous system",
                    "cellular response to stimulus",
                    "decreased size of the organ",
                    "localised kidney",
                    "craniocervical region",
                    "Neoplasm by anatomical site",
                    "ecto-epithelium",
                    "heart plus pericardium",
                    "optic vesicle",
                    "presumptive ectoderm phenotype",
                    "camera-type eye phenotype",
                    "Eukaryota",
                    "vision/eye phenotype",
                    "aplasia or hypoplasia of eyeball of camera-type eye",
                    "presumptive ectoderm",
                    "sensory perception",
                    "future nervous system",
                    "camera-type eye morphology phenotype",
                    "Abnormality of globe size",
                    "regional part of nervous system phenotype",
                    "face phenotype",
                    "head morphology phenotype",
                    "brain morphology phenotype",
                    "visual system",
                    "thoracic segment organ",
                    "multi-tissue structure",
                    "metabolic process",
                    "primordium phenotype",
                    "structure with developmental contribution from neural crest phenotype",
                    "Duplicated collecting system",
                    "sense organ phenotype",
                    "cardiovascular system",
                    "eye phenotype",
                    "neural plate morphology phenotype",
                    "face",
                    "localised compound organ",
                    "anlage",
                    "sense organ",
                    "eye primordium",
                    "eyeball of camera-type eye phenotype",
                    "negative regulation of biosynthetic process",
                    "decreased size of the sense organ",
                    "anatomical entity mass phenotype",
                    "aplastic manual digit 1",
                    "absent organism subdivision in the multicellular organism",
                    "Metazoa",
                    "absent manual digit",
                    "absent digit",
                    "Finger aplasia",
                    "Abnormal reticulocyte morphology",
                    "vestibulo-auditory system",
                    "Strabismus",
                    "erythrocyte morphology phenotype",
                    "Vascular skin abnormality",
                    "reticulocyte",
                    "Abnormal erythrocyte morphology",
                    "digit",
                    "aplasia or hypoplasia of telencephalon",
                    "manual digit plus metapodial segment",
                    "embryonic autopod plate morphology phenotype",
                    "Abnormality of the hand",
                    "anatomical entity length phenotype",
                    "negative regulation of biological process",
                    "decreased length of digit",
                    "decreased size of the material anatomical entity",
                    "Aplasia/hypoplasia involving bones of the hand",
                    "decreased size of the anatomical structure in the pectoral complex",
                    "decreased length of digit 1",
                    "decreased size of the autopodial extension",
                    "manual digit 1 morphology phenotype",
                    "manual digitopodium region",
                    "decreased height of the anatomical entity",
                    "reproductive system physiology phenotype",
                    "regulation of metabolic process",
                    "aplasia or hypoplasia of manual digit 1",
                    "ear phenotype",
                    "autopod region phenotype",
                    "neural tube",
                    "acropodium region",
                    "tube",
                    "cranial skeletal system phenotype",
                    "digitopodium region",
                    "Intellectual disability",
                    "Small for gestational age",
                    "segment of manus",
                    "aplasia or hypoplasia of manual digit",
                    "glandular system",
                    "decreased length of digit 1 or 5",
                    "paired limb/fin segment",
                    "Puberty and gonadal disorders",
                    "decreased number of anatomical entity",
                    "digit 1 phenotype",
                    "developing anatomical structure",
                    "phenotypic effect",
                    "aplasia or hypoplasia of radius bone",
                    "Opisthokonta",
                    "embryo morphology phenotype",
                    "paired limb/fin segment phenotype",
                    "abdomen element",
                    "external genitalia",
                    "sensory perception phenotype",
                    "anatomical entity morphology in the pectoral complex phenotype",
                    "body part movement",
                    "reproductive organ phenotype",
                    "number of platelet phenotype",
                    "macromolecule metabolic process phenotype",
                    "organ",
                    "optic vesicle phenotype",
                    "localised testis",
                    "external genitalia phenotype",
                    "cognition",
                    "Morphological central nervous system abnormality",
                    "male organism",
                    "male reproductive system",
                    "localised anatomical structure",
                    "localised reproductive structure",
                    "cellular organisms",
                    "testis",
                    "increased qualitatively biological_process",
                    "Abnormal reproductive system morphology",
                    "Abnormal testis morphology",
                    "sense organ physiology phenotype",
                    "gonad",
                    "external male genitalia",
                    "localised anatomical entity",
                    "anucleate cell",
                    "absent anatomical structure in the multicellular organism",
                    "Generalized abnormality of skin",
                    "absent mesoderm-derived structure in the multicellular organism",
                    "reproductive system phenotype",
                    "Aplasia/hypoplasia involving the skeleton",
                    "location of anatomical entity phenotype",
                    "decreased functionality of the anatomical structure",
                    "absent anatomical entity in the renal system",
                    "absent limb endochondral element in the forelimb",
                    "germ layer",
                    "manual digit 1",
                    "bone cell",
                    "skeletal element",
                    "absent autopodial extension",
                    "lateral plate mesoderm",
                    "individual digit of digitopodial skeleton",
                    "aplastic anatomical entity",
                    "pectoral appendage skeleton",
                    "integument phenotype",
                    "number of myeloid cell phenotype",
                    "Abnormality of the genital system",
                    "Abnormal bone marrow cell morphology",
                    "camera-type eye",
                    "absent mesoderm-derived structure",
                    "integumental system phenotype",
                    "phalanx endochondral element",
                    "skeletal system",
                    "skin of body",
                    "Abnormality of the eye",
                    "Abnormality of the kidney",
                    "absent anatomical structure in the renal system",
                    "skin of body phenotype",
                    "ectoderm-derived structure",
                    "absent abdominal segment element",
                    "structure with developmental contribution from neural crest",
                    "decreased length of manual digit 1",
                    "skin of body morphology phenotype",
                    "absent radius bone",
                    "decreased number of anatomical structure",
                    "decreased number of myeloid cell",
                    "sensory system phenotype",
                    "neutrophil",
                    "Abnormality of the immune system",
                    "pathological phenotype observation",
                    "hematopoietic system",
                    "Phenotypic abnormality",
                    "limb skeleton subdivision",
                    "Abnormal leukocyte count",
                    "reproductive structure phenotype",
                    "material anatomical entity",
                    "number of anatomical enitites of type skeletal element phenotype",
                    "circulatory system",
                    "autopod region",
                    "nucleic acid metabolic process",
                    "number of leukocyte phenotype",
                    "Decreased total neutrophil count",
                    "Aplasia/Hypoplasia of the radius",
                    "germ layer / neural crest phenotype",
                    "musculature phenotype",
                    "immune system",
                    "forelimb bud morphology phenotype",
                    "localised gonad",
                    "myeloid leukocyte phenotype",
                    "hematopoietic system phenotype",
                    "regulation of biological process",
                    "optic cup morphology phenotype",
                    "Abnormality of the skeletal system",
                    "kidney morphology phenotype",
                    "immune system phenotype",
                    "unilaminar epithelium",
                    "digit 1 or 5 phenotype",
                    "cellular response to stress phenotype",
                    "Pancytopenia",
                    "arm bone",
                    "granulocyte",
                    "Abnormal leukocyte morphology",
                    "Bruising susceptibility",
                    "blood cell",
                    "visual system phenotype",
                    "decreased number of material anatomical entity",
                    "nervous system phenotype",
                    "platelet",
                    "myeloid cell",
                    "Absent radius",
                    "phalanx",
                    "cell phenotype",
                    "paired limb/fin bud phenotype",
                    "eukaryotic cell",
                    "craniocervical region phenotype",
                    "compound organ phenotype",
                    "upper limb segment phenotype",
                    "blood cell phenotype",
                    "system process",
                    "number of anatomical enitites of type anatomical structure phenotype",
                    "endocrine system",
                    "hemolymphoid system",
                    "absent abdomen element in the renal system",
                    "Macule",
                    "organ system subdivision",
                    "musculoskeletal system phenotype",
                    "aplasia or hypoplasia of anatomical entity",
                    "skeleton of digitopodium",
                    "cranial skeletal system",
                    "appendicular skeleton",
                    "absent anatomical structure",
                    "pigmentation",
                    "testis phenotype",
                    "absent multicellular anatomical structure in the tissue",
                    "absent limb bone",
                    "upper urinary tract",
                    "shape of continuant phenotype",
                    "absent long bone in the forelimb",
                    "interphase",
                    "absent arm bone in the forelimb",
                    "manus morphology phenotype",
                    "Abnormality of the musculoskeletal system",
                    "musculoskeletal system",
                    "Leukemia",
                    "absent multicellular anatomical structure in the renal system",
                    "main body axis",
                    "Aplasia/Hypoplasia involving the central nervous system",
                    "absent limb bone in the forelimb",
                    "anatomical structure phenotype",
                    "absent bone of pectoral complex",
                    "size of multicellular organism phenotype",
                    "male organism phenotype",
                    "neutrophil phenotype",
                    "oxygen accumulating cell",
                    "Abnormality of the skin",
                    "forelimb bone",
                    "immune system morphology phenotype",
                    "multicellular organism height phenotype",
                    "subdivision of head",
                    "All",
                    "shape of kidney phenotype",
                    "absent organ in the renal system",
                    "mesoderm phenotype",
                    "absent material anatomical entity in the limb",
                    "number of anatomical enitites of type multicellular anatomical structure phenotype",
                    "decreased number of reticulocyte",
                    "absent long bone",
                    "segment of autopod",
                    "material anatomical entity phenotype",
                    "number of anatomical enitites of type lateral structure phenotype",
                    "behavior",
                    "number of cell phenotype",
                    "craniofacial/craniocervical phenotype",
                    "agenesis of anatomical entity",
                    "trunk region element",
                    "decreased qualitatively nervous system process",
                    "eye movement phenotype",
                    "paired limb/fin",
                    "pre-chordal neural plate phenotype",
                    "leukocyte morphology phenotype",
                    "number of anatomical enitites of type trunk region element phenotype",
                    "manual digit 1 phalanx",
                    "reproductive system",
                    "absent anatomical entity in the tissue",
                    "tube phenotype",
                    "erythrocyte",
                    "Cafe-au-lait spot",
                    "number of anatomical enitites of type organism subdivision phenotype",
                    "musculature of body",
                    "skeleton phenotype",
                    "decreased size of the eyeball of camera-type eye",
                    "granulocyte morphology phenotype",
                    "G2 phase",
                    "Microcephaly",
                    "absent compound organ in the renal system",
                    "Aplasia/hypoplasia involving bones of the extremities",
                    "skeleton of manual digitopodium",
                    "serotonin secreting cell",
                    "abdominal segment element",
                    "absent organism subdivision",
                    "erythroid lineage cell morphology phenotype",
                    "number of hematopoietic cell phenotype",
                    "organism subdivision",
                    "Abnormality of the male genitalia",
                    "absent multicellular anatomical structure",
                    "Short digit",
                    "number of anatomical enitites of type material anatomical entity phenotype",
                    "absent anatomical entity",
                    "pigmentation phenotype",
                    "size of anatomical entity phenotype",
                    "neurectoderm phenotype",
                    "male reproductive organ phenotype",
                    "increased pigmentation in skin of body",
                    "radius bone phenotype",
                    "appendicular skeletal system",
                    "body proper",
                    "absent forelimb long bone",
                    "gonad phenotype",
                    "decreased system process",
                    "neoplasm phenotype",
                    "biogenic amine secreting cell",
                    "absent trunk region element in the renal system",
                    "upper urinary tract phenotype",
                    "absent abdomen element",
                    "decreased functionality of the material anatomical entity",
                    "absent endochondral element in the forelimb",
                    "absent cavitated compound organ in the renal system",
                    "simple eye phenotype",
                    "multicellular organism phenotype",
                    "absent abdominal segment element in the renal system",
                    "limb bud",
                    "number of anatomical enitites of type kidney phenotype",
                    "Abnormal skin morphology",
                    "external male genitalia phenotype",
                    "subdivision of organism along main body axis phenotype",
                    "Abnormality of the upper urinary tract",
                    "number of anatomical enitites of type granulocyte phenotype",
                    "secretory cell",
                    "lateral structure phenotype",
                    "absent bone element in the forelimb",
                    "taxon specific phenotype",
                    "multicellular organism",
                    "number of anatomical enitites of type endochondral bone phenotype",
                    "abdominal segment element phenotype",
                    "Prolonged G2 phase of cell cycle",
                    "thoracic cavity element",
                    "anatomical entity phenotype",
                    "absent anatomical entity in the skeletal system",
                    "multi-limb segment region",
                    "Aplasia/Hypoplasia affecting the eye",
                    "multicellular anatomical structure phenotype",
                    "absent forelimb endochondral element",
                    "Abnormal total neutrophil count",
                    "male reproductive system phenotype",
                    "response to stress phenotype",
                    "number of anatomical enitites of type abdomen element phenotype",
                    "vestibulo-auditory system phenotype",
                    "renal system",
                    "cell",
                    "abdomen",
                    "decreased size of the digit",
                    "surface structure phenotype",
                    "anatomical entity morphology in the manus phenotype",
                    "decreased sensory perception",
                    "absent organ",
                    "Abnormal hand morphology",
                    "localised male reproductive organ",
                    "localised abdomen element",
                    "occurrent",
                    "limb morphology phenotype",
                    "absent kidney",
                    "absent multicellular anatomical structure in the skeletal system",
                    "kinesthetic behavior",
                    "Aplasia involving forearm bones",
                    "Thrombocytopenia",
                    "Duplication of phalanx of hand",
                    "metabolic process phenotype",
                    "phenotype",
                    "independent continuant",
                    "Abnormal myeloid leukocyte morphology",
                    "size of skull phenotype",
                    "growth phenotype",
                    "absent lateral structure in the renal system",
                    "ectoderm morphology phenotype",
                    "manus",
                    "renal system phenotype",
                    "circulatory system phenotype",
                    "absent anatomical structure in the limb",
                    "Abnormality of mental function",
                    "localised organ",
                    "number of anatomical enitites of type organ phenotype",
                    "forelimb zeugopod skeleton",
                    "absent limb endochondral element in the limb",
                    "anatomical entity dysfunction in independent continuant",
                    "paired limb/fin phenotype",
                    "localised reproductive organ",
                    "number of anatomical enitites of type compound organ phenotype",
                    "excretory system",
                    "decreased qualitatively biological_process",
                    "endochondral element",
                    "number of anatomical enitites of type cavitated compound organ phenotype",
                    "forelimb phenotype",
                    "ectoderm phenotype",
                    "subdivision of trunk",
                    "trunk",
                    "Abnormal forebrain morphology",
                    "absent endochondral bone",
                    "Abnormal renal morphology",
                    "cell cycle phenotype",
                    "forelimb zeugopod phenotype",
                    "limb endochondral element phenotype",
                    "absent trunk region element",
                    "subdivision of head phenotype",
                    "anterior region of body",
                    "absent trunk region element in the multicellular organism",
                    "absent material anatomical entity in the renal system",
                    "digit 1 digitopodial skeleton",
                    "tissue",
                    "absent material anatomical entity",
                    "material entity",
                    "entity",
                    "decreased number of leukocyte",
                    "cavitated compound organ",
                    "manual digit phenotype",
                    "Abnormality of the urinary system",
                    "integument",
                    "forelimb zeugopod bone morphology phenotype",
                    "Renal hypoplasia/aplasia",
                    "kidney phenotype",
                    "compound organ",
                    "Cryptorchidism",
                    "organ system subdivision phenotype",
                    "lateral plate mesoderm morphology phenotype",
                    "absent endochondral bone in the limb",
                    "autopod region morphology phenotype",
                    "nucleate cell",
                    "subdivision of trunk phenotype",
                    "process",
                    "multicellular anatomical structure",
                    "biological phase",
                    "number of anatomical enitites of type anatomical entity phenotype",
                    "negative regulation of gene expression phenotype",
                    "trunk region element phenotype",
                    "mesoderm-derived structure phenotype",
                    "system process phenotype",
                    "enucleated reticulocyte",
                    "bone of appendage girdle complex",
                    "Abnormal granulocyte count",
                    "aplasia or hypoplasia of skeleton",
                    "number of anatomical enitites of type neutrophil phenotype",
                    "Hematological neoplasm",
                    "localised multicellular anatomical structure",
                    "multicellular organism morphology phenotype",
                    "3-D shape anatomical entity",
                    "DNA metabolic process",
                    "continuant",
                    "multi-tissue structure phenotype",
                    "Abnormal cellular immune system morphology",
                    "Renal agenesis",
                    "cavitated compound organ phenotype",
                    "anatomical structure",
                    "absent forelimb endochondral element in the forelimb",
                    "Abnormality of the integument",
                    "appendage phenotype",
                    "Abnormal ear physiology",
                    "Abnormal granulocyte morphology",
                    "Abnormality of the genitourinary system",
                    "biological_process phenotype",
                    "renal/urinary system phenotype",
                    "male reproductive organ",
                    "absent anatomical entity in the multicellular organism",
                    "absent multicellular anatomical structure in the multicellular organism",
                    "anatomical entity morphology phenotype",
                    "programmed DNA elimination by chromosome breakage",
                    "absent organ in the multicellular organism",
                    "neural tube morphology phenotype",
                    "bone of pectoral complex morphology phenotype",
                    "Abnormality of neutrophils",
                    "genitourinary system",
                    "limb long bone phenotype",
                    "organism subdivision phenotype",
                    "Abnormal external genitalia morphology",
                    "anatomical collection phenotype",
                    "viscus",
                    "primordium",
                    "localised material anatomical entity",
                    "anatomical system",
                    "motile cell",
                    "long bone morphology phenotype",
                    "limb long bone",
                    "ear",
                    "Abnormality of the ear",
                    "bone of appendage girdle complex phenotype",
                    "absent compound organ",
                    "increased biological_process",
                    "Abnormal male external genitalia morphology",
                    "endochondral bone phenotype",
                    "digit morphology phenotype",
                    "bone marrow cell",
                    "lateral structure",
                    "Abnormality of multiple cell lineages in the bone marrow",
                    "disconnected anatomical group",
                    "absent endochondral element in the limb",
                    "decreased number of hematopoietic cell",
                    "non-connected functional system",
                    "behavior process phenotype",
                    "forelimb long bone",
                    "skull morphology phenotype",
                    "programmed DNA elimination",
                    "orbital region",
                    "hematopoietic cell",
                    "decreased number of granulocyte",
                    "forelimb bone phenotype",
                    "number of anatomical enitites of type reticulocyte phenotype",
                    "kidney",
                    "zeugopodial skeleton",
                    "anatomical system phenotype",
                    "zeugopod",
                    "decreased number of neutrophil",
                    "biological_process",
                    "multi-limb segment region phenotype",
                    "absent forelimb zeugopod bone",
                    "skeletal system morphology phenotype",
                    "absent bone of free limb or fin",
                    "orbital region phenotype",
                    "Abnormality of the upper limb",
                    "skeleton",
                    "non-material anatomical boundary",
                    "skeletal element phenotype",
                    "presumptive structure phenotype",
                    "abdominal segment of trunk",
                    "absent bone element",
                    "absent material anatomical entity in the limb bud",
                    "Abnormal skeletal morphology",
                    "leukocyte",
                    "absent bone of appendage girdle complex in the forelimb",
                    "appendicular skeleton phenotype",
                    "decreased qualitatively multicellular organismal process",
                    "immaterial anatomical entity",
                    "neural plate phenotype",
                    "absent bone of pectoral complex in the limb",
                    "absent anatomical structure in the skeletal system",
                    "Localized skin lesion",
                    "embryo",
                    "blastula",
                    "skeletal system phenotype",
                    "limb skeleton subdivision phenotype",
                    "bone of free limb or fin phenotype",
                    "paired limb/fin skeleton phenotype",
                    "absent multicellular anatomical structure in the limb",
                    "absent bone element in the limb",
                    "size of eyeball of camera-type eye phenotype",
                    "absent skeletal element in the forelimb",
                    "embryo phenotype",
                    "decreased length of organism subdivision",
                    "absent lateral structure",
                    "Abnormal immune system morphology",
                    "forelimb skeleton phenotype",
                    "anatomical cluster phenotype",
                    "integumental system",
                    "ectoderm-derived structure phenotype",
                    "anatomical entity morphology in the skeleton of pectoral complex phenotype",
                    "absent anatomical structure in the forelimb",
                    "regional part of brain phenotype",
                    "regulation of gene expression",
                    "absent radius endochondral element",
                    "absent forelimb zeugopod bone in the forelimb",
                    "surface structure",
                    "forelimb bud",
                    "absent mesoderm-derived structure in the forelimb",
                    "paired limb/fin skeleton",
                    "Aplasia/Hypoplasia of fingers",
                    "germ layer phenotype",
                    "decreased size of the organism subdivision",
                    "gene expression",
                    "Abnormal morphology of the radius",
                    "abdomen element phenotype",
                    "limb segment phenotype",
                    "endochondral element phenotype",
                    "decreased number of cell",
                    "absent organ in the limb",
                    "absent anatomical entity in the limb bud",
                    "bone of pectoral complex phenotype",
                    "Abnormal upper limb bone morphology",
                    "anatomical entity",
                    "embryonic structure",
                    "limb phenotype",
                    "endochondral bone",
                    "long bone",
                    "limb segment",
                    "Abnormality of limb bone",
                    "U-shaped kidney",
                    "limb endochondral element",
                    "decreased anatomical structure mass",
                    "paired limb/fin bud",
                    "arm",
                    "Abnormal cardiovascular system morphology",
                    "trunk phenotype",
                    "absent organ in the tissue",
                    "pectoral appendage bud phenotype",
                    "number of anatomical enitites of type endochondral element phenotype",
                    "myeloid leukocyte",
                    "dense mesenchyme tissue",
                    "skeleton of limb",
                    "Hypogonadism",
                    "long bone phenotype",
                    "limb bud phenotype",
                    "Aplasia/hypoplasia involving bones of the upper limbs",
                    "number of anatomical enitites of type bone element phenotype",
                    "ecto-epithelium phenotype",
                    "face morphology phenotype",
                    "autopodial extension",
                    "appendage",
                    "vasculature phenotype",
                    "absent forelimb endochondral element in the limb",
                    "enucleated reticulocyte morphology phenotype",
                    "absent bone of free limb or fin in the forelimb",
                    "lateral plate mesoderm phenotype",
                    "sensory perception of sound phenotype",
                    "absent multicellular anatomical structure in the forelimb",
                    "absent bone of appendage girdle complex",
                    "subdivision of organism along main body axis",
                    "germ layer morphology phenotype",
                    "absent bone of free limb or fin in the limb",
                    "Complete duplication of thumb phalanx",
                    "number of anatomical enitites of type mesoderm-derived structure phenotype",
                    "decreased length of anatomical entity",
                    "absent radius endochondral element in the forelimb",
                    "Abnormality of thrombocytes",
                    "absent limb bone in the limb",
                    "eyeball of camera-type eye",
                    "Abnormal thumb morphology",
                    "forelimb zeugopod morphology phenotype",
                    "Abnormal appendicular skeleton morphology",
                    "primary circulatory organ phenotype",
                    "Pallor",
                    "aplastic forelimb zeugopod bone",
                    "absent forelimb bone in the limb",
                    "decreased size of the ectoderm-derived structure",
                    "anatomical collection",
                    "pectoral complex",
                    "pectoral appendage",
                    "limb",
                    "erythroid lineage cell",
                    "radius bone morphology phenotype",
                    "mesoderm-derived structure",
                    "forelimb skeleton",
                    "Abnormality of the endocrine system",
                    "reproductive structure",
                    "platelet phenotype",
                    "zeugopod phenotype",
                    "developing anatomical structure phenotype",
                    "musculature of body phenotype",
                    "delayed growth",
                    "digit 1",
                    "arm phenotype",
                    "camera-type eye physiology phenotype",
                    "bone of pectoral complex",
                    "decreased size of the manual digit",
                    "bone of free limb or fin",
                    "Abnormality of head or neck",
                    "limb bone",
                    "Anemic pallor",
                    "forelimb endochondral element",
                    "number of anatomical enitites of type abdominal segment element phenotype",
                    "embryonic tissue phenotype",
                    "subdivision of skeleton phenotype",
                    "skeleton of limb phenotype",
                    "forelimb bud phenotype",
                    "genitourinary system phenotype",
                    "absent forelimb bone",
                    "presumptive structure",
                    "simple eye",
                    "germ layer / neural crest",
                    "subdivision of skeletal system",
                    "renal collecting system phenotype",
                    "appendage girdle complex",
                    "subdivision of skeletal system phenotype",
                    "forebrain",
                    "absent anatomical entity in the forelimb",
                    "neurectoderm",
                    "Abnormal limb bone morphology",
                    "Neoplasm",
                    "absent forelimb bone in the forelimb",
                    "absent anatomical structure in the tissue",
                    "bone marrow",
                    "absent material anatomical entity in the tissue",
                    "absent arm bone",
                    "DNA damage response phenotype",
                    "mesenchyme phenotype",
                    "Neurodevelopmental abnormality",
                    "Abnormal forearm morphology",
                    "system",
                    "limb bone phenotype",
                    "forelimb endochondral element phenotype",
                    "phalanx of manus",
                    "limb bone morphology phenotype",
                    "forelimb zeugopod",
                    "eye movement",
                    "radius endochondral element",
                    "Abnormal localization of kidney",
                    "Abnormal heart morphology",
                    "absent mesoderm-derived structure in the limb",
                    "acropodial skeleton",
                    "limb long bone morphology phenotype",
                    "Aplasia/hypoplasia involving forearm bones",
                    "musculature",
                    "Abnormal axial skeleton morphology",
                    "subdivision of skeleton",
                    "skeleton of pectoral complex",
                    "radius bone",
                    "bone element",
                    "subdivision of organism along appendicular axis",
                    "forelimb zeugopod bone",
                    "Duplication of bones involving the upper extremities",
                    "decreased size of the multicellular anatomical structure",
                    "mesoderm morphology phenotype",
                    "nervous system",
                    "absent endochondral element",
                    "Abnormality of body height",
                    "digit phenotype",
                    "bone element phenotype",
                    "behavior phenotype",
                    "absent bone of pectoral complex in the forelimb",
                    "embryonic structure phenotype",
                    "Absent thumb",
                    "absent endochondral bone in the forelimb",
                    "behavior process",
                    "central nervous system phenotype",
                    "Reticulocytopenia",
                    "pectoral appendage bud",
                    "macromolecule biosynthetic process",
                    "mesoderm",
                    "Abnormal forearm bone morphology",
                    "forelimb",
                    "absent material anatomical entity in the forelimb",
                    "absent limb long bone",
                    "appendicular skeleton morphology phenotype",
                    "absent skeletal element",
                    "biological_process rate phenotype",
                    "anatomical entity morphology in the appendage girdle complex phenotype",
                    "renal system morphology phenotype",
                    "forelimb long bone phenotype",
                    "manus phenotype",
                    "renal collecting system",
                    "dense mesenchyme tissue phenotype",
                    "Abnormal bleeding",
                    "forelimb zeugopod bone phenotype",
                    "Hearing abnormality",
                    "embryonic tissue",
                    "decreased length of manual digit",
                    "mesenchyme",
                    "reproductive organ",
                    "pectoral appendage skeleton phenotype",
                    "Aplasia/hypoplasia of the extremities",
                    "absent skeletal element in the limb",
                    "embryonic tissue morphology phenotype",
                    "Decreased multicellular organism mass",
                    "absent organ in the forelimb",
                    "regulation of macromolecule biosynthetic process",
                    "decreased size of the anatomical entity in the pectoral complex",
                    "absent limb long bone in the forelimb",
                    "absent bone of appendage girdle complex in the limb",
                    "limb bud morphology phenotype",
                    "homeostatic process",
                    "absent material anatomical entity in the skeletal system",
                    "absent cavitated compound organ",
                    "arm bone phenotype",
                    "Abnormality of limbs",
                    "forelimb morphology phenotype",
                    "mesenchyme morphology phenotype",
                    "decreased number of platelet",
                    "Abnormal platelet morphology",
                    "Abnormal platelet count",
                    "Absent forearm bone",
                    "digit 1 plus metapodial segment",
                    "anatomical line",
                    "eye",
                    "absent limb endochondral element",
                    "decreased length of material anatomical entity",
                    "decreased length of manual digit 1 or 5",
                    "autopodial extension phenotype",
                    "pectoral appendage phenotype",
                    "Abnormal finger morphology",
                    "decreased size of the material anatomical entity in the pectoral complex",
                    "decreased length of multicellular anatomical structure",
                    "Abnormality of blood and blood-forming tissues",
                    "Aplasia/Hypoplasia of the thumb",
                    "decreased length of autopodial extension",
                    "upper limb segment",
                    "manual digit 1 plus metapodial segment",
                    "skeleton of manus",
                    "decreased size of the anatomical structure",
                    "absent anatomical entity in the limb",
                    "manual digit",
                    "absent material anatomical entity in the multicellular organism",
                    "digit 1 or 5",
                    "macromolecule biosynthetic process phenotype",
                    "autopodial skeleton",
                    "decreased size of the anatomical entity",
                    "decreased size of the multicellular anatomical structure in the pectoral complex",
                    "programmed DNA elimination by chromosome breakage phenotype",
                    "anatomical entity physiology phenotype",
                    "decreased length of anatomical structure",
                    "absent forelimb long bone in the forelimb",
                    "digit plus metapodial segment",
                    "Decreased head circumference",
                    "tissue phenotype",
                    "Short finger",
                    "sensory perception of mechanical stimulus phenotype",
                    "Short thumb",
                    "manual digit morphology in the manus phenotype",
                    "Abnormal digit morphology",
                    "embryonic autopod plate",
                    "organ phenotype",
                    "subdivision of organism along appendicular axis phenotype",
                    "manual digit 1 or 5",
                ],
                "has_phenotype_count": 32,
                "score": None,
                "exact_synonyms": [
                    "FACE|FANCE|FANCE Fanconi anaemia|FANCE Fanconi anemia|Fanconi Anemia, complementation group type E|Fanconi anaemia caused by mutation in FANCE|Fanconi anaemia complementation group type E|Fanconi anemia caused by mutation in FANCE|Fanconi anemia complementation group E|Fanconi anemia complementation group type E|face"
                ],
                "related_synonyms": ["Fanconi anemia, complementation group E"],
                "highlighting": None,
            },
            {
                "id": "MONDO:0044325",
                "category": "biolink:Disease",
                "name": "Fanconi anemia, complementation group W",
                "full_name": None,
                "deprecated": None,
                "description": None,
                "xref": ["DOID:0060978", "MEDGEN:1621245", "OMIM:617784", "UMLS:C4521564"],
                "provided_by": "phenio_nodes",
                "in_taxon": None,
                "in_taxon_label": None,
                "symbol": None,
                "synonym": ["FANCW", "Fanconi anemia, complementation group W"],
                "broad_synonym": None,
                "exact_synonym": None,
                "narrow_synonym": None,
                "related_synonym": None,
                "subsets": ["gard_rare", "nord_rare", "otar", "rare"],
                "uri": None,
                "iri": None,
                "namespace": "MONDO",
                "has_phenotype": [
                    "HP:0002247",
                    "HP:0002984",
                    "HP:0002863",
                    "HP:0001510",
                    "HP:0001511",
                    "HP:0002119",
                    "HP:0009777",
                    "HP:0001748",
                    "HP:0000824",
                    "HP:0002518",
                    "HP:0002308",
                    "HP:0031689",
                    "HP:0011800",
                    "HP:0000089",
                    "HP:0000252",
                    "HP:0410049",
                ],
                "has_phenotype_label": [
                    "Duodenal atresia",
                    "Hypoplasia of the radius",
                    "Myelodysplasia",
                    "Growth delay",
                    "Intrauterine growth retardation",
                    "Ventriculomegaly",
                    "Absent thumb",
                    "Polysplenia",
                    "Decreased response to growth hormone stimulation test",
                    "Abnormal periventricular white matter morphology",
                    "Chiari malformation",
                    "Megakaryocyte dysplasia",
                    "Midface retrusion",
                    "Renal hypoplasia",
                    "Microcephaly",
                    "Abnormal radial ray morphology",
                ],
                "has_phenotype_closure": [
                    "HP:0000240",
                    "UPHENO:0075804",
                    "UBERON:0002090",
                    "HP:0009121",
                    "HP:0010935",
                    "HP:0008678",
                    "UBERON:0001008",
                    "UPHENO:0002642",
                    "HP:0000089",
                    "UPHENO:0076779",
                    "UBERON:0004122",
                    "UBERON:8450002",
                    "UPHENO:0087427",
                    "UBERON:0002113",
                    "UBERON:0011143",
                    "UPHENO:3000004",
                    "UBERON:0001444",
                    "HP:0000271",
                    "UBERON:0001456",
                    "UPHENO:0087907",
                    "HP:0000234",
                    "UPHENO:0075998",
                    "HP:0000152",
                    "UPHENO:0002928",
                    "UPHENO:3000000",
                    "HP:0011800",
                    "UPHENO:0086589",
                    "CL:0000000",
                    "UPHENO:0088145",
                    "CL:0000255",
                    "CL:0001035",
                    "CL:0002092",
                    "UBERON:0002371",
                    "UPHENO:0003237",
                    "UBERON:0004733",
                    "UBERON:0001895",
                    "UPHENO:0086932",
                    "UPHENO:0002910",
                    "UPHENO:0003460",
                    "UPHENO:0075948",
                    "UBERON:0002028",
                    "HP:0002308",
                    "UBERON:0003103",
                    "UPHENO:0003936",
                    "HP:0002438",
                    "UBERON:0004732",
                    "UPHENO:0071344",
                    "UBERON:0011138",
                    "UPHENO:0003459",
                    "UBERON:0011299",
                    "UBERON:0003544",
                    "UBERON:0011215",
                    "UBERON:0005162",
                    "UPHENO:0002841",
                    "UPHENO:0074038",
                    "UPHENO:0081562",
                    "HP:0002500",
                    "UPHENO:0074051",
                    "UBERON:0002437",
                    "HP:0002060",
                    "UPHENO:0073911",
                    "UPHENO:0002874",
                    "UBERON:0001869",
                    "UPHENO:0003030",
                    "UPHENO:0076799",
                    "UPHENO:0073886",
                    "UPHENO:0081210",
                    "UPHENO:0087531",
                    "UPHENO:0002570",
                    "HP:0010993",
                    "HP:0002352",
                    "UPHENO:0050065",
                    "UPHENO:0005506",
                    "UPHENO:0087472",
                    "UPHENO:0080588",
                    "UBERON:0001890",
                    "UPHENO:0052245",
                    "UPHENO:0052354",
                    "UPHENO:0005141",
                    "UPHENO:0081601",
                    "HP:0000864",
                    "HP:0000929",
                    "HP:0000818",
                    "HP:0031073",
                    "GO:0002790",
                    "UBERON:0007811",
                    "GO:0046879",
                    "UBERON:0004092",
                    "UBERON:0000481",
                    "UPHENO:0077889",
                    "UPHENO:0002529",
                    "UPHENO:0003236",
                    "UPHENO:0005434",
                    "HP:0000079",
                    "UPHENO:0004615",
                    "HP:0040075",
                    "UPHENO:0087363",
                    "HP:0011747",
                    "UPHENO:0080220",
                    "UPHENO:0005611",
                    "UPHENO:0004618",
                    "UPHENO:0087376",
                    "UPHENO:0002764",
                    "UPHENO:0003186",
                    "NCBITaxon:6072",
                    "NCBITaxon:33208",
                    "UPHENO:0002844",
                    "UPHENO:0005571",
                    "UPHENO:0088065",
                    "UPHENO:0087516",
                    "UPHENO:0074037",
                    "GO:0030252",
                    "GO:0023052",
                    "GO:0006810",
                    "UPHENO:0075772",
                    "UBERON:0015204",
                    "GO:0140352",
                    "GO:0007154",
                    "HP:0000830",
                    "UPHENO:0052180",
                    "UPHENO:0005285",
                    "HP:0000077",
                    "UPHENO:0052226",
                    "UPHENO:0002685",
                    "UPHENO:0005470",
                    "UPHENO:0052678",
                    "UPHENO:0002267",
                    "UPHENO:0049691",
                    "UPHENO:0002579",
                    "UPHENO:0077890",
                    "UPHENO:0083952",
                    "UBERON:0003057",
                    "GO:0009914",
                    "GO:0071705",
                    "GO:0051179",
                    "UPHENO:0071339",
                    "UBERON:0002196",
                    "UBERON:0001894",
                    "NCBITaxon:1",
                    "UPHENO:0052518",
                    "UPHENO:0053355",
                    "UPHENO:0003055",
                    "CL:0000763",
                    "UPHENO:0086485",
                    "UBERON:0001049",
                    "UBERON:0003080",
                    "UPHENO:0083951",
                    "UPHENO:0002523",
                    "UPHENO:0049647",
                    "UBERON:0002616",
                    "UPHENO:0005590",
                    "UPHENO:0050014",
                    "UPHENO:0049813",
                    "UBERON:0000483",
                    "UPHENO:0086735",
                    "UPHENO:0002736",
                    "UBERON:0000033",
                    "UBERON:0002530",
                    "UPHENO:0005427",
                    "HP:0012503",
                    "UPHENO:0076812",
                    "UPHENO:0071310",
                    "UBERON:0000454",
                    "UPHENO:0005652",
                    "UPHENO:0005120",
                    "UPHENO:0049890",
                    "UPHENO:0053121",
                    "UBERON:0004734",
                    "UPHENO:0073937",
                    "UBERON:0002368",
                    "UPHENO:0002553",
                    "NCBITaxon:33154",
                    "UPHENO:0005441",
                    "UPHENO:0052867",
                    "NCBITaxon:131567",
                    "UBERON:0002049",
                    "UPHENO:0087267",
                    "UBERON:0005156",
                    "UBERON:0009569",
                    "UPHENO:0002661",
                    "UPHENO:0014351",
                    "UBERON:0034923",
                    "UPHENO:0083689",
                    "UPHENO:0014332",
                    "UPHENO:0003093",
                    "UBERON:0002106",
                    "UBERON:0000916",
                    "HP:0025408",
                    "UPHENO:0087547",
                    "HP:0009799",
                    "HP:0001748",
                    "HP:0002012",
                    "NCBITaxon:2759",
                    "UPHENO:0002819",
                    "UPHENO:0011558",
                    "UBERON:0002465",
                    "UPHENO:0002832",
                    "UPHENO:0002596",
                    "UPHENO:0002576",
                    "UPHENO:0011931",
                    "UPHENO:0011533",
                    "UPHENO:0087123",
                    "UBERON:0003460",
                    "UPHENO:0002861",
                    "UPHENO:0001360",
                    "UBERON:0001423",
                    "UPHENO:0002834",
                    "UBERON:0000383",
                    "UBERON:0004120",
                    "UPHENO:0004888",
                    "HP:0001155",
                    "UBERON:0000075",
                    "HP:0040070",
                    "HP:0009821",
                    "UBERON:0003937",
                    "UPHENO:0082875",
                    "UPHENO:0076740",
                    "UPHENO:0002816",
                    "UBERON:0000007",
                    "UBERON:0015001",
                    "UBERON:0002386",
                    "UPHENO:0002648",
                    "UBERON:0004375",
                    "UPHENO:0053234",
                    "UBERON:0013701",
                    "UBERON:0008962",
                    "UPHENO:0026108",
                    "UBERON:0002204",
                    "UPHENO:0046397",
                    "UPHENO:0069062",
                    "UPHENO:0086172",
                    "UPHENO:0001303",
                    "UBERON:0019261",
                    "UPHENO:0049724",
                    "UPHENO:0011536",
                    "UPHENO:0002650",
                    "UPHENO:0005055",
                    "UBERON:0004357",
                    "UBERON:0010712",
                    "UBERON:0010707",
                    "UPHENO:0068921",
                    "HP:0003026",
                    "UPHENO:0063594",
                    "UPHENO:0088186",
                    "UPHENO:0069266",
                    "UPHENO:0002976",
                    "UPHENO:0003069",
                    "HP:0100763",
                    "HP:0011844",
                    "UPHENO:0009146",
                    "UBERON:0002405",
                    "HP:0001511",
                    "UBERON:0015203",
                    "UPHENO:0087663",
                    "UPHENO:0003088",
                    "UPHENO:0056134",
                    "UPHENO:0068848",
                    "UPHENO:0074228",
                    "UPHENO:0076703",
                    "UBERON:0011584",
                    "UBERON:0002495",
                    "UPHENO:0002525",
                    "UPHENO:0087665",
                    "UPHENO:0005092",
                    "UBERON:0000467",
                    "UPHENO:0008548",
                    "HP:0000119",
                    "UBERON:0002101",
                    "UBERON:0010708",
                    "UPHENO:0004885",
                    "HP:0002597",
                    "HP:0000001",
                    "UPHENO:0046445",
                    "GO:0008150",
                    "UBERON:0011137",
                    "UPHENO:0003177",
                    "UPHENO:0068898",
                    "UPHENO:0002859",
                    "UPHENO:0046392",
                    "UPHENO:0071308",
                    "BFO:0000003",
                    "UPHENO:0076720",
                    "UPHENO:0046505",
                    "UPHENO:0069327",
                    "UPHENO:0069292",
                    "UBERON:0002037",
                    "UPHENO:0002542",
                    "UBERON:0004111",
                    "UPHENO:0056077",
                    "UBERON:0003133",
                    "UPHENO:0005542",
                    "UPHENO:0002870",
                    "UPHENO:0002902",
                    "UPHENO:0002559",
                    "UPHENO:0004519",
                    "UPHENO:0073978",
                    "UBERON:0010316",
                    "UBERON:0004535",
                    "UPHENO:0076754",
                    "UBERON:0001015",
                    "HP:0009815",
                    "UBERON:0000153",
                    "UBERON:0000990",
                    "UPHENO:0052694",
                    "UBERON:0003104",
                    "UPHENO:0005552",
                    "UPHENO:0063563",
                    "GO:0007275",
                    "HP:0000309",
                    "GO:0046903",
                    "UBERON:0004288",
                    "UPHENO:0003799",
                    "UPHENO:0052778",
                    "UPHENO:0046540",
                    "UPHENO:0002725",
                    "UBERON:0003129",
                    "UBERON:0000924",
                    "UPHENO:0002830",
                    "UPHENO:0069328",
                    "UPHENO:0001440",
                    "UBERON:0003061",
                    "UPHENO:9002003",
                    "UBERON:0002102",
                    "UPHENO:0074310",
                    "UPHENO:0002880",
                    "HP:0000118",
                    "UPHENO:0025509",
                    "UPHENO:0046594",
                    "UPHENO:0004484",
                    "UPHENO:0004507",
                    "UPHENO:0076783",
                    "UBERON:0011676",
                    "UBERON:0001434",
                    "UPHENO:0004466",
                    "UPHENO:0011670",
                    "UPHENO:0049871",
                    "UPHENO:0079872",
                    "UPHENO:0071325",
                    "UPHENO:0069047",
                    "UBERON:0015212",
                    "HP:0002518",
                    "UPHENO:0004595",
                    "HP:0011842",
                    "HP:0002118",
                    "UPHENO:0046472",
                    "UPHENO:0002994",
                    "HP:0002984",
                    "UPHENO:0074229",
                    "UPHENO:0075944",
                    "UPHENO:0002577",
                    "HP:0006496",
                    "HP:0012210",
                    "UBERON:0006598",
                    "UPHENO:0002747",
                    "CL:0000556",
                    "UPHENO:0002546",
                    "UPHENO:0011825",
                    "UBERON:0000025",
                    "HP:0033127",
                    "UPHENO:0002731",
                    "UBERON:0000160",
                    "UPHENO:0002988",
                    "HP:0009777",
                    "UPHENO:0080200",
                    "UPHENO:0002586",
                    "HP:0025031",
                    "HP:0007364",
                    "UBERON:0004381",
                    "HP:0005561",
                    "GO:0009987",
                    "UBERON:0005291",
                    "UPHENO:0063565",
                    "UPHENO:0003163",
                    "UPHENO:0063569",
                    "UPHENO:0004621",
                    "UPHENO:0002536",
                    "UPHENO:0008668",
                    "UPHENO:0080126",
                    "UPHENO:0081581",
                    "UPHENO:0005602",
                    "UBERON:0006058",
                    "HP:0002813",
                    "UBERON:0004923",
                    "UPHENO:0002983",
                    "HP:0002246",
                    "UBERON:0001007",
                    "UBERON:0002544",
                    "GO:0050789",
                    "UPHENO:0002949",
                    "UPHENO:0000543",
                    "UPHENO:0003004",
                    "UBERON:0002114",
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                    "UPHENO:0026757",
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                ],
                "has_phenotype_closure_label": [
                    "Abnormal skull morphology",
                    "Abnormality of skull size",
                    "Aplasia/Hypoplasia involving the central nervous system",
                    "axial skeleton plus cranial skeleton",
                    "postcranial axial skeletal system",
                    "skull",
                    "axial skeletal system",
                    "Microcephaly",
                    "Aplasia/Hypoplasia of the cerebrum",
                    "Abnormality of the genitourinary system",
                    "renal system",
                    "Abnormality of the upper urinary tract",
                    "excretory system",
                    "upper urinary tract phenotype",
                    "upper urinary tract",
                    "craniocervical region morphology phenotype",
                    "Abnormality of the head",
                    "Midface retrusion",
                    "anatomical entity hypoplasia in face",
                    "midface morphology phenotype",
                    "head morphology phenotype",
                    "Abnormality of the face",
                    "midface",
                    "cell",
                    "Abnormal bone marrow cell morphology",
                    "myeloid cell",
                    "skull morphology phenotype",
                    "hematopoietic cell",
                    "eukaryotic cell",
                    "cerebellum phenotype",
                    "segmental subdivision of hindbrain phenotype",
                    "hindbrain phenotype",
                    "cerebellum",
                    "posterior neural tube phenotype",
                    "organ subunit",
                    "formed cerebellum",
                    "Cerebellar malformation",
                    "segmental subdivision of nervous system phenotype",
                    "segmental subdivision of nervous system",
                    "formed multicellular anatomical structure",
                    "metencephalon morphology phenotype",
                    "metencephalon",
                    "Abnormal cerebellum morphology",
                    "chordal neural plate phenotype",
                    "Abnormal hindbrain morphology",
                    "chordal neural plate",
                    "central nervous system cell part cluster degeneration",
                    "kidney",
                    "cerebral hemisphere",
                    "brain white matter morphology phenotype",
                    "formed multi-tissue structure",
                    "ectoderm-derived structure degeneration",
                    "Abnormal periventricular white matter morphology",
                    "white matter degeneration",
                    "material anatomical entity degeneration",
                    "brain white matter phenotype",
                    "anatomical entity degeneration in central nervous system",
                    "central nervous system cell part cluster",
                    "white matter of telencephalon degeneration",
                    "Abnormal cerebral morphology",
                    "central nervous system cell part cluster phenotype",
                    "brain white matter",
                    "multi cell part structure",
                    "anatomical entity degeneration",
                    "white matter of forebrain degeneration",
                    "white matter phenotype",
                    "telencephalon phenotype",
                    "multi cell part structure degeneration",
                    "root",
                    "secretion by cell phenotype",
                    "reproductive structure phenotype",
                    "gastrula morphology phenotype",
                    "formed regional part of nervous system",
                    "signal release phenotype",
                    "reproductive organ phenotype",
                    "gland of diencephalon",
                    "biological regulation phenotype",
                    "epithelium",
                    "Abnormal megakaryocyte morphology",
                    "material anatomical entity physiology phenotype",
                    "multi-tissue structure phenotype",
                    "decreased regulation of hormone levels",
                    "reproductive gland morphology phenotype",
                    "cerebral hemisphere white matter morphology phenotype",
                    "neural plate",
                    "decreased cellular process",
                    "head phenotype",
                    "decreased biological regulation",
                    "growth hormone secretion",
                    "diencephalon",
                    "endocrine system morphology phenotype",
                    "reproductive gland phenotype",
                    "cellular process",
                    "Abnormal renal morphology",
                    "decreased signal release",
                    "cellular process phenotype",
                    "decreased qualitatively regulation of hormone levels",
                    "decreased peptide transport",
                    "reproductive system morphology phenotype",
                    "regional part of nervous system",
                    "decreased secretion by cell",
                    "export from cell phenotype",
                    "Abnormal forebrain morphology",
                    "cerebral hemisphere white matter degeneration",
                    "decreased peptide hormone secretion",
                    "compound organ phenotype",
                    "craniocervical region phenotype",
                    "establishment of localization phenotype",
                    "regional part of brain",
                    "telencephalon",
                    "Hypopituitarism",
                    "forebrain morphology phenotype",
                    "endocrine gland morphology phenotype",
                    "decreased qualitatively peptide transport",
                    "secretion",
                    "nitrogen compound transport",
                    "craniocervical region",
                    "glandular system",
                    "decreased establishment of localization",
                    "decreased qualitatively nitrogen compound transport",
                    "epithelium phenotype",
                    "cell-cell signaling",
                    "Eukaryota",
                    "nitrogen compound transport phenotype",
                    "decreased transport",
                    "Abnormality of the endocrine system",
                    "reproductive structure",
                    "decreased peptide secretion",
                    "decreased secretion in pituitary gland",
                    "segmental subdivision of hindbrain",
                    "biological_process in nervous system phenotype",
                    "decreased biological_process in brain",
                    "decreased qualitatively transport",
                    "decreased qualitatively amide transport",
                    "pituitary gland morphology phenotype",
                    "epithelial tube",
                    "biological regulation",
                    "transport phenotype",
                    "regional part of brain phenotype",
                    "gland morphology phenotype",
                    "decreased amide transport",
                    "growth hormone secretion phenotype",
                    "Abnormal metencephalon morphology",
                    "peptide transport",
                    "head",
                    "establishment of localization",
                    "decreased growth hormone secretion",
                    "export from cell",
                    "multi-tissue structure",
                    "Eumetazoa",
                    "Anterior hypopituitarism",
                    "decreased qualitatively cellular process",
                    "decreased hormone secretion",
                    "biological_process rate in brain phenotype",
                    "gland of diencephalon phenotype",
                    "decreased qualitatively secretion",
                    "neural tube phenotype",
                    "reproductive system phenotype",
                    "pre-chordal neural plate",
                    "decreased qualitatively localization",
                    "reproductive system",
                    "cellular organisms",
                    "forebrain phenotype",
                    "localization phenotype",
                    "peptide secretion phenotype",
                    "neural plate morphology phenotype",
                    "peptide secretion",
                    "hormone secretion",
                    "gland",
                    "anterior neural tube",
                    "anterior neural tube phenotype",
                    "endocrine gland phenotype",
                    "adenohypophysis",
                    "gland phenotype",
                    "diencephalon phenotype",
                    "face phenotype",
                    "regional part of nervous system phenotype",
                    "peptide transport phenotype",
                    "abdominal segment of trunk",
                    "trunk",
                    "number of anatomical enitites of type hemopoietic organ phenotype",
                    "increased number of abdominal viscera",
                    "increased number of anatomical structure in the abdomen",
                    "increased number of viscus",
                    "Abnormality of the cardiovascular system",
                    "viscus",
                    "abdominal segment element",
                    "Abnormality of the immune system",
                    "face",
                    "increased number of material anatomical entity",
                    "vascular system",
                    "Abnormality of the vasculature",
                    "decreased qualitatively biological_process in central nervous system",
                    "trunk phenotype",
                    "lymphatic part of lymphoid system phenotype",
                    "number of anatomical enitites of type viscus phenotype",
                    "spleen morphology phenotype",
                    "number of anatomical enitites of type abdomen element phenotype",
                    "increased number of organ",
                    "increased number of anatomical entity",
                    "lymphatic part of lymphoid system",
                    "Megakaryocyte dysplasia",
                    "cardiovascular system",
                    "disconnected anatomical group",
                    "increased number of anatomical structure",
                    "trunk region element phenotype",
                    "increased number of immune organ",
                    "subdivision of trunk phenotype",
                    "increased number of abdominal segment element",
                    "hemopoietic organ phenotype",
                    "amide transport phenotype",
                    "vasculature phenotype",
                    "mesoderm phenotype",
                    "subdivision of head",
                    "All",
                    "radius bone morphology phenotype",
                    "limb",
                    "diencephalon morphology phenotype",
                    "radius endochondral element",
                    "forelimb long bone",
                    "non-connected functional system",
                    "intestine phenotype",
                    "ecto-epithelium",
                    "Neoplasm by anatomical site",
                    "musculoskeletal system",
                    "genitourinary system",
                    "white matter of forebrain phenotype",
                    "limb long bone phenotype",
                    "white matter",
                    "decreased length of forelimb bone",
                    "closing of the subdivision of tube",
                    "number of anatomical enitites of type abdominal segment element phenotype",
                    "embryonic tissue phenotype",
                    "zeugopod",
                    "anatomical system phenotype",
                    "multicellular organism development phenotype",
                    "bone of free limb or fin",
                    "bone of pectoral complex",
                    "skeleton phenotype",
                    "musculature of body phenotype",
                    "material anatomical entity atresia",
                    "paired limb/fin segment",
                    "digit 1 phenotype",
                    "neural tube morphology phenotype",
                    "bone of pectoral complex morphology phenotype",
                    "decreased size of the anatomical structure in the pectoral complex",
                    "decreased length of organ",
                    "digestive system",
                    "pectoral complex",
                    "decreased length of bone element",
                    "anatomical collection",
                    "telencephalon morphology phenotype",
                    "secretion by cell",
                    "cardiovascular system phenotype",
                    "upper limb segment phenotype",
                    "Forearm undergrowth",
                    "Decreased head circumference",
                    "tissue phenotype",
                    "hindbrain morphology phenotype",
                    "radius bone hypoplasia",
                    "forelimb bone phenotype",
                    "lateral plate mesoderm phenotype",
                    "decreased size of the organ",
                    "autopod region morphology phenotype",
                    "appendage",
                    "neurectoderm phenotype",
                    "anatomical entity morphology in the pectoral complex phenotype",
                    "hematopoietic system phenotype",
                    "decreased nitrogen compound transport",
                    "long bone phenotype",
                    "mesenchyme morphology phenotype",
                    "forelimb morphology phenotype",
                    "anatomical structure phenotype",
                    "anatomical entity physiology phenotype",
                    "decreased length of anatomical structure",
                    "Abnormal digestive system morphology",
                    "Abnormal appendicular skeleton morphology",
                    "endochondral bone",
                    "epithelial tube phenotype",
                    "duodenum atresia",
                    "Abnormality of limb bone",
                    "limb segment",
                    "subdivision of skeleton phenotype",
                    "Supernumerary spleens",
                    "zeugopodial skeleton",
                    "germ layer / neural crest phenotype",
                    "Aplasia/Hypoplasia of the radius",
                    "long bone",
                    "cerebral hemisphere white matter phenotype",
                    "alimentary part of gastrointestinal system phenotype",
                    "skeleton of limb phenotype",
                    "forelimb bud phenotype",
                    "decreased size of the forelimb zeugopod bone",
                    "musculoskeletal system phenotype",
                    "aplasia or hypoplasia of anatomical entity",
                    "organ system subdivision",
                    "forelimb zeugopod phenotype",
                    "limb endochondral element phenotype",
                    "Abnormality of the hypothalamus-pituitary axis",
                    "Upper limb undergrowth",
                    "decreased qualitatively establishment of localization",
                    "Abnormal duodenum morphology",
                    "decreased qualitatively export from cell",
                    "decreased length of endochondral bone",
                    "Decreased response to growth hormone stimulation test",
                    "decreased size of the endochondral element",
                    "brain ventricle/choroid plexus",
                    "limb endochondral element",
                    "paired limb/fin bud",
                    "limb bone morphology phenotype",
                    "absent anatomical structure in the forelimb",
                    "forelimb endochondral element",
                    "decreased length of skeletal element",
                    "multicellular organism",
                    "decreased size of the forelimb bone",
                    "increased number of anatomical entity in the abdomen",
                    "nervous system morphology phenotype",
                    "decreased size of the long bone",
                    "autopodial extension phenotype",
                    "Abnormality of the spleen",
                    "forelimb skeleton phenotype",
                    "decreased qualitatively anatomical structure development",
                    "Abnormal skeletal morphology",
                    "absent material anatomical entity in the limb bud",
                    "radius bone phenotype",
                    "decreased length of multicellular anatomical structure",
                    "surface structure",
                    "decreased size of the skeletal element",
                    "anatomical structure development phenotype",
                    "increased number of multicellular anatomical structure",
                    "endochondral bone phenotype",
                    "digit morphology phenotype",
                    "limb bud phenotype",
                    "decreased localization",
                    "arm",
                    "subdivision of tube atresia",
                    "Phenotypic abnormality",
                    "limb skeleton subdivision",
                    "hematopoietic system",
                    "abdomen element phenotype",
                    "limb segment phenotype",
                    "endochondral element phenotype",
                    "anatomical entity atresia",
                    "pectoral appendage",
                    "pituitary gland",
                    "material anatomical entity",
                    "circulatory system",
                    "autopod region",
                    "development of anatomical entity phenotype",
                    "Myelodysplasia",
                    "organ",
                    "Abnormal upper limb bone morphology",
                    "bone of pectoral complex phenotype",
                    "Leukoencephalopathy",
                    "immune system",
                    "forelimb bud morphology phenotype",
                    "musculature phenotype",
                    "developing anatomical structure phenotype",
                    "subdivision of digestive tract",
                    "regulation of hormone levels",
                    "independent continuant",
                    "kidney hypoplasia",
                    "decreased secretion",
                    "decreased length of arm bone",
                    "digestive system morphology phenotype",
                    "number of anatomical enitites of type immune organ phenotype",
                    "Intestinal atresia",
                    "digestive system element phenotype",
                    "material anatomical entity phenotype",
                    "Abnormality of the kidney",
                    "hypothalamus-pituitary axis",
                    "Gastrointestinal atresia",
                    "bone marrow",
                    "Abnormality of the digestive system",
                    "signal release",
                    "Abnormal forearm morphology",
                    "limb bone phenotype",
                    "system",
                    "appendage phenotype",
                    "skeletal element phenotype",
                    "presumptive structure phenotype",
                    "skeleton",
                    "pectoral appendage bud phenotype",
                    "small intestine",
                    "intestine morphology phenotype",
                    "increased size of the ectoderm-derived structure",
                    "germ layer phenotype",
                    "embryonic structure phenotype",
                    "white matter of telencephalon",
                    "absent multicellular anatomical structure in the limb",
                    "organism subdivision",
                    "absent multicellular anatomical structure",
                    "anatomical conduit",
                    "developing anatomical structure",
                    "digestive system element",
                    "hormone transport",
                    "Opisthokonta",
                    "embryo morphology phenotype",
                    "aplasia or hypoplasia of radius bone",
                    "forelimb zeugopod",
                    "skull phenotype",
                    "alimentary part of gastrointestinal system morphology phenotype",
                    "Aplasia/hypoplasia involving bones of the upper limbs",
                    "appendicular skeleton phenotype",
                    "small intestine phenotype",
                    "central nervous system",
                    "closing of the anatomical entity",
                    "amide transport",
                    "multicellular anatomical structure phenotype",
                    "increased number of material anatomical entity in the abdomen",
                    "organ part",
                    "size of anatomical entity phenotype",
                    "small intestine morphology phenotype",
                    "Metazoa",
                    "absent manual digit",
                    "decreased size of the anatomical entity",
                    "lateral structure phenotype",
                    "Abnormality of head or neck",
                    "formed regional part of brain",
                    "anatomical structure atresia",
                    "decreased length of limb endochondral element",
                    "limb bone",
                    "closing of the anatomical system",
                    "neural tube",
                    "acropodium region",
                    "anatomical system",
                    "forelimb zeugopod bone hypoplasia",
                    "intestine",
                    "skeletal system morphology phenotype",
                    "process",
                    "multicellular anatomical structure",
                    "Abnormality of the nervous system",
                    "closing of the multicellular anatomical structure",
                    "forelimb bone",
                    "secretion phenotype",
                    "regulation of biological process",
                    "Abnormality of the skeletal system",
                    "Abnormal gastrointestinal tract morphology",
                    "bone of free limb or fin phenotype",
                    "paired limb/fin skeleton phenotype",
                    "decreased length of long bone",
                    "increased number of hemopoietic organ",
                    "anatomical entity morphology phenotype",
                    "decreased size of the multicellular anatomical structure in the pectoral complex",
                    "closing of the subdivision of digestive tract",
                    "decreased anatomical structure development",
                    "decreased size of the bone of pectoral complex",
                    "surface structure phenotype",
                    "anatomical entity morphology in the manus phenotype",
                    "abdomen",
                    "embryo phenotype",
                    "cavitated compound organ phenotype",
                    "malformed anatomical entity",
                    "Abnormal cerebral white matter morphology",
                    "anatomical structure",
                    "alimentary part of gastrointestinal system atresia",
                    "anatomical entity",
                    "embryonic structure",
                    "limb phenotype",
                    "midface phenotype",
                    "multicellular anatomical structure atresia",
                    "embryonic autopod plate morphology phenotype",
                    "postcranial axial skeleton",
                    "closing of the material anatomical entity",
                    "paired limb/fin bud phenotype",
                    "mesoderm-derived structure phenotype",
                    "decreased length of endochondral element",
                    "decreased size of the arm bone",
                    "closing of the organ part",
                    "entity",
                    "growth",
                    "cavitated compound organ",
                    "manual digit phenotype",
                    "closing of the anatomical structure",
                    "material entity",
                    "duodenum",
                    "brain ventricle morphology phenotype",
                    "forelimb endochondral element phenotype",
                    "Duodenal atresia",
                    "Aplasia/hypoplasia involving the skeleton",
                    "Abnormality of the upper limb",
                    "Abnormal endocrine physiology",
                    "Abnormal small intestine morphology",
                    "embryo",
                    "subdivision of skeletal system phenotype",
                    "appendage girdle complex",
                    "decreased size of the bone of appendage girdle complex",
                    "radius bone",
                    "forelimb bud",
                    "Abnormal cerebral subcortex morphology",
                    "cell communication",
                    "blood island",
                    "Abnormal long bone morphology",
                    "Abnormality of the hand",
                    "bone of appendage girdle complex phenotype",
                    "tube phenotype",
                    "germ layer",
                    "embryo development",
                    "continuant",
                    "phenotype",
                    "megakaryocyte",
                    "decreased biological_process",
                    "genitourinary system phenotype",
                    "presumptive structure",
                    "anatomical system atresia",
                    "anatomical entity phenotype",
                    "anatomical conduit phenotype",
                    "Abnormality of limbs",
                    "duodenum morphology phenotype",
                    "multicellular organism phenotype",
                    "limb bud",
                    "Growth abnormality",
                    "metencephalon phenotype",
                    "mesoderm-derived structure",
                    "forelimb skeleton",
                    "paired limb/fin phenotype",
                    "manus morphology phenotype",
                    "Abnormality of the musculoskeletal system",
                    "digit 1",
                    "delayed growth",
                    "intestine atresia",
                    "blood island phenotype",
                    "subdivision of digestive tract atresia",
                    "Abnormal forearm bone morphology",
                    "forelimb",
                    "Abnormality of the urinary system",
                    "developmental process",
                    "decreased length of limb bone",
                    "regulation of hormone levels phenotype",
                    "upper limb segment",
                    "manual digit 1 plus metapodial segment",
                    "regulation of biological quality",
                    "aplasia or hypoplasia of skeleton",
                    "mesoderm morphology phenotype",
                    "decreased size of the multicellular anatomical structure",
                    "cerebral hemisphere morphology phenotype",
                    "paired limb/fin segment phenotype",
                    "kidney phenotype",
                    "Abnormality of the abdominal organs",
                    "limb long bone",
                    "long bone morphology phenotype",
                    "decreased length of forelimb endochondral element",
                    "anatomical entity hypoplasia",
                    "peptide hormone secretion",
                    "biological_process rate phenotype",
                    "anatomical entity morphology in the appendage girdle complex phenotype",
                    "absent autopodial extension",
                    "lateral plate mesoderm",
                    "Abnormal midface morphology",
                    "paired limb/fin",
                    "brain ventricle/choroid plexus phenotype",
                    "skeletal element",
                    "subdivision of organism along appendicular axis",
                    "forelimb zeugopod bone",
                    "bone element",
                    "germ layer / neural crest",
                    "brain ventricle phenotype",
                    "Short long bone",
                    "forelimb zeugopod skeleton",
                    "decreased length of material anatomical entity",
                    "taxon specific phenotype",
                    "number of anatomical enitites of type organ phenotype",
                    "decreased size of the material anatomical entity in the pectoral complex",
                    "Growth delay",
                    "limb long bone morphology phenotype",
                    "Aplasia/hypoplasia involving forearm bones",
                    "reproductive gland",
                    "alimentary part of gastrointestinal system",
                    "subdivision of skeletal system",
                    "subdivision of tube phenotype",
                    "musculature",
                    "skeletal system",
                    "Abnormal axial skeleton morphology",
                    "decreased qualitatively biological regulation",
                    "subdivision of skeleton",
                    "increased number of mesoderm-derived structure",
                    "skeleton of pectoral complex",
                    "cranial skeletal system",
                    "decreased size of the limb bone",
                    "appendicular skeleton",
                    "Polysplenia",
                    "Abnormal morphology of the radius",
                    "embryo development phenotype",
                    "zeugopod phenotype",
                    "immune organ phenotype",
                    "forelimb phenotype",
                    "absent digit",
                    "decreased size of the endochondral bone",
                    "anatomical entity morphology in the alimentary part of gastrointestinal system phenotype",
                    "decreased size of the mesoderm-derived structure",
                    "decreased biological_process in pituitary gland",
                    "anatomical entity length phenotype",
                    "organ subunit phenotype",
                    "anatomical cluster phenotype",
                    "anatomical entity morphology in the skeleton of pectoral complex phenotype",
                    "ectoderm-derived structure phenotype",
                    "decreased biological_process in multicellular organism",
                    "paired limb/fin skeleton",
                    "Aplasia/Hypoplasia of fingers",
                    "mesoderm",
                    "appendicular skeleton morphology phenotype",
                    "subdivision of organism along main body axis",
                    "germ layer morphology phenotype",
                    "decreased length of bone of pectoral complex",
                    "subdivision of head phenotype",
                    "anterior region of body",
                    "Aplasia/hypoplasia involving bones of the extremities",
                    "renal system morphology phenotype",
                    "forelimb long bone phenotype",
                    "manus phenotype",
                    "mesenchyme phenotype",
                    "compound organ",
                    "megakaryocyte morphology phenotype",
                    "ventricular system of brain",
                    "dense mesenchyme tissue phenotype",
                    "Abnormal response to endocrine stimulation test",
                    "presumptive ectoderm",
                    "localization",
                    "forelimb zeugopod bone phenotype",
                    "anatomical collection phenotype",
                    "organism subdivision phenotype",
                    "embryonic tissue",
                    "digestive tract",
                    "mesenchyme",
                    "endocrine gland",
                    "brain",
                    "reproductive organ",
                    "pectoral appendage skeleton phenotype",
                    "Aplasia/hypoplasia of the extremities",
                    "embryonic tissue morphology phenotype",
                    "Renal hypoplasia/aplasia",
                    "decreased export from cell",
                    "forelimb zeugopod bone morphology phenotype",
                    "anatomical structure degeneration",
                    "lymphoid system phenotype",
                    "multi-limb segment region",
                    "appendicular skeletal system",
                    "viscus phenotype",
                    "formed anatomical structure",
                    "limb bud morphology phenotype",
                    "white matter of telencephalon phenotype",
                    "arm bone phenotype",
                    "subdivision of tube",
                    "ventricular system of central nervous system",
                    "brain white matter degeneration",
                    "decreased size of the bone element",
                    "bone marrow cell",
                    "cerebellum morphology phenotype",
                    "lateral structure",
                    "structure with developmental contribution from neural crest",
                    "increased size of the anatomical structure",
                    "decreased size of the forelimb endochondral element",
                    "central nervous system morphology phenotype",
                    "skeleton of limb",
                    "dense mesenchyme tissue",
                    "endocrine system",
                    "hemolymphoid system",
                    "number of anatomical enitites of type anatomical structure phenotype",
                    "increased number of trunk region element",
                    "spleen",
                    "Neoplasm",
                    "neoplasm phenotype",
                    "spleen phenotype",
                    "digestive system phenotype",
                    "multicellular organism morphology phenotype",
                    "Hematological neoplasm",
                    "signaling",
                    "delayed biological_process",
                    "limb morphology phenotype",
                    "occurrent",
                    "aplasia or hypoplasia of telencephalon",
                    "manual digit plus metapodial segment",
                    "multi-limb segment region phenotype",
                    "biological_process",
                    "renal/urinary system phenotype",
                    "biological_process phenotype",
                    "ectoderm-derived structure",
                    "Abnormal intestine morphology",
                    "anatomical structure development",
                    "gastrula",
                    "multicellular organismal process phenotype",
                    "decreased developmental process",
                    "adenohypophysis phenotype",
                    "endocrine system physiology phenotype",
                    "endochondral element",
                    "decreased qualitatively biological_process",
                    "absent organism subdivision in the multicellular organism",
                    "forebrain",
                    "absent anatomical entity in the forelimb",
                    "decreased embryo development",
                    "decreased multicellular organismal process",
                    "developmental process phenotype",
                    "digit",
                    "decreased qualitatively developmental process",
                    "neural plate phenotype",
                    "decreased qualitatively multicellular organismal process",
                    "phenotypic effect",
                    "embryo development rate phenotype",
                    "arm phenotype",
                    "decreased qualitatively embryo development",
                    "number of anatomical enitites of type material anatomical entity phenotype",
                    "hindbrain",
                    "Abnormality of the anterior pituitary",
                    "multicellular organismal process",
                    "digit plus metapodial segment",
                    "decreased multicellular organism development",
                    "manual digitopodium region",
                    "size of skull phenotype",
                    "growth phenotype",
                    "developmental process rate phenotype",
                    "renal system phenotype",
                    "manus",
                    "ectoderm morphology phenotype",
                    "multicellular organism development",
                    "Intrauterine growth retardation",
                    "increased size of the organ part",
                    "decreased qualitatively secretion by cell",
                    "anatomical wall phenotype",
                    "endocrine system phenotype",
                    "Abnormal cerebral ventricle morphology",
                    "anatomical entity morphology in the brain phenotype",
                    "Abnormal nervous system morphology",
                    "subdivision of digestive tract phenotype",
                    "nervous system",
                    "Morphological central nervous system abnormality",
                    "structure with developmental contribution from neural crest phenotype",
                    "size of brain ventricle phenotype",
                    "increased size of the brain ventricle",
                    "midface hypoplasia",
                    "brain ventricle/choroid plexus morphology phenotype",
                    "formed material anatomical entity",
                    "brain phenotype",
                    "ventricle of nervous system phenotype",
                    "future nervous system",
                    "presumptive ectoderm phenotype",
                    "bone of appendage girdle complex",
                    "increased size of the ventricle of nervous system",
                    "Abnormality of the gastrointestinal tract",
                    "Abnormal brain morphology",
                    "increased number of spleen",
                    "increased size of the brain ventricle/choroid plexus",
                    "organ component layer phenotype",
                    "future central nervous system",
                    "ventricle of nervous system",
                    "lateral plate mesoderm morphology phenotype",
                    "organ system subdivision phenotype",
                    "increased size of the anatomical entity",
                    "absent anatomical structure",
                    "pituitary gland phenotype",
                    "pectoral appendage bud",
                    "central nervous system phenotype",
                    "limb skeleton subdivision phenotype",
                    "brain ventricle",
                    "increased size of the organ component layer",
                    "organ component layer",
                    "anatomical wall",
                    "brain morphology phenotype",
                    "absent anatomical structure in the multicellular organism",
                    "multi cell part structure phenotype",
                    "increased size of the multicellular anatomical structure",
                    "Abnormal limb bone morphology",
                    "neurectoderm",
                    "aplastic manual digit 1",
                    "transport",
                    "Hypoplasia of the radius",
                    "future central nervous system phenotype",
                    "ectoderm",
                    "increased size of the material anatomical entity",
                    "vasculature",
                    "Abnormal spleen morphology",
                    "nervous system phenotype",
                    "skeletal system phenotype",
                    "blastula",
                    "Limb undergrowth",
                    "musculature of body",
                    "number of anatomical enitites of type organism subdivision phenotype",
                    "cerebral hemisphere white matter",
                    "decreased size of the anatomical entity in the pectoral complex",
                    "Ventriculomegaly",
                    "digit 1 or 5 phenotype",
                    "kidney morphology phenotype",
                    "immune system phenotype",
                    "decreased qualitatively hormone transport",
                    "decreased size of the limb endochondral element",
                    "digit 1 plus metapodial segment",
                    "pectoral appendage phenotype",
                    "Abnormal finger morphology",
                    "Absent thumb",
                    "circulatory system phenotype",
                    "organ part phenotype",
                    "absent anatomical structure in the limb",
                    "bone element phenotype",
                    "digit phenotype",
                    "Renal hypoplasia",
                    "posterior neural tube",
                    "hemopoietic organ morphology phenotype",
                    "Abnormality of blood and blood-forming tissues",
                    "Aplasia/Hypoplasia of the thumb",
                    "absent material anatomical entity in the limb",
                    "number of anatomical enitites of type multicellular anatomical structure phenotype",
                    "segment of autopod",
                    "absent multicellular anatomical structure in the multicellular organism",
                    "absent anatomical entity in the multicellular organism",
                    "absent anatomical entity in the limb bud",
                    "biological_process in central nervous system phenotype",
                    "absent material anatomical entity in the multicellular organism",
                    "digit 1 or 5",
                    "Abnormal radial ray morphology",
                    "increased number of multicellular anatomical structure in the abdomen",
                    "autopodial skeleton",
                    "craniofacial/craniocervical phenotype",
                    "white matter of forebrain",
                    "cerebral subcortex",
                    "agenesis of anatomical entity",
                    "Finger aplasia",
                    "decreased hormone transport",
                    "absent anatomical entity",
                    "face morphology phenotype",
                    "ecto-epithelium phenotype",
                    "autopodial extension",
                    "forelimb zeugopod morphology phenotype",
                    "Abnormal thumb morphology",
                    "abdominal viscera phenotype",
                    "absent multicellular anatomical structure in the forelimb",
                    "manual digit morphology in the manus phenotype",
                    "Abnormal digit morphology",
                    "embryonic autopod plate",
                    "Abnormal hand morphology",
                    "subdivision of organism along appendicular axis phenotype",
                    "organ phenotype",
                    "manual digit 1 or 5",
                    "absent material anatomical entity in the forelimb",
                    "absent organism subdivision",
                    "decreased size of the anatomical structure",
                    "manual digit",
                    "skeleton of manus",
                    "absent anatomical entity in the limb",
                    "formed ectoderm-derived structure",
                    "number of anatomical enitites of type anatomical entity phenotype",
                    "tissue",
                    "decreased length of mesoderm-derived structure",
                    "decreased length of bone of appendage girdle complex",
                    "absent material anatomical entity",
                    "bone cell",
                    "manual digit 1",
                    "segment of manus",
                    "ectoderm phenotype",
                    "subdivision of trunk",
                    "cranial skeletal system phenotype",
                    "tube",
                    "digitopodium region",
                    "cell phenotype",
                    "Abnormality of the lymphatic system",
                    "decreased size of the bone of free limb or fin",
                    "autopod region phenotype",
                    "decreased qualitatively hormone secretion",
                    "aplasia or hypoplasia of manual digit 1",
                    "manual digit 1 morphology phenotype",
                    "decreased length of bone of free limb or fin",
                    "decreased size of the material anatomical entity",
                    "Aplasia/hypoplasia involving bones of the hand",
                    "pectoral appendage skeleton",
                    "aplastic anatomical entity",
                    "abdominal segment element phenotype",
                    "subdivision of organism along main body axis phenotype",
                    "Abnormal pituitary gland morphology",
                    "arm bone",
                    "hemopoietic organ",
                    "decreased qualitatively multicellular organism development",
                    "immune organ",
                    "trunk region element",
                    "anatomical cluster",
                    "Chiari malformation",
                    "aplasia or hypoplasia of manual digit",
                    "lymphoid system",
                    "abdomen element",
                    "decreased length of forelimb zeugopod bone",
                    "abdominal viscera",
                    "immune system morphology phenotype",
                    "main body axis",
                    "organ part atresia",
                    "body proper",
                    "pre-chordal neural plate phenotype",
                    "number of anatomical enitites of type trunk region element phenotype",
                    "hypothalamus-pituitary axis phenotype",
                    "duodenum phenotype",
                    "increased number of abdomen element",
                    "decreased length of anatomical entity",
                    "number of anatomical enitites of type mesoderm-derived structure phenotype",
                    "decreased qualitatively signal release",
                    "hematopoietic system morphology phenotype",
                ],
                "has_phenotype_count": 16,
                "score": None,
                "exact_synonyms": ["Fanconi anemia, complementation group W"],
                "related_synonyms": ["FANCW"],
                "highlighting": None,
            },
            {
                "id": "MONDO:1011448",
                "category": "biolink:Disease",
                "name": "Fanconi syndrome, non-human animal",
                "full_name": None,
                "deprecated": None,
                "description": "Fanconi syndrome that occurs in non-human animals.",
                "xref": ["OMIA:000366"],
                "provided_by": "phenio_nodes",
                "in_taxon": None,
                "in_taxon_label": None,
                "symbol": None,
                "synonym": None,
                "broad_synonym": None,
                "exact_synonym": None,
                "narrow_synonym": None,
                "related_synonym": None,
                "subsets": None,
                "uri": None,
                "iri": None,
                "namespace": "MONDO",
                "has_phenotype": None,
                "has_phenotype_label": None,
                "has_phenotype_closure": None,
                "has_phenotype_closure_label": None,
                "has_phenotype_count": 0,
                "score": None,
                "highlighting": None,
            },
            {
                "id": "MONDO:0012186",
                "category": "biolink:Disease",
                "name": "Fanconi anemia complementation group I",
                "full_name": None,
                "deprecated": None,
                "description": "Fanconi anemia caused by mutations in the FANCI gene, encoding Fanconi anemia group I protein.",
                "xref": [
                    "DOID:0111091",
                    "GARD:15448",
                    "MEDGEN:323016",
                    "MESH:C563802",
                    "NCIT:C129026",
                    "OMIM:609053",
                    "UMLS:C1836861",
                ],
                "provided_by": "phenio_nodes",
                "in_taxon": None,
                "in_taxon_label": None,
                "symbol": None,
                "synonym": [
                    "FANCI",
                    "Fanconi Anemia, complementation Group 1",
                    "Fanconi Anemia, complementation group type 1",
                    "Fanconi anaemia complementation group type I",
                    "Fanconi anemia complementation group I",
                    "Fanconi anemia complementation group type I",
                    "Fanconi anemia, complementation group I",
                ],
                "broad_synonym": None,
                "exact_synonym": None,
                "narrow_synonym": None,
                "related_synonym": None,
                "subsets": ["clingen", "gard_rare", "nord_rare", "otar", "rare"],
                "uri": None,
                "iri": None,
                "namespace": "MONDO",
                "has_phenotype": [
                    "HP:0001655",
                    "HP:0001875",
                    "HP:0000325",
                    "HP:0000545",
                    "HP:0002984",
                    "HP:0002247",
                    "HP:0003974",
                    "HP:0001873",
                    "HP:0009778",
                    "HP:0001631",
                    "HP:0000543",
                    "HP:0001511",
                    "HP:0000405",
                    "HP:0009777",
                    "HP:0000568",
                    "HP:0000821",
                    "HP:0002308",
                    "HP:0002949",
                    "HP:0000609",
                    "HP:0034323",
                    "HP:0000470",
                    "HP:0001263",
                    "HP:0003221",
                    "HP:0030048",
                    "HP:0000076",
                    "HP:0000252",
                    "HP:0000413",
                    "HP:0001643",
                    "HP:0005528",
                    "HP:0000957",
                    "HP:0001903",
                    "HP:0001629",
                    "HP:0010034",
                    "HP:0012506",
                    "HP:0000085",
                    "HP:0001274",
                    "HP:0004322",
                    "HP:0000089",
                    "HP:0000365",
                    "HP:0000483",
                    "HP:0004325",
                    "HP:0001331",
                    "HP:0030680",
                    "HP:0012210",
                    "HP:0005528",
                ],
                "has_phenotype_label": [
                    "Patent foramen ovale",
                    "Decreased total neutrophil count",
                    "Triangular face",
                    "Myopia",
                    "Hypoplasia of the radius",
                    "Duodenal atresia",
                    "Absent radius",
                    "Thrombocytopenia",
                    "Short thumb",
                    "Atrial septal defect",
                    "Optic disc pallor",
                    "Intrauterine growth retardation",
                    "Conductive hearing impairment",
                    "Absent thumb",
                    "Microphthalmia",
                    "Hypothyroidism",
                    "Chiari malformation",
                    "Fused cervical vertebrae",
                    "Optic nerve hypoplasia",
                    "Reduced circulating growth hormone concentration",
                    "Short neck",
                    "Global developmental delay",
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                    "UPHENO:0052160",
                    "GO:0009059",
                    "UBERON:0001017",
                    "UPHENO:0005596",
                    "GO:0065008",
                    "UPHENO:0011567",
                    "UPHENO:0002638",
                    "GO:0048856",
                    "UBERON:0005856",
                    "UPHENO:0081436",
                    "UPHENO:0005647",
                    "HP:0000370",
                    "UPHENO:0076718",
                    "UPHENO:0052161",
                    "UPHENO:0052159",
                    "UPHENO:0087334",
                    "UPHENO:0002240",
                    "UPHENO:0005437",
                    "UPHENO:0011553",
                    "UBERON:0001690",
                    "UPHENO:0003459",
                    "UBERON:0011138",
                    "UPHENO:0009056",
                    "UPHENO:0052165",
                    "GO:0007605",
                    "HP:0000405",
                    "HP:0009115",
                    "UBERON:0000955",
                    "UBERON:0002105",
                    "UPHENO:0002668",
                    "UPHENO:0002433",
                    "UPHENO:0002950",
                    "UBERON:0003821",
                    "GO:0003008",
                    "UPHENO:0076901",
                    "UPHENO:0076730",
                    "UBERON:0001756",
                    "GO:0050954",
                    "UPHENO:0052231",
                    "UPHENO:0026108",
                    "UPHENO:0009382",
                    "UPHENO:0011825",
                    "UPHENO:0076744",
                    "HP:0009777",
                    "UPHENO:0009146",
                    "UBERON:0001009",
                    "HP:0002973",
                    "UPHENO:0068914",
                    "UPHENO:0027231",
                    "HP:0008056",
                    "UBERON:0002368",
                    "HP:0000925",
                    "UBERON:0002530",
                    "UPHENO:0066907",
                    "UPHENO:0066911",
                    "UPHENO:0066934",
                    "HP:0002242",
                    "UPHENO:0071310",
                    "UPHENO:0024906",
                    "UPHENO:0046467",
                    "UBERON:0000949",
                    "UPHENO:0063787",
                    "UPHENO:0066930",
                    "UPHENO:0074229",
                    "UPHENO:0002529",
                    "UPHENO:0009399",
                    "HP:0000821",
                    "UBERON:0011215",
                    "UPHENO:0076695",
                    "UPHENO:0002388",
                    "UPHENO:0002880",
                    "HP:0000818",
                    "UPHENO:0049829",
                    "UBERON:0015204",
                    "GO:0140352",
                    "UBERON:0010913",
                    "UPHENO:0002736",
                    "UPHENO:0071344",
                    "UBERON:0002616",
                    "HP:0000325",
                    "UBERON:0006598",
                    "UPHENO:0049647",
                    "UPHENO:0081554",
                    "UBERON:0004732",
                    "UBERON:0003057",
                    "UPHENO:0074584",
                    "GO:0009914",
                    "UBERON:0001049",
                    "HP:0002308",
                    "UPHENO:0031254",
                    "UPHENO:0084448",
                    "UPHENO:0075948",
                    "UPHENO:0071339",
                    "UPHENO:0086932",
                    "UPHENO:0025852",
                    "UPHENO:0076805",
                    "UPHENO:0081601",
                    "UBERON:0005177",
                    "UPHENO:0003066",
                    "UBERON:0001895",
                    "UPHENO:0002813",
                    "UBERON:0005358",
                    "UPHENO:0003017",
                    "UBERON:0006072",
                    "UBERON:0004733",
                    "UPHENO:0076723",
                    "UPHENO:0003237",
                    "UPHENO:0002934",
                    "UPHENO:0082875",
                    "UPHENO:0025883",
                    "UPHENO:0049966",
                    "UBERON:0002329",
                    "UBERON:0007530",
                    "UPHENO:0025544",
                    "HP:0001507",
                    "CHEBI:24431",
                    "UBERON:0005434",
                    "HP:0000356",
                    "UPHENO:0078068",
                    "HP:0003221",
                    "UPHENO:0078092",
                    "HP:0030680",
                    "UPHENO:0003234",
                    "UPHENO:0078122",
                    "UBERON:0000974",
                    "UPHENO:0008998",
                    "UBERON:0007285",
                    "UPHENO:0003191",
                    "UBERON:0011585",
                    "UPHENO:0078169",
                    "UBERON:0010409",
                    "UPHENO:0004484",
                    "HP:0011875",
                    "UPHENO:0078067",
                    "UBERON:0003077",
                    "UBERON:0012477",
                    "UPHENO:0011938",
                    "UBERON:0003458",
                    "HP:0000252",
                    "UBERON:0004086",
                    "UBERON:0008001",
                    "HP:0012759",
                    "UBERON:0002413",
                    "UBERON:0003056",
                    "UBERON:0003059",
                    "UPHENO:0002269",
                    "UPHENO:0010850",
                    "UPHENO:0002689",
                    "UPHENO:0066918",
                    "UPHENO:0002547",
                    "UPHENO:0074228",
                    "HP:0032251",
                    "UBERON:0006077",
                    "UPHENO:0002537",
                    "UPHENO:0050234",
                    "UBERON:0001130",
                    "UBERON:0002090",
                    "UBERON:0000982",
                    "UBERON:0012150",
                    "UBERON:0000948",
                    "UBERON:0005944",
                    "UPHENO:0002576",
                    "UPHENO:0078098",
                    "GO:0071705",
                    "UPHENO:0002693",
                    "UPHENO:0078089",
                    "UBERON:0015023",
                    "HP:0011843",
                    "UBERON:0004247",
                    "UBERON:0004451",
                    "UPHENO:0078139",
                    "UPHENO:0002654",
                    "HP:0009601",
                    "UPHENO:0087943",
                    "UPHENO:0002928",
                    "UBERON:0004905",
                    "UPHENO:0087563",
                    "UPHENO:0081440",
                    "UPHENO:0002301",
                    "UPHENO:0002543",
                    "UPHENO:0002616",
                    "UPHENO:0003074",
                    "UBERON:0011216",
                    "GO:0005623",
                    "UBERON:0001137",
                    "UBERON:0008962",
                    "UPHENO:0068838",
                    "UBERON:0005256",
                    "UBERON:0004288",
                    "UPHENO:0080208",
                    "HP:0000609",
                    "UBERON:0004770",
                    "HP:0002977",
                    "UPHENO:0086480",
                    "GO:0030072",
                    "UPHENO:0081264",
                    "UPHENO:0049890",
                    "UPHENO:0002869",
                    "HP:0032367",
                    "UPHENO:0002963",
                    "UPHENO:0049813",
                    "UPHENO:0050068",
                    "UPHENO:0050014",
                    "UPHENO:0086172",
                    "UBERON:0000179",
                    "GO:0051179",
                    "UPHENO:0002219",
                    "UPHENO:0026073",
                    "GO:0007154",
                    "UBERON:0001015",
                    "GO:0006810",
                    "GO:0030252",
                    "GO:0002790",
                    "UPHENO:0025955",
                    "UBERON:0000178",
                    "CL:0000764",
                    "UPHENO:0084763",
                    "UPHENO:0050065",
                    "UPHENO:0041465",
                    "HP:0025668",
                    "UPHENO:0049835",
                    "BFO:0000040",
                    "UPHENO:0003189",
                    "HP:0000470",
                    "HP:0003319",
                    "UBERON:0005401",
                    "HP:0012758",
                    "UPHENO:0026023",
                    "UPHENO:0049652",
                    "UPHENO:0025935",
                    "HP:0011100",
                    "UPHENO:0049837",
                    "HP:0025015",
                    "UPHENO:0004476",
                    "HP:0040012",
                ],
                "has_phenotype_closure_label": [
                    "absent material anatomical entity in the brain ventricle",
                    "lamina phenotype",
                    "absent cell layer",
                    "number of anatomical enitites of type lamina phenotype",
                    "septum pellucidum",
                    "gray matter of forebrain",
                    "immaterial anatomical entity",
                    "absent ectoderm-derived structure in the brain ventricle/choroid plexus",
                    "absent anatomical structure in the brain ventricle/choroid plexus",
                    "absent tissue",
                    "immaterial entity",
                    "absent multicellular anatomical structure in the brain ventricle",
                    "immaterial anatomical entity phenotype",
                    "cerebral hemisphere gray matter",
                    "Abnormal septum pellucidum morphology",
                    "absent material anatomical entity in the brain ventricle/choroid plexus",
                    "absent multicellular anatomical structure in the brain",
                    "anatomical space",
                    "absent multicellular anatomical structure in the brain ventricle/choroid plexus",
                    "cell layer phenotype",
                    "absent ectoderm-derived structure in the brain ventricle",
                    "anatomical space phenotype",
                    "brain gray matter phenotype",
                    "gray matter of telencephalon",
                    "brain gray matter",
                    "absent anatomical entity in the brain ventricle/choroid plexus",
                    "multicellular anatomical structure mass phenotype",
                    "Decreased multicellular organism mass",
                    "anatomical structure mass phenotype",
                    "anatomical entity mass phenotype",
                    "decreased anatomical structure mass",
                    "Astigmatism",
                    "curved anatomical entity",
                    "neural crest-derived structure, asymmetrically curved phenotype",
                    "anatomical structure, asymmetrically curved phenotype",
                    "structure with developmental contribution from neural crest, curved phenotype",
                    "material anatomical entity, asymmetrically curved phenotype",
                    "Abnormal anterior eye segment morphology",
                    "anterior segment of eyeball morphology phenotype",
                    "multicellular anatomical structure, curved phenotype",
                    "ocular surface region",
                    "anterior segment of eyeball",
                    "cornea phenotype",
                    "ectoderm-derived structure, asymmetrically curved phenotype",
                    "Abnormal cornea morphology",
                    "shape of cornea phenotype",
                    "cornea",
                    "material anatomical entity mass phenotype",
                    "tunica fibrosa of eyeball",
                    "kidney hypoplasia",
                    "Renal hypoplasia/aplasia",
                    "Renal hypoplasia",
                    "size of multicellular organism phenotype",
                    "Abnormality of body height",
                    "decreased material anatomical entity mass",
                    "decreased height of the multicellular organism",
                    "multicellular organism height phenotype",
                    "decreased height of the anatomical entity",
                    "absent axon tract",
                    "dorsal telencephalic commissure morphology phenotype",
                    "Agenesis of corpus callosum",
                    "brain commissure",
                    "cerebral hemisphere white matter phenotype",
                    "brain commissure morphology phenotype",
                    "white matter",
                    "number of anatomical enitites of type tract of brain phenotype",
                    "cerebral hemisphere",
                    "dorsal telencephalic commissure",
                    "absent intercerebral commissure",
                    "Abnormal corpus callosum morphology",
                    "number of anatomical enitites of type corpus callosum phenotype",
                    "number of anatomical enitites of type axon tract phenotype",
                    "brain white matter morphology phenotype",
                    "commissure of telencephalon phenotype",
                    "absent tract of brain",
                    "number of anatomical enitites of type dorsal telencephalic commissure phenotype",
                    "absent material anatomical entity in the brain",
                    "absent ectoderm-derived structure in the brain",
                    "nervous system commissure phenotype",
                    "absent commissure of telencephalon",
                    "corpus callosum morphology phenotype",
                    "number of anatomical enitites of type intercerebral commissure phenotype",
                    "tract of brain phenotype",
                    "white matter of telencephalon",
                    "brain white matter",
                    "tract of brain",
                    "absent corpus callosum",
                    "neural crest-derived structure phenotype",
                    "Aplasia/Hypoplasia of the corpus callosum",
                    "white matter phenotype",
                    "Abnormal cerebral white matter morphology",
                    "white matter of forebrain",
                    "abdomen element phenotype",
                    "U-shaped kidney",
                    "Horseshoe kidney",
                    "kidney phenotype",
                    "kidney morphology phenotype",
                    "shape of anatomical entity phenotype",
                    "3-D shape anatomical entity",
                    "Abnormal localization of kidney",
                    "intercerebral commissure phenotype",
                    "abdomen element",
                    "renal system morphology phenotype",
                    "kidney",
                    "reproductive structure phenotype",
                    "gland of diencephalon",
                    "decreased size of the gland",
                    "reproductive gland",
                    "corpus callosum",
                    "reproductive gland morphology phenotype",
                    "diencephalon morphology phenotype",
                    "hypothalamus-pituitary axis phenotype",
                    "decreased size of the reproductive organ",
                    "pituitary gland",
                    "diencephalon",
                    "endocrine system morphology phenotype",
                    "pituitary gland phenotype",
                    "reproductive gland phenotype",
                    "reproductive system morphology phenotype",
                    "Small pituitary gland",
                    "decreased size of the reproductive gland",
                    "decreased size of the pituitary gland",
                    "size of pituitary gland phenotype",
                    "endocrine gland morphology phenotype",
                    "reproductive structure",
                    "decreased size of the structure with developmental contribution from neural crest",
                    "gland morphology phenotype",
                    "gland of diencephalon phenotype",
                    "reproductive system phenotype",
                    "diencephalon phenotype",
                    "mesenchyme from somatopleure",
                    "decreased length of manual digit metacarpus endochondral element",
                    "decreased length of manual digit 1 phalanx endochondral element",
                    "metapodial skeleton phenotype",
                    "decreased length of forelimb long bone",
                    "paired limb/fin bud mesenchyme phenotype",
                    "ocular surface region morphology phenotype",
                    "Abnormality of thumb phalanx",
                    "decreased length of manual digit bone",
                    "decreased size of the autopod endochondral element",
                    "Aplasia/Hypoplasia of the phalanges of the thumb",
                    "decreased size of the phalanx",
                    "aplasia or hypoplasia of phalanx of manus",
                    "phalanx of manus phenotype",
                    "manus bone phenotype",
                    "metacarpal bone of digit 1",
                    "manual digitopodium bone",
                    "metapodium bone 1",
                    "metacarpal bone",
                    "Abnormality of the kidney",
                    "digitopodium bone",
                    "manus bone",
                    "aplasia or hypoplasia of metacarpal bone",
                    "decreased size of the autopod bone",
                    "phalanx endochondral element",
                    "manual digit phalanx endochondral element",
                    "manual digit metacarpus endochondral element",
                    "phalanx",
                    "autopod bone",
                    "decreased length of metapodium bone 1",
                    "decreased length of manual digit 1 metacarpus endochondral element",
                    "decreased length of manual digit phalanx endochondral element",
                    "manual digit bone phenotype",
                    "manual digit 1 metacarpus endochondral element phenotype",
                    "manual digit phalanx endochondral element phenotype",
                    "metapodial skeleton",
                    "metacarpal bone of digit 1 morphology phenotype",
                    "metacarpus skeleton",
                    "digit 1 digitopodial skeleton",
                    "manual digit digitopodial skeleton",
                    "metapodium region",
                    "phalanx endochondral element phenotype",
                    "metacarpal bone of digit 1 phenotype",
                    "decreased length of limb long bone",
                    "cartilage element phenotype",
                    "autopod endochondral element phenotype",
                    "aplasia or hypoplasia of metacarpal bone of digit 1",
                    "manual digit bone",
                    "cartilaginous condensation",
                    "material anatomical entity, curved phenotype",
                    "phalanx phenotype",
                    "decreased size of the digitopodium bone",
                    "decreased length of digitopodium bone",
                    "individual digit of digitopodial skeleton",
                    "skeleton of digitopodium",
                    "decreased length of phalanx of manus",
                    "anatomical entity morphology in the skeleton of manus phenotype",
                    "decreased length of metacarpal bone of digit 1",
                    "manual digit 1 phalanx endochondral element phenotype",
                    "Aplasia/Hypoplasia of the phalanges of the hand",
                    "decreased length of phalanx endochondral element",
                    "Aplasia/Hypoplasia of the 1st metacarpal",
                    "metacarpal bone phenotype",
                    "cardiac ventricle morphology phenotype",
                    "Ventricular septal defect",
                    "Abnormal ventricular septum morphology",
                    "cardiac ventricle",
                    "Anemia",
                    "erythrocyte",
                    "Short metacarpal",
                    "Abnormal erythrocyte morphology",
                    "Cafe-au-lait spot",
                    "pigmentation phenotype",
                    "metacarpal bone morphology phenotype",
                    "integument phenotype",
                    "cornea, curved phenotype",
                    "integumental system",
                    "Hyperpigmentation of the skin",
                    "skin of body",
                    "septum of telencephalon",
                    "increased pigmentation in skin of body",
                    "Irregular hyperpigmentation",
                    "Macule",
                    "increased qualitatively biological_process",
                    "increased biological_process in skin of body",
                    "skin of body phenotype",
                    "increased biological_process",
                    "skin of body morphology phenotype",
                    "Localized skin lesion",
                    "nervous system commissure",
                    "bone marrow",
                    "Abnormal bone marrow cell morphology",
                    "Abnormality of multiple cell lineages in the bone marrow",
                    "blood vessel",
                    "coronary vessel",
                    "systemic artery morphology phenotype",
                    "number of anatomical enitites of type brain commissure phenotype",
                    "Abnormal blood vessel morphology",
                    "Abnormality of the vasculature",
                    "blood vessel phenotype",
                    "absent lamina",
                    "vasculature",
                    "artery morphology phenotype",
                    "incomplete closing of the systemic artery",
                    "systemic artery",
                    "incomplete closing of the ductus arteriosus",
                    "coronary vessel morphology phenotype",
                    "vessel",
                    "outflow tract",
                    "great vessel of heart phenotype",
                    "vasculature of organ phenotype",
                    "multicellular anatomical structure morphology in the heart phenotype",
                    "vasculature phenotype",
                    "thoracic segment blood vessel",
                    "number of anatomical enitites of type multi cell part structure phenotype",
                    "artery",
                    "systemic arterial system",
                    "incomplete closing of the thoracic segment blood vessel",
                    "artery phenotype",
                    "reproductive system",
                    "incomplete closing of the blood vessel",
                    "Patent ductus arteriosus",
                    "skeleton of manual digitopodium",
                    "arterial blood vessel phenotype",
                    "incomplete closing of the artery",
                    "incomplete closing of the coronary vessel",
                    "systemic artery phenotype",
                    "brain commissure phenotype",
                    "trunk blood vessel",
                    "arterial blood vessel",
                    "great vessel of heart",
                    "heart blood vessel",
                    "incomplete closing of the heart blood vessel",
                    "erythrocyte morphology phenotype",
                    "vascular system morphology phenotype",
                    "Congenital malformation of the great arteries",
                    "number of anatomical enitites of type central nervous system cell part cluster phenotype",
                    "blood vasculature",
                    "outflow tract phenotype",
                    "number of anatomical enitites of type commissure of telencephalon phenotype",
                    "ductus arteriosus morphology phenotype",
                    "conceptus",
                    "anatomical conduit atresia",
                    "external ear morphology phenotype",
                    "closing of the ectoderm-derived structure",
                    "Abnormality of the outer ear",
                    "external acoustic meatus phenotype",
                    "external acoustic meatus morphology phenotype",
                    "endoderm-derived structure atresia",
                    "external ear phenotype",
                    "closing of the endoderm-derived structure",
                    "Abnormal auditory canal morphology",
                    "Atresia of the external auditory canal",
                    "manual digit 1 metacarpus endochondral element",
                    "Abnormal skull morphology",
                    "Decreased head circumference",
                    "size of skull phenotype",
                    "cranial skeletal system",
                    "skull",
                    "anatomical structure, curved phenotype",
                    "Microcephaly",
                    "cerebral hemisphere white matter",
                    "Aplasia/Hypoplasia of the cerebrum",
                    "Abnormal cerebral morphology",
                    "abdominal segment of trunk",
                    "excretory tube",
                    "abdominal segment element",
                    "lower urinary tract phenotype",
                    "Abnormality of the genitourinary system",
                    "mesoderm-derived structure physiology phenotype",
                    "renal pelvis/ureter",
                    "bladder organ phenotype",
                    "bladder organ physiology phenotype",
                    "Abnormality of the lower urinary tract",
                    "external ear",
                    "Abnormality of the bladder",
                    "metacarpus skeleton phenotype",
                    "urinary bladder physiology phenotype",
                    "Abnormal ureter physiology",
                    "Functional abnormality of the bladder",
                    "lower urinary tract",
                    "ectoderm-derived structure, curved phenotype",
                    "renal system",
                    "excretory tube phenotype",
                    "sac physiology phenotype",
                    "cavitated compound organ physiology phenotype",
                    "Abnormality of the upper urinary tract",
                    "sac phenotype",
                    "compound organ physiology phenotype",
                    "pelvic region element",
                    "pelvic region of trunk",
                    "bladder organ",
                    "urinary bladder",
                    "genitourinary system",
                    "cartilage element",
                    "excretory system",
                    "cavitated compound organ phenotype",
                    "renal system phenotype",
                    "ureter",
                    "upper urinary tract",
                    "genitourinary system phenotype",
                    "Abnormal metacarpal morphology",
                    "viscus physiology phenotype",
                    "ureter physiology phenotype",
                    "renal/urinary system phenotype",
                    "ventricular system of brain",
                    "ventricle of nervous system phenotype",
                    "telencephalic ventricle",
                    "brain ventricle morphology phenotype",
                    "brain ventricle/choroid plexus phenotype",
                    "forebrain morphology phenotype",
                    "forebrain",
                    "telencephalon",
                    "Colpocephaly",
                    "Abnormal lateral ventricle morphology",
                    "telencephalic ventricle morphology phenotype",
                    "brain ventricle/choroid plexus",
                    "Abnormal cerebral ventricle morphology",
                    "skull phenotype",
                    "anterior neural tube",
                    "telencephalon phenotype",
                    "programmed DNA elimination by chromosome breakage",
                    "programmed DNA elimination by chromosome breakage phenotype",
                    "Chromosomal breakage induced by crosslinking agents",
                    "homeostatic process phenotype",
                    "negative regulation of gene expression phenotype",
                    "absent neuron projection bundle",
                    "absent central nervous system cell part cluster",
                    "regulation of gene expression",
                    "Abnormal cellular phenotype",
                    "Abnormal cellular physiology",
                    "gene expression phenotype",
                    "U-shaped anatomical entity",
                    "macromolecule biosynthetic process phenotype",
                    "metabolic process phenotype",
                    "great vessel of heart morphology phenotype",
                    "negative regulation of cellular process",
                    "programmed DNA elimination",
                    "negative regulation of gene expression",
                    "negative regulation of biological process",
                    "biosynthetic process",
                    "macromolecule metabolic process",
                    "Chromosome breakage",
                    "homeostatic process",
                    "regulation of cellular process",
                    "small intestine",
                    "neural crest-derived structure, curved phenotype",
                    "Abnormal platelet count",
                    "absent anatomical structure in the brain ventricle",
                    "intestine",
                    "Abnormal cardiac ventricle morphology",
                    "alimentary part of gastrointestinal system atresia",
                    "number of cell phenotype",
                    "Abnormality of the digestive system",
                    "absent material anatomical entity in the tissue",
                    "decreased functionality of the thyroid gland",
                    "subdivision of tube",
                    "subdivision of digestive tract",
                    "abdomen",
                    "developing anatomical structure phenotype",
                    "intestine morphology phenotype",
                    "Abnormal renal morphology",
                    "anatomical entity perforation",
                    "closing of the anatomical entity",
                    "multicellular anatomical structure atresia",
                    "cell condensation",
                    "closing of the anatomical structure",
                    "alimentary part of gastrointestinal system morphology phenotype",
                    "anterior lateral plate mesoderm",
                    "arm bone phenotype",
                    "erythroid lineage cell",
                    "limb bud morphology phenotype",
                    "Short 1st metacarpal",
                    "formed anatomical structure",
                    "appendicular skeletal system",
                    "Synostosis of joints",
                    "forelimb long bone phenotype",
                    "decreased length of forelimb zeugopod bone",
                    "appendicular skeleton morphology phenotype",
                    "Abnormal forearm bone morphology",
                    "decreased size of the mesoderm-derived structure",
                    "anatomical entity morphology in the alimentary part of gastrointestinal system phenotype",
                    "bone element phenotype",
                    "digit phenotype",
                    "reproductive organ phenotype",
                    "heart vasculature",
                    "Abnormal morphology of the radius",
                    "Abnormality of the ureter",
                    "gene expression",
                    "vessel phenotype",
                    "skeleton of pectoral complex",
                    "Abnormality of the curvature of the cornea",
                    "metapodium bone",
                    "skeletal system",
                    "subdivision of skeletal system",
                    "alimentary part of gastrointestinal system",
                    "Aplasia/hypoplasia involving forearm bones",
                    "incomplete closing of the cardiac septum",
                    "occurrent",
                    "fused cervical vertebra and cervical vertebra",
                    "external acoustic meatus atresia",
                    "decreased size of the bone of appendage girdle complex",
                    "appendage girdle complex",
                    "cell communication",
                    "forelimb zeugopod",
                    "closing of the multicellular anatomical structure",
                    "forelimb bone",
                    "limb bone morphology phenotype",
                    "abdominal segment element phenotype",
                    "anatomical entity morphology in the appendage girdle complex phenotype",
                    "absent tissue in the multicellular organism",
                    "peptide hormone secretion",
                    "manual digitopodium bone phenotype",
                    "anatomical entity hypoplasia",
                    "forelimb zeugopod phenotype",
                    "Abnormality of the integument",
                    "anatomical structure development",
                    "forelimb zeugopod morphology phenotype",
                    "eyeball of camera-type eye",
                    "limb bone phenotype",
                    "Abnormal forearm morphology",
                    "system",
                    "Neurodevelopmental abnormality",
                    "upper urinary tract phenotype",
                    "manual digit 1 or 5",
                    "migrating mesenchyme population",
                    "forelimb bud phenotype",
                    "skeleton of limb phenotype",
                    "Abnormality of joint mobility",
                    "Abnormal finger phalanx morphology",
                    "decreased length of forelimb bone",
                    "decreased size of the endochondral element",
                    "bone of appendage girdle complex phenotype",
                    "Abnormality of the ear",
                    "forelimb zeugopod skeleton",
                    "Abnormality of body weight",
                    "absent limb endochondral element in the limb",
                    "manual digit 1 plus metapodial segment",
                    "regulation of hormone levels phenotype",
                    "cartilaginous condensation phenotype",
                    "bone of pectoral complex",
                    "camera-type eye physiology phenotype",
                    "skeleton phenotype",
                    "arm phenotype",
                    "decreased qualitatively embryo development",
                    "camera-type eye phenotype",
                    "blastula",
                    "Abnormal morphology of the great vessels",
                    "cranial neuron projection bundle",
                    "decreased length of organ",
                    "surface structure phenotype",
                    "decreased size of the bone of pectoral complex",
                    "digestive system",
                    "vertebra",
                    "mesoderm-derived structure",
                    "radius bone morphology phenotype",
                    "limb",
                    "Abnormality of the middle ear",
                    "anatomical entity atresia",
                    "decreased qualitatively sensory perception of mechanical stimulus",
                    "pectoral appendage",
                    "decreased length of bone element",
                    "radius bone hypoplasia",
                    "articulation",
                    "decreased length of limb endochondral element",
                    "Aplasia/Hypoplasia involving the metacarpal bones",
                    "heart tube",
                    "Abnormality of head or neck",
                    "aplasia or hypoplasia of cranial nerve II",
                    "anatomical entity morphology in the pectoral complex phenotype",
                    "sensory perception phenotype",
                    "Aplasia/hypoplasia involving bones of the upper limbs",
                    "body proper",
                    "myeloid leukocyte",
                    "dense mesenchyme tissue",
                    "pectoral appendage skeleton",
                    "anatomical structure atresia",
                    "aplastic anatomical entity",
                    "multi organ part structure physiology phenotype",
                    "anatomical entity physiology phenotype",
                    "digestive system morphology phenotype",
                    "decreased length of arm bone",
                    "autopod region phenotype",
                    "closing of the anatomical system",
                    "pectoral appendage bud phenotype",
                    "number of anatomical enitites of type endochondral element phenotype",
                    "ventricular system of central nervous system",
                    "decreased size of the anatomical entity",
                    "decreased size of the forelimb endochondral element",
                    "central nervous system morphology phenotype",
                    "zeugopodial skeleton",
                    "arm",
                    "subdivision of tube atresia",
                    "limb morphology phenotype",
                    "Abnormality of limb bone",
                    "alimentary part of gastrointestinal system phenotype",
                    "long bone",
                    "epithelial tube phenotype",
                    "endochondral bone",
                    "decreased length of metacarpal bone",
                    "Abnormal upper limb bone morphology",
                    "autopod endochondral element",
                    "Abnormal duodenum morphology",
                    "asymmetrically curved anatomical entity",
                    "endochondral element phenotype",
                    "limb segment phenotype",
                    "incomplete closing of the vessel",
                    "appendage phenotype",
                    "decreased size of the long bone",
                    "ectoderm-derived structure phenotype",
                    "organ subunit phenotype",
                    "Abnormal immune system morphology",
                    "tissue",
                    "absent material anatomical entity",
                    "concave 3-D shape anatomical entity",
                    "decreased length of multicellular anatomical structure",
                    "absent anatomical structure in the brain",
                    "interatrial septum perforation",
                    "decreased size of the arm bone",
                    "aplasia or hypoplasia of anatomical entity",
                    "musculoskeletal system phenotype",
                    "decreased size of the material anatomical entity in the pectoral complex",
                    "Abnormal gastrointestinal tract morphology",
                    "Abnormality of the skeletal system",
                    "decreased size of the phalanx endochondral element",
                    "optic cup morphology phenotype",
                    "regulation of biological process",
                    "secretion phenotype",
                    "paired limb/fin skeleton phenotype",
                    "forelimb phenotype",
                    "bone of free limb or fin phenotype",
                    "appendicular skeleton",
                    "limb skeleton subdivision phenotype",
                    "decreased size of the limb endochondral element",
                    "pituitary gland morphology phenotype",
                    "Absent forearm bone",
                    "digit 1 plus metapodial segment",
                    "absent limb endochondral element",
                    "Abnormality of the upper limb",
                    "orbital region phenotype",
                    "anatomical structure morphology in the heart phenotype",
                    "skeletal system morphology phenotype",
                    "endochondral element",
                    "skeletal joint morphology phenotype",
                    "bone element",
                    "regulation of metabolic process",
                    "subdivision of organism along appendicular axis",
                    "small intestine morphology phenotype",
                    "forelimb zeugopod bone",
                    "macromolecule biosynthetic process",
                    "skeletal element",
                    "decreased size of the multicellular anatomical structure in the pectoral complex",
                    "limb segment",
                    "paired limb/fin",
                    "duodenum",
                    "paired limb/fin phenotype",
                    "anatomical entity dysfunction in independent continuant",
                    "paired limb/fin bud phenotype",
                    "decreased size of the multicellular anatomical structure",
                    "somite",
                    "aplasia or hypoplasia of skeleton",
                    "neural crest-derived structure",
                    "Abnormal granulocyte count",
                    "number of anatomical enitites of type neutrophil phenotype",
                    "regulation of biological quality",
                    "subdivision of tube phenotype",
                    "lateral structure",
                    "entire sense organ system",
                    "decreased size of the anatomical structure",
                    "absent anatomical entity in the limb",
                    "skull morphology phenotype",
                    "manual digit",
                    "skeleton of manus",
                    "zeugopod phenotype",
                    "unilaminar epithelium phenotype",
                    "bone of dorsum phenotype",
                    "ectoderm",
                    "paired limb/fin bud",
                    "limb endochondral element",
                    "neural plate",
                    "decreased qualitatively sensory perception",
                    "anatomical entity length phenotype",
                    "decreased length of bone of free limb or fin",
                    "decreased size of the material anatomical entity",
                    "pectoral appendage bud",
                    "central nervous system phenotype",
                    "neutrophil",
                    "formed multi-tissue structure",
                    "sclerotome",
                    "vision/eye phenotype",
                    "aplasia or hypoplasia of eyeball of camera-type eye",
                    "neural plate phenotype",
                    "absent bone of pectoral complex in the limb",
                    "organ system subdivision",
                    "visual system phenotype",
                    "decreased number of material anatomical entity",
                    "photoreceptor array phenotype",
                    "subdivision of digestive tract phenotype",
                    "absent endochondral element",
                    "nervous system",
                    "dorsum",
                    "Abnormality of refraction",
                    "absent endochondral bone in the forelimb",
                    "embryonic cardiovascular system",
                    "Absent thumb",
                    "multicellular anatomical structure physiology phenotype",
                    "Abnormal thumb morphology",
                    "long bone morphology phenotype",
                    "decreased size of the multicellular organism",
                    "limb long bone",
                    "organ physiology phenotype",
                    "absent ectoderm-derived structure",
                    "simple eye physiology phenotype",
                    "Limb undergrowth",
                    "decreased qualitatively biological_process",
                    "musculature of body",
                    "number of anatomical enitites of type organism subdivision phenotype",
                    "eye physiology phenotype",
                    "epithelium",
                    "thoracic cavity element",
                    "subdivision of skeleton",
                    "anatomical entity phenotype",
                    "absent organ in the tissue",
                    "lateral plate mesoderm",
                    "absent autopodial extension",
                    "heart tube morphology phenotype",
                    "axial skeleton plus cranial skeleton phenotype",
                    "incomplete closing of the mesoderm-derived structure",
                    "anatomical system atresia",
                    "heart morphology phenotype",
                    "Abnormal ear morphology",
                    "presumptive structure",
                    "absent forelimb bone",
                    "decreased length of long bone",
                    "immature eye phenotype",
                    "zeugopod",
                    "anatomical system phenotype",
                    "anatomical entity morphology phenotype",
                    "multi-limb segment region phenotype",
                    "axon tract phenotype",
                    "forelimb skeleton phenotype",
                    "middle ear physiology phenotype",
                    "decreased number of neutrophil",
                    "incomplete closing of the material anatomical entity",
                    "subdivision of trunk phenotype",
                    "cranial skeletal system phenotype",
                    "future central nervous system phenotype",
                    "transport",
                    "heart plus pericardium",
                    "Forearm undergrowth",
                    "cardiac atrium phenotype",
                    "Decreased anatomical entity mass",
                    "septum phenotype",
                    "peptide transport phenotype",
                    "trunk region element",
                    "digestive system phenotype",
                    "multicellular organism morphology phenotype",
                    "decreased vibrational conductance of sound to the inner ear",
                    "tube",
                    "digitopodium region",
                    "vertebra morphology phenotype",
                    "cardiopharyngeal field",
                    "digit",
                    "developmental process phenotype",
                    "pre-chordal neural plate",
                    "intestine phenotype",
                    "cerebral hemisphere morphology phenotype",
                    "Abnormal limb bone morphology",
                    "neurectoderm",
                    "cardiac chamber phenotype",
                    "size of eyeball of camera-type eye phenotype",
                    "embryonic tissue phenotype",
                    "duodenum phenotype",
                    "blood",
                    "decreased size of the limb bone",
                    "germ layer phenotype",
                    "anatomical conduit",
                    "decreased length of autopodial extension",
                    "multi-tissue structure",
                    "circulatory system phenotype",
                    "organ part phenotype",
                    "absent anatomical structure in the limb",
                    "organ",
                    "incomplete closing of the anatomical structure",
                    "Abnormal cardiac septum morphology",
                    "endochondral bone phenotype",
                    "autopod region",
                    "white matter of forebrain phenotype",
                    "Abnormal myeloid leukocyte morphology",
                    "regulation of hormone levels",
                    "Abnormality of limbs",
                    "anatomical conduit phenotype",
                    "shape of continuant phenotype",
                    "mesenchyme morphology phenotype",
                    "forelimb morphology phenotype",
                    "decreased number of platelet",
                    "subdivision of trunk",
                    "ectoderm phenotype",
                    "integumental system phenotype",
                    "organ phenotype",
                    "tube phenotype",
                    "aplastic forelimb zeugopod bone",
                    "retina morphology phenotype",
                    "ecto-epithelium phenotype",
                    "autopodial extension",
                    "phenotype",
                    "negative regulation of macromolecule biosynthetic process",
                    "Patent foramen ovale",
                    "Abnormal posterior eye segment morphology",
                    "Abnormality of the hypothalamus-pituitary axis",
                    "main body axis",
                    "small intestine phenotype",
                    "Microphthalmia",
                    "mesenchyme",
                    "digestive tract",
                    "forelimb long bone",
                    "non-connected functional system",
                    "mesoderm-derived structure morphology in the heart phenotype",
                    "number of anatomical enitites of type material anatomical entity phenotype",
                    "decreased size of the anatomical entity in the pectoral complex",
                    "absent limb long bone in the forelimb",
                    "autopod bone phenotype",
                    "musculoskeletal system",
                    "limb bud",
                    "fused anatomical entity and vertebra",
                    "multicellular organism phenotype",
                    "simple eye phenotype",
                    "subdivision of head phenotype",
                    "forelimb bone phenotype",
                    "anterior region of body",
                    "subdivision of organism along main body axis phenotype",
                    "decreased size of the ectoderm-derived structure",
                    "developing mesenchymal condensation phenotype",
                    "cardiovascular system phenotype",
                    "cardiac atrium morphology phenotype",
                    "mesenchyme from somatopleure phenotype",
                    "Conductive hearing impairment",
                    "Abnormal intestine morphology",
                    "anatomical system physiology phenotype",
                    "formed regional part of brain",
                    "secretion by cell",
                    "material anatomical entity",
                    "Abnormal 1st metacarpal morphology",
                    "forelimb endochondral element",
                    "primary circulatory organ",
                    "migrating mesenchyme population phenotype",
                    "closing of the material anatomical entity",
                    "cardiovascular system morphology phenotype",
                    "cervical region",
                    "Intestinal atresia",
                    "meso-epithelium phenotype",
                    "cell-cell signaling",
                    "forebrain phenotype",
                    "decreased size of the forelimb bone",
                    "vertebral element",
                    "decreased length of skeletal element",
                    "gray matter phenotype",
                    "multicellular organism",
                    "absent nervous system commissure",
                    "decreased length of forelimb endochondral element",
                    "Atrial septal defect",
                    "decreased multicellular anatomical structure mass",
                    "organ part",
                    "cerebral hemisphere white matter morphology phenotype",
                    "size of anatomical entity phenotype",
                    "anlage",
                    "sense organ",
                    "anatomical system",
                    "hypothalamus-pituitary axis",
                    "forelimb zeugopod bone phenotype",
                    "heart primordium phenotype",
                    "Absent septum pellucidum",
                    "Abnormal pituitary gland morphology",
                    "Abnormality of the urinary system",
                    "number of leukocyte phenotype",
                    "cardiac atrium",
                    "Vertebral fusion",
                    "multicellular anatomical structure",
                    "process",
                    "formed ectoderm-derived structure",
                    "subdivision of head",
                    "decreased size of the digit",
                    "All",
                    "lateral plate mesoderm phenotype",
                    "cerebral subcortex",
                    "epithelial tube",
                    "skeletal system phenotype",
                    "Abnormality of the gastrointestinal tract",
                    "cardiogenic splanchnic mesoderm",
                    "Bone marrow hypocellularity",
                    "heart primordium",
                    "multi-tissue structure phenotype",
                    "decreased length of metapodium bone",
                    "Abnormal cellular immune system morphology",
                    "decreased length of bone of pectoral complex",
                    "mesoderm phenotype",
                    "decreased length of autopod bone",
                    "biological_process",
                    "immune system morphology phenotype",
                    "manus morphology phenotype",
                    "primary heart field phenotype",
                    "axon tract morphology phenotype",
                    "independent continuant",
                    "cardiac septum",
                    "Abnormal growth hormone level",
                    "Abnormality of the cardiovascular system",
                    "decreased length of bone of appendage girdle complex",
                    "Abnormality of the head",
                    "decreased size of the endochondral bone",
                    "granulocyte",
                    "organ part atresia",
                    "Functional abnormality of the middle ear",
                    "interventricular septum morphology phenotype",
                    "cervical vertebra endochondral element",
                    "simple eye",
                    "primary heart field",
                    "anatomical structure phenotype",
                    "absent bone of pectoral complex",
                    "face",
                    "heart phenotype",
                    "subdivision of digestive tract atresia",
                    "embryo phenotype",
                    "cardiac chamber",
                    "epithelium phenotype",
                    "Abnormal heart morphology",
                    "absent mesoderm-derived structure in the limb",
                    "Short long bone",
                    "organism subdivision phenotype",
                    "cerebellum morphology phenotype",
                    "decreased size of the anatomical structure in the pectoral complex",
                    "neck bone phenotype",
                    "bone of pectoral complex morphology phenotype",
                    "interventricular septum",
                    "Abnormality of neutrophils",
                    "localization",
                    "neural tube morphology phenotype",
                    "subdivision of organism along main body axis",
                    "germ layer morphology phenotype",
                    "Short stature",
                    "tissue phenotype",
                    "Short finger",
                    "limb phenotype",
                    "embryonic structure",
                    "decreased length of phalanx",
                    "anatomical entity",
                    "anatomical entity morphology in the heart phenotype",
                    "digestive system element",
                    "aplasia or hypoplasia of radius bone",
                    "Short phalanx of the thumb",
                    "germ layer / neural crest",
                    "embryo morphology phenotype",
                    "Opisthokonta",
                    "Abnormal vascular morphology",
                    "pelvic region element phenotype",
                    "hormone transport",
                    "orbital region",
                    "limb skeleton subdivision",
                    "Phenotypic abnormality",
                    "hematopoietic system",
                    "anatomical structure",
                    "malformed anatomical entity",
                    "decreased size of the limb long bone",
                    "limb bone",
                    "eye phenotype",
                    "Abnormal brain morphology",
                    "cardiovascular system",
                    "ear phenotype",
                    "interatrial septum",
                    "anatomical entity morphology in the skeleton of pectoral complex phenotype",
                    "gastrula morphology phenotype",
                    "face phenotype",
                    "blood vessel morphology phenotype",
                    "regional part of nervous system phenotype",
                    "Hearing impairment",
                    "splanchnic layer of lateral plate mesoderm phenotype",
                    "number of anatomical enitites of type neuron projection bundle phenotype",
                    "entity",
                    "disconnected anatomical group",
                    "absent dorsal telencephalic commissure",
                    "bone of pectoral complex phenotype",
                    "metabolic process",
                    "decreased length of manual digitopodium bone",
                    "decreased length of autopod endochondral element",
                    "phenotypic effect",
                    "gray matter",
                    "embryo development rate phenotype",
                    "developing anatomical structure",
                    "multicellular anatomical structure phenotype",
                    "cardiac septum morphology phenotype",
                    "absent forelimb endochondral element",
                    "Aplasia/Hypoplasia affecting the eye",
                    "amide transport",
                    "immature eye",
                    "skeleton",
                    "presumptive structure phenotype",
                    "skeletal element phenotype",
                    "decreased length of anatomical entity",
                    "mesenchyme phenotype",
                    "endoderm-derived structure",
                    "decreased length of mesoderm-derived structure",
                    "dense mesenchyme tissue phenotype",
                    "forelimb endochondral element phenotype",
                    "manual digit 1 phalanx phenotype",
                    "craniofacial/craniocervical phenotype",
                    "agenesis of anatomical entity",
                    "anlage phenotype",
                    "trunk",
                    "cervical vertebra morphology phenotype",
                    "Abnormal forebrain morphology",
                    "cardiogenic plate morphology phenotype",
                    "embryonic tissue",
                    "decreased number of cell",
                    "absent organ in the limb",
                    "bone of free limb or fin",
                    "camera-type eye",
                    "absent mesoderm-derived structure",
                    "cell phenotype",
                    "absent brain commissure",
                    "paired limb/fin bud mesenchyme",
                    "pectoral appendage phenotype",
                    "Abnormal finger morphology",
                    "material anatomical entity phenotype",
                    "future nervous system",
                    "structure with developmental contribution from neural crest, asymmetrically curved phenotype",
                    "sensory perception",
                    "structure with developmental contribution from neural crest phenotype",
                    "decreased length of manus bone",
                    "Abnormal cardiac atrium morphology",
                    "bone of appendage girdle complex",
                    "decreased size of the forelimb zeugopod bone",
                    "trunk region element phenotype",
                    "circulatory organ",
                    "Aplasia/hypoplasia involving bones of the extremities",
                    "decreased size of the organ",
                    "Abnormality of the vertebral column",
                    "heart",
                    "erythroid lineage cell morphology phenotype",
                    "middle ear",
                    "lateral plate mesoderm morphology phenotype",
                    "skeleton of limb",
                    "organ system subdivision phenotype",
                    "pigmentation",
                    "radius endochondral element",
                    "compound organ",
                    "primordium",
                    "urinary bladder phenotype",
                    "viscus",
                    "Duodenal atresia",
                    "head",
                    "trunk mesenchyme phenotype",
                    "establishment of localization",
                    "Reduced circulating growth hormone concentration",
                    "fused skeletal joint and anatomical entity",
                    "structure with developmental contribution from neural crest",
                    "thoracic segment of trunk",
                    "material anatomical entity physiology phenotype",
                    "subdivision of skeletal system phenotype",
                    "incomplete closing of the anatomical entity",
                    "cardiac septum phenotype",
                    "myeloid leukocyte phenotype",
                    "Abnormal fundus morphology",
                    "eye primordium",
                    "organ component layer phenotype",
                    "phalanx of manus",
                    "number of hematopoietic cell phenotype",
                    "continuant",
                    "viscus phenotype",
                    "forelimb zeugopod bone morphology phenotype",
                    "cell",
                    "forelimb",
                    "forelimb bud",
                    "lateral structure phenotype",
                    "brain ventricle",
                    "material anatomical entity morphology in the heart phenotype",
                    "nucleate cell",
                    "absent multi cell part structure",
                    "material anatomical entity atresia",
                    "heart tube phenotype",
                    "metencephalon",
                    "long bone phenotype",
                    "motile cell",
                    "integument",
                    "gland",
                    "trunk region element physiology phenotype",
                    "upper limb segment phenotype",
                    "compound organ phenotype",
                    "craniocervical region phenotype",
                    "establishment of localization phenotype",
                    "germ layer",
                    "eukaryotic cell",
                    "Abnormal total neutrophil count",
                    "Abnormality of the face",
                    "postcranial axial skeleton",
                    "blood cell",
                    "decreased size of the reproductive structure",
                    "Abnormality of thyroid physiology",
                    "paired limb/fin segment",
                    "anatomical structure physiology phenotype",
                    "decreased length of manual digit 1 phalanx",
                    "decreased number of anatomical entity",
                    "number of myeloid cell phenotype",
                    "number of anatomical enitites of type granulocyte phenotype",
                    "secretory cell",
                    "Abnormality of blood and blood-forming tissues",
                    "vibrational conductance of sound to the inner ear",
                    "absent anatomical entity in the central nervous system",
                    "posterior neural tube",
                    "Abnormal granulocyte morphology",
                    "Abnormal ear physiology",
                    "presumptive paraxial mesoderm",
                    "shape of kidney phenotype",
                    "limb long bone morphology phenotype",
                    "myeloid cell",
                    "cardiogenic splanchnic mesoderm phenotype",
                    "subdivision of skeleton phenotype",
                    "blood cell phenotype",
                    "decreased qualitatively multicellular organismal process",
                    "optic disc morphology phenotype",
                    "metacarpus region",
                    "leukocyte",
                    "appendicular skeleton phenotype",
                    "Abnormal small intestine morphology",
                    "immune system phenotype",
                    "hematopoietic system phenotype",
                    "opening of the anatomical entity",
                    "asymmetrically curved cornea",
                    "digitopodium bone phenotype",
                    "duodenum atresia",
                    "decreased number of myeloid cell",
                    "granulocyte morphology phenotype",
                    "decreased size of the eyeball of camera-type eye",
                    "immune system",
                    "Aplasia/Hypoplasia of the radius",
                    "Decreased total neutrophil count",
                    "Abnormal leukocyte count",
                    "embryo",
                    "future central nervous system",
                    "leukocyte morphology phenotype",
                    "pre-chordal neural plate phenotype",
                    "decreased length of limb bone",
                    "thoracic segment organ phenotype",
                    "limb endochondral element phenotype",
                    "Abnormality of the immune system",
                    "neutrophil phenotype",
                    "decreased number of anatomical structure",
                    "arm bone",
                    "upper limb segment",
                    "incomplete closing of the interatrial septum",
                    "craniocervical region",
                    "decreased size of the manus bone",
                    "Triangular face",
                    "decreased size of the organism subdivision",
                    "head phenotype",
                    "limb bud phenotype",
                    "eyeball of camera-type eye phenotype",
                    "incomplete closing of the arterial blood vessel",
                    "surface structure",
                    "sense organ physiology phenotype",
                    "appendage",
                    "ear",
                    "neurectoderm phenotype",
                    "organism subdivision",
                    "chemical entity",
                    "Myopia",
                    "eye",
                    "sense organ phenotype",
                    "absent anatomical entity in the nervous system",
                    "ureter phenotype",
                    "duodenum morphology phenotype",
                    "visual system",
                    "incomplete closing of the anatomical conduit",
                    "brain morphology phenotype",
                    "digestive system element phenotype",
                    "irregular bone",
                    "sensory system",
                    "pectoral appendage skeleton phenotype",
                    "ectoderm-derived structure",
                    "primary circulatory organ phenotype",
                    "hemolymphoid system",
                    "sensory system phenotype",
                    "endocrine system",
                    "system process",
                    "unilaminar epithelium",
                    "taxon specific phenotype",
                    "epithelial vesicle phenotype",
                    "digit 1 or 5 phenotype",
                    "decreased length of endochondral element",
                    "forelimb bud morphology phenotype",
                    "Abnormal joint morphology",
                    "absent anatomical entity in the brain",
                    "increased pigmentation",
                    "presumptive ectoderm phenotype",
                    "multi organ part structure phenotype",
                    "bone cell",
                    "ecto-epithelium",
                    "Abnormal digestive system morphology",
                    "multicellular organism mass phenotype",
                    "Abnormality of skull size",
                    "intestine atresia",
                    "absent limb bone in the forelimb",
                    "Aplasia/Hypoplasia involving the central nervous system",
                    "absent forelimb endochondral element in the forelimb",
                    "dorsal region element phenotype",
                    "absent organ",
                    "axial skeleton plus cranial skeleton morphology phenotype",
                    "embryo development",
                    "septum",
                    "decreased sensory perception",
                    "cervical vertebra",
                    "absent radius bone",
                    "manual digit 1 phalanx endochondral element",
                    "posterior segment of eyeball",
                    "number of anatomical enitites of type endochondral bone phenotype",
                    "number of anatomical enitites of type organ phenotype",
                    "absent forelimb zeugopod bone",
                    "absent bone of free limb or fin",
                    "decreased number of hematopoietic cell",
                    "absent bone element",
                    "material entity",
                    "splanchnic layer of lateral plate mesoderm",
                    "absent material anatomical entity in the limb bud",
                    "cervical vertebra phenotype",
                    "incomplete closing of the trunk blood vessel",
                    "Short neck",
                    "reproductive organ",
                    "absent anatomical entity in the tissue",
                    "sclerotome morphology phenotype",
                    "metencephalon morphology phenotype",
                    "cervical vertebra endochondral element phenotype",
                    "absent bone element in the limb",
                    "Upper limb undergrowth",
                    "absent multicellular anatomical structure in the limb",
                    "absent material anatomical entity in the limb",
                    "closing of the anatomical conduit",
                    "germ layer / neural crest phenotype",
                    "number of anatomical enitites of type multicellular anatomical structure phenotype",
                    "intercerebral commissure",
                    "absent multicellular anatomical structure in the tissue",
                    "absent anatomical structure in the forelimb",
                    "absent radius endochondral element",
                    "regional part of brain phenotype",
                    "absent forelimb zeugopod bone in the forelimb",
                    "paraxial mesoderm morphology phenotype",
                    "decreased functionality of the material anatomical entity",
                    "Short digit",
                    "limb long bone phenotype",
                    "chordal neural plate phenotype",
                    "absent mesoderm-derived structure in the forelimb",
                    "absent bone element in the forelimb",
                    "embryonic tissue morphology phenotype",
                    "absent anatomical entity in the multicellular organism",
                    "absent multicellular anatomical structure in the multicellular organism",
                    "absent multicellular anatomical structure in the skeletal system",
                    "trunk blood vessel phenotype",
                    "absent forelimb long bone in the forelimb",
                    "digit plus metapodial segment",
                    "absent anatomical entity in the limb bud",
                    "cornea morphology phenotype",
                    "absent anatomical entity",
                    "number of anatomical enitites of type bone element phenotype",
                    "Abnormal cerebellum morphology",
                    "absent multicellular anatomical structure in the forelimb",
                    "sensory perception of sound phenotype",
                    "absent arm bone in the forelimb",
                    "absent anatomical structure in the skeletal system",
                    "decreased qualitatively developmental process",
                    "absent bone of free limb or fin in the limb",
                    "absent radius endochondral element in the forelimb",
                    "absent limb bone in the limb",
                    "absent bone of appendage girdle complex",
                    "Absent radius",
                    "decreased size of the gland of diencephalon",
                    "skeleton of manual acropodium",
                    "articular system",
                    "Abnormal cerebral subcortex morphology",
                    "absent limb bone",
                    "manual digit 1 digitopodial skeleton",
                    "anatomical wall",
                    "absent material anatomical entity in the forelimb",
                    "absent limb long bone",
                    "absent endochondral bone in the limb",
                    "decreased size of the skeletal element",
                    "autopod region morphology phenotype",
                    "vasculature of trunk",
                    "absent anatomical entity in the forelimb",
                    "absent material anatomical entity in the multicellular organism",
                    "radius bone",
                    "digit 1 or 5",
                    "absent anatomical structure in the tissue",
                    "absent forelimb bone in the forelimb",
                    "absent arm bone",
                    "arterial system",
                    "cavitated compound organ",
                    "Aplasia involving forearm bones",
                    "formed cerebellum",
                    "absent forelimb bone in the limb",
                    "Abnormality of the musculoskeletal system",
                    "absent long bone",
                    "segment of autopod",
                    "absent skeletal element",
                    "absent forelimb long bone",
                    "absent organ in the multicellular organism",
                    "number of anatomical enitites of type nervous system commissure phenotype",
                    "amide transport phenotype",
                    "absent skeletal element in the limb",
                    "absent multicellular anatomical structure",
                    "absent anatomical entity in the skeletal system",
                    "decreased embryo development",
                    "absent bone of appendage girdle complex in the limb",
                    "absent material anatomical entity in the skeletal system",
                    "anatomical cluster phenotype",
                    "absent anatomical structure in the multicellular organism",
                    "Abnormality of thrombocytes",
                    "manual digit 1 phalanx",
                    "presumptive ectoderm",
                    "cranial nerve II phenotype",
                    "meso-epithelium",
                    "anucleate cell",
                    "Abnormal platelet morphology",
                    "platelet phenotype",
                    "ductus arteriosus",
                    "hindbrain morphology phenotype",
                    "circulatory system",
                    "system process phenotype",
                    "nervous system phenotype",
                    "cell layer",
                    "optic vesicle",
                    "serotonin secreting cell",
                    "metapodium bone 1 phenotype",
                    "pectoral complex",
                    "incomplete closing of the septum",
                    "decreased system process",
                    "decreased number of granulocyte",
                    "number of anatomical enitites of type mesoderm-derived structure phenotype",
                    "number of platelet phenotype",
                    "Thrombocytopenia",
                    "autopodial skeleton",
                    "ectoderm-derived structure atresia",
                    "decreased size of the bone element",
                    "decreased length of organism subdivision",
                    "biological_process rate phenotype",
                    "dorsal region element",
                    "digit morphology phenotype",
                    "decreased length of manual digit",
                    "decreased length of manual digit 1",
                    "absent bone of appendage girdle complex in the forelimb",
                    "absent endochondral element in the limb",
                    "segmental subdivision of hindbrain phenotype",
                    "manus phenotype",
                    "Short thumb",
                    "sensory perception of mechanical stimulus phenotype",
                    "macromolecule metabolic process phenotype",
                    "Abnormal digit morphology",
                    "Abnormal cardiovascular system morphology",
                    "neck phenotype",
                    "embryonic autopod plate",
                    "Abnormal hand morphology",
                    "decreased size of the manual digit",
                    "Gastrointestinal atresia",
                    "cerebellum phenotype",
                    "musculature phenotype",
                    "digit 1",
                    "bone marrow cell",
                    "decreased length of digit 1 or 5",
                    "cranial neuron projection bundle phenotype",
                    "closing of the subdivision of digestive tract",
                    "glandular system",
                    "paired limb/fin segment phenotype",
                    "transport phenotype",
                    "aplasia or hypoplasia of manual digit",
                    "absent skeletal element in the forelimb",
                    "absent limb endochondral element in the forelimb",
                    "biogenic amine secreting cell",
                    "Chiari malformation",
                    "lateral structure physiology phenotype",
                    "Fused cervical vertebrae",
                    "manual digit 1",
                    "segment of manus",
                    "ectoderm morphology phenotype",
                    "decreased length of manual digit 1 or 5",
                    "acropodium region",
                    "mesoderm",
                    "cardiogenic plate",
                    "neural tube",
                    "manual digitopodium region",
                    "manual digit 1 morphology phenotype",
                    "number of anatomical enitites of type skeletal element phenotype",
                    "mesoderm-derived structure phenotype",
                    "fused cervical vertebra and anatomical entity",
                    "commissure of telencephalon",
                    "decreased size of the autopodial extension",
                    "oxygen accumulating cell",
                    "articulation phenotype",
                    "decreased length of digit",
                    "decreased size of the bone of free limb or fin",
                    "retina",
                    "export from cell",
                    "Abnormality of the hand",
                    "manus",
                    "embryonic autopod plate morphology phenotype",
                    "manual digit plus metapodial segment",
                    "anatomical wall phenotype",
                    "cellular organisms",
                    "anatomical entity morphology in the manus phenotype",
                    "posterior segment of eyeball morphology phenotype",
                    "multi cell part structure",
                    "absent anatomical entity in the brain ventricle",
                    "central nervous system cell part cluster phenotype",
                    "head morphology phenotype",
                    "camera-type eye morphology phenotype",
                    "decreased length of material anatomical entity",
                    "neural plate morphology phenotype",
                    "Abnormality of skin pigmentation",
                    "Abnormal optic nerve morphology",
                    "number of anatomical enitites of type ectoderm-derived structure phenotype",
                    "decreased functionality of the endoderm-derived structure",
                    "curvature anatomical entity",
                    "Optic disc pallor",
                    "nervous system morphology phenotype",
                    "fused vertebra and anatomical entity",
                    "Eukaryota",
                    "forelimb skeleton",
                    "neuron projection bundle phenotype",
                    "subdivision of vertebral column phenotype",
                    "neuron projection bundle",
                    "central nervous system cell part cluster",
                    "photoreceptor array",
                    "decreased length of anatomical structure",
                    "Abnormality of chromosome stability",
                    "absent organism subdivision",
                    "Abnormal eye morphology",
                    "aplasia or hypoplasia of corpus callosum",
                    "chorioretinal region",
                    "Abnormality of the thyroid gland",
                    "fused anatomical entity and bony vertebral centrum",
                    "absent mesoderm-derived structure in the multicellular organism",
                    "organ component layer",
                    "decreased functionality of the endocrine gland",
                    "absent organ in the forelimb",
                    "autopodial extension phenotype",
                    "optic disc",
                    "organ subunit",
                    "metencephalon phenotype",
                    "Global developmental delay",
                    "Abnormal optic disc morphology",
                    "anterior neural tube phenotype",
                    "Metazoa",
                    "absent manual digit",
                    "central nervous system",
                    "Abnormal facial shape",
                    "absent endochondral element in the forelimb",
                    "retina phenotype",
                    "Abnormal circulating hormone concentration",
                    "trunk or cervical vertebra phenotype",
                    "brain ventricle phenotype",
                    "mesoderm morphology phenotype",
                    "musculature",
                    "craniocervical region morphology phenotype",
                    "number of anatomical enitites of type anatomical entity phenotype",
                    "absent anatomical structure",
                    "cranial nerve II morphology phenotype",
                    "multi cell part structure phenotype",
                    "lamina",
                    "nervous system process",
                    "Abnormal nervous system physiology",
                    "Abnormality of the eye",
                    "gastrula",
                    "Vesicoureteral reflux",
                    "multicellular organismal process phenotype",
                    "root",
                    "Eumetazoa",
                    "Growth delay",
                    "development of anatomical entity phenotype",
                    "decreased developmental process",
                    "ear morphology phenotype",
                    "Aplasia/hypoplasia involving the skeleton",
                    "thoracic cavity element phenotype",
                    "multicellular organism development",
                    "cranial nerve II",
                    "Intrauterine growth retardation",
                    "forelimb zeugopod bone hypoplasia",
                    "decreased anatomical structure development",
                    "Abnormality of the skin",
                    "subdivision of organism along appendicular axis phenotype",
                    "growth",
                    "sac",
                    "multi-limb segment region",
                    "developmental process",
                    "number of anatomical enitites of type anatomical structure phenotype",
                    "digit 1 phenotype",
                    "optic cup",
                    "embryo development phenotype",
                    "decreased multicellular organismal process",
                    "axon tract",
                    "acropodial skeleton",
                    "delayed biological_process",
                    "decreased biological_process",
                    "interatrial septum morphology phenotype",
                    "anatomical structure development phenotype",
                    "Thin corpus callosum",
                    "growth phenotype",
                    "developmental process rate phenotype",
                    "multicellular anatomical structure, asymmetrically curved phenotype",
                    "multicellular organismal process",
                    "closing of the organ part",
                    "hindbrain",
                    "decreased multicellular organism development",
                    "Decreased body weight",
                    "Abnormal size of pituitary gland",
                    "Aplasia/Hypoplasia of fingers",
                    "somite phenotype",
                    "gray matter of forebrain phenotype",
                    "Growth abnormality",
                    "absent septum pellucidum",
                    "ectoderm-derived structure physiology phenotype",
                    "decreased qualitatively anatomical structure development",
                    "biological_process phenotype",
                    "sensory perception of mechanical stimulus",
                    "decreased qualitatively sensory perception of sound",
                    "brain ventricle/choroid plexus morphology phenotype",
                    "bone of dorsum",
                    "phalanx morphology phenotype",
                    "decreased sensory perception of sound",
                    "multi organ part structure",
                    "signaling",
                    "vestibulo-auditory system",
                    "paraxial mesoderm phenotype",
                    "paired limb/fin skeleton",
                    "haemolymphatic fluid",
                    "vasculature of trunk phenotype",
                    "sensory perception of sound",
                    "fused vertebra and vertebra",
                    "ear physiology phenotype",
                    "incomplete closing of the interventricular septum",
                    "nervous system process phenotype",
                    "ventricle of nervous system",
                    "decreased nervous system process",
                    "vascular system",
                    "middle ear phenotype",
                    "vestibulo-auditory system phenotype",
                    "decreased sensory perception of mechanical stimulus",
                    "Finger aplasia",
                    "septum pellucidum phenotype",
                    "cardiac ventricle phenotype",
                    "absent digit",
                    "delayed growth",
                    "absent organism subdivision in the multicellular organism",
                    "Abnormal long bone morphology",
                    "aplastic manual digit 1",
                    "decreased size of the sense organ",
                    "negative regulation of biosynthetic process",
                    "Abnormality of globe size",
                    "Aplasia/hypoplasia of the extremities",
                    "gland phenotype",
                    "embryonic structure phenotype",
                    "endocrine gland phenotype",
                    "gland physiology phenotype",
                    "ocular fundus",
                    "endoderm-derived structure phenotype",
                    "decreased functionality of the anatomical structure",
                    "decreased functionality of the structure with developmental contribution from neural crest",
                    "thyroid gland physiology phenotype",
                    "Hypothyroidism",
                    "signal release",
                    "thyroid gland",
                    "white matter of telencephalon phenotype",
                    "closing of the subdivision of tube",
                    "Aplasia/hypoplasia involving bones of the hand",
                    "presomitic mesoderm morphology phenotype",
                    "endoderm-derived structure physiology phenotype",
                    "endocrine gland physiology phenotype",
                    "absent long bone in the forelimb",
                    "formed material anatomical entity",
                    "obsolete cell",
                    "brain phenotype",
                    "Abnormal axial skeleton morphology",
                    "sclerotome phenotype",
                    "decreased functionality of the anatomical entity",
                    "Abnormal eye physiology",
                    "decreased functionality of the gland",
                    "anatomical collection",
                    "fused skeletal joint and skeletal joint",
                    "anatomical entity height phenotype",
                    "decreased functionality of the organ",
                    "thyroid gland phenotype",
                    "anatomical collection phenotype",
                    "decreased functionality of the multicellular anatomical structure",
                    "endocrine system phenotype",
                    "radius bone phenotype",
                    "endocrine gland",
                    "multicellular organism development phenotype",
                    "brain",
                    "chordal neural plate",
                    "Abnormal hindbrain morphology",
                    "manual digit phenotype",
                    "anatomical entity morphology in the brain phenotype",
                    "Abnormal nervous system morphology",
                    "absent forelimb endochondral element in the limb",
                    "neural tube phenotype",
                    "Morphological central nervous system abnormality",
                    "cardiogenic splanchnic mesoderm morphology phenotype",
                    "Abnormal metencephalon morphology",
                    "Abnormal appendicular skeleton morphology",
                    "Abnormal atrial septum morphology",
                    "peptide transport",
                    "formed multicellular anatomical structure",
                    "Aplasia/Hypoplasia of the thumb",
                    "regional part of brain",
                    "segmental subdivision of nervous system",
                    "segmental subdivision of nervous system phenotype",
                    "formed regional part of nervous system",
                    "signal release phenotype",
                    "Hearing abnormality",
                    "absent bone of free limb or fin in the forelimb",
                    "Cerebellar malformation",
                    "regional part of nervous system",
                    "face morphology phenotype",
                    "Abnormal musculoskeletal physiology",
                    "eye primordium phenotype",
                    "aplasia or hypoplasia of manual digit 1",
                    "cerebellum",
                    "thoracic segment organ",
                    "segmental subdivision of hindbrain",
                    "Hypermelanotic macule",
                    "hindbrain phenotype",
                    "Abnormality of the nervous system",
                    "Vertebral segmentation defect",
                    "cell condensation phenotype",
                    "presomitic mesoderm",
                    "vertebral column phenotype",
                    "paraxial mesoderm",
                    "anatomical cluster",
                    "aplasia or hypoplasia of manual digit 1 phalanx",
                    "decreased qualitatively nervous system process",
                    "presumptive paraxial mesoderm phenotype",
                    "metapodium bone phenotype",
                    "Abnormal joint physiology",
                    "vasculature of organ",
                    "manual digit morphology in the manus phenotype",
                    "skeletal joint phenotype",
                    "epithelial vesicle",
                    "manual digit metacarpus endochondral element phenotype",
                    "incomplete closing of the multicellular anatomical structure",
                    "trunk mesenchyme",
                    "regulation of biosynthetic process",
                    "dorsal part of neck morphology phenotype",
                    "aplasia or hypoplasia of telencephalon",
                    "dorsal part of neck",
                    "neck bone",
                    "cervical region of vertebral column",
                    "optic vesicle phenotype",
                    "fused anatomical entity and cervical vertebra",
                    "Abnormal vertebral morphology",
                    "vertebral column morphology phenotype",
                    "Abnormal skin morphology",
                    "presomitic mesoderm phenotype",
                    "trunk or cervical vertebra",
                    "vertebral element phenotype",
                    "absent bone of pectoral complex in the forelimb",
                    "fused anatomical entity and anatomical entity",
                    "entire embryonic mesenchyme",
                    "platelet",
                    "irregular bone phenotype",
                    "musculoskeletal system physiology phenotype",
                    "peptide secretion phenotype",
                    "axial skeletal system",
                    "external acoustic meatus",
                    "vertebral column",
                    "subdivision of vertebral column",
                    "decreased length of digit 1",
                    "postcranial axial skeletal system",
                    "skeletal joint",
                    "axial skeleton plus cranial skeleton",
                    "absent endochondral bone",
                    "developing mesenchymal condensation",
                    "neck",
                    "telencephalon morphology phenotype",
                    "vertebra phenotype",
                    "fused anatomical entity and skeletal joint",
                    "primordium phenotype",
                    "fused vertebra and bony vertebral centrum",
                    "Aplasia/Hypoplasia of the optic nerve",
                    "hematopoietic cell",
                    "Optic nerve hypoplasia",
                    "decreased size of the endocrine gland",
                    "decreased length of neck",
                    "Aplasia/Hypoplasia affecting the fundus",
                    "cranial nerve II hypoplasia",
                    "organism substance",
                    "Abnormality of the endocrine system",
                    "hormone secretion",
                    "circulatory organ phenotype",
                    "peptide secretion",
                    "localization phenotype",
                    "decreased qualitatively system process",
                    "neck morphology phenotype",
                    "growth hormone secretion phenotype",
                    "trunk phenotype",
                    "biological regulation",
                    "Hypoplasia of the radius",
                    "nitrogen compound transport phenotype",
                    "Abnormal skeletal morphology",
                    "nitrogen compound transport",
                    "secretion",
                    "export from cell phenotype",
                    "decreased length of endochondral bone",
                    "structure with developmental contribution from neural crest physiology phenotype",
                    "cellular process phenotype",
                    "cellular process",
                    "posterior neural tube phenotype",
                    "growth hormone secretion",
                    "decreased qualitatively multicellular organism development",
                    "biological regulation phenotype",
                    "secretion by cell phenotype",
                    "bodily fluid",
                    "Abnormality of the neck",
                    "regulation of macromolecule biosynthetic process",
                    "Abnormality of the cervical spine",
                    "decreased number of leukocyte",
                    "postcranial axial skeleton phenotype",
                    "Abnormal neck morphology",
                    "nervous system physiology phenotype",
                    "Neurodevelopmental delay",
                    "decreased size of the forelimb long bone",
                    "Abnormal leukocyte morphology",
                    "negative regulation of metabolic process",
                    "number of anatomical enitites of type tissue phenotype",
                    "regulation of macromolecule metabolic process",
                    "Abnormality of metabolism/homeostasis",
                    "brain white matter phenotype",
                    "musculature of body phenotype",
                    "negative regulation of macromolecule metabolic process",
                    "biosynthetic process phenotype",
                ],
                "has_phenotype_count": 44,
                "score": None,
                "exact_synonyms": [
                    "FANCI|Fanconi Anemia, complementation group type 1|Fanconi anaemia complementation group type I|Fanconi anemia complementation group I|Fanconi anemia complementation group type I"
                ],
                "related_synonyms": ["Fanconi Anemia, complementation Group 1|Fanconi anemia, complementation group I"],
                "highlighting": None,
            },
            {
                "id": "MONDO:0011584",
                "category": "biolink:Disease",
                "name": "Fanconi anemia complementation group D1",
                "full_name": None,
                "deprecated": None,
                "description": "Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations is a rare cancer-predisposing syndrome, associated with the D1 subgroup of Fanconi anemia (FA), characterized by progressive bone marrow failure, cardiac, brain, intestinal or skeletal abnormalities and predisposition to various malignancies. Bone marrow suppression and the incidence of developmental abnormalities are less frequent than in other FA, but cancer risk is very high with the spectrum of childhood cancers including Wilms tumor, brain tumor (often medulloblastoma) and ALL/AML.",
                "xref": [
                    "DOID:0111089",
                    "GARD:17449",
                    "MEDGEN:325420",
                    "MESH:C563980",
                    "NCIT:C125705",
                    "OMIM:605724",
                    "Orphanet:319462",
                    "SCTID:766707003",
                    "UMLS:C1838457",
                ],
                "provided_by": "phenio_nodes",
                "in_taxon": None,
                "in_taxon_label": None,
                "symbol": None,
                "synonym": [
                    "FAD1",
                    "FANCD1",
                    "Fad1",
                    "Fanconi anemia complementation group D1",
                    "Fanconi anemia, complementation group D1",
                    "inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations",
                ],
                "broad_synonym": None,
                "exact_synonym": None,
                "narrow_synonym": None,
                "related_synonym": None,
                "subsets": ["clingen", "gard_rare", "nord_rare", "ordo_disorder", "orphanet_rare", "otar", "rare"],
                "uri": None,
                "iri": None,
                "namespace": "MONDO",
                "has_phenotype": [
                    "HP:0009778",
                    "HP:0005528",
                    "HP:0001511",
                    "HP:0004808",
                    "HP:0000957",
                    "HP:0003221",
                    "HP:0001508",
                    "HP:0004322",
                    "HP:0006727",
                    "HP:0002023",
                    "HP:0000252",
                ],
                "has_phenotype_label": [
                    "Short thumb",
                    "Bone marrow hypocellularity",
                    "Intrauterine growth retardation",
                    "Acute myeloid leukemia",
                    "Cafe-au-lait spot",
                    "Chromosomal breakage induced by crosslinking agents",
                    "Failure to thrive",
                    "Short stature",
                    "T-cell acute lymphoblastic leukemias",
                    "Anal atresia",
                    "Microcephaly",
                ],
                "has_phenotype_closure": [
                    "UBERON:0003914",
                    "UBERON:0013701",
                    "NCBITaxon:33208",
                    "UBERON:0000955",
                    "UBERON:0010371",
                    "UBERON:0001893",
                    "UPHENO:0087518",
                    "UPHENO:0087661",
                    "HP:0002060",
                    "UPHENO:0003177",
                    "UPHENO:0002553",
                    "UPHENO:0004615",
                    "UBERON:0016880",
                    "UPHENO:0076805",
                    "HP:0000252",
                    "NCBITaxon:6072",
                    "UPHENO:0004523",
                    "UPHENO:0075804",
                    "HP:0012443",
                    "NCBITaxon:33154",
                    "UPHENO:0005285",
                    "UBERON:0007811",
                    "UPHENO:0004621",
                    "HP:0012639",
                    "HP:0100547",
                    "UBERON:0003129",
                    "UBERON:0011137",
                    "HP:0000707",
                    "NCBITaxon:1",
                    "HP:0002011",
                    "UBERON:0016879",
                    "NCBITaxon:2759",
                    "UPHENO:0076702",
                    "UBERON:0000924",
                    "UPHENO:0002736",
                    "UBERON:0003056",
                    "UPHENO:0076799",
                    "UPHENO:0005030",
                    "UBERON:0000307",
                    "UPHENO:0086589",
                    "UPHENO:0002812",
                    "UPHENO:0003025",
                    "UPHENO:0002859",
                    "HP:0004378",
                    "UPHENO:0074237",
                    "UBERON:0004734",
                    "UPHENO:0074229",
                    "UBERON:0002346",
                    "HP:0002023",
                    "UPHENO:0063599",
                    "UPHENO:0063581",
                    "HP:0040195",
                    "UBERON:0000025",
                    "UPHENO:0063596",
                    "HP:0025033",
                    "HP:0025031",
                    "UPHENO:0004484",
                    "UBERON:0004111",
                    "UBERON:0001890",
                    "UBERON:0001555",
                    "HP:0000929",
                    "HP:0006721",
                    "UPHENO:0081423",
                    "HP:0004322",
                    "UPHENO:0080352",
                    "UPHENO:0080351",
                    "UPHENO:0010795",
                    "UPHENO:0075159",
                    "UPHENO:0082761",
                    "UPHENO:0010850",
                    "UPHENO:0005431",
                    "HP:0001508",
                    "UBERON:0000481",
                    "HP:0007364",
                    "UPHENO:0004521",
                    "UPHENO:0010799",
                    "HP:0025354",
                    "GO:0060255",
                    "UBERON:0002616",
                    "GO:0009889",
                    "GO:0010467",
                    "GO:0050789",
                    "GO:0010468",
                    "GO:0010558",
                    "GO:0050794",
                    "GO:0043170",
                    "UPHENO:0049873",
                    "GO:0008152",
                    "HP:0001939",
                    "GO:0009890",
                    "UPHENO:0063577",
                    "UPHENO:0050007",
                    "GO:0031049",
                    "GO:0010629",
                    "GO:0019222",
                    "UPHENO:0054315",
                    "GO:0048523",
                    "UBERON:0001245",
                    "UPHENO:0081424",
                    "HP:0040012",
                    "UPHENO:0049837",
                    "UPHENO:0049835",
                    "GO:0043473",
                    "HP:0000951",
                    "UPHENO:0002548",
                    "UPHENO:0002839",
                    "UPHENO:0003811",
                    "HP:0006727",
                    "UBERON:0002097",
                    "HP:0001000",
                    "HP:0004325",
                    "UPHENO:0080662",
                    "UPHENO:0054957",
                    "UBERON:0010323",
                    "UBERON:0002416",
                    "HP:0001574",
                    "HP:0001034",
                    "HP:0000953",
                    "CL:0002191",
                    "HP:0002664",
                    "CL:0011026",
                    "CL:0000738",
                    "HP:0004808",
                    "HP:0032251",
                    "HP:0010987",
                    "UPHENO:0050065",
                    "GO:0065007",
                    "HP:0002488",
                    "CL:0000988",
                    "CL:0000219",
                    "NCBITaxon:131567",
                    "UBERON:0002090",
                    "UPHENO:0074575",
                    "CL:0000763",
                    "UPHENO:0086172",
                    "UPHENO:0087123",
                    "UPHENO:3000003",
                    "HP:0002715",
                    "UPHENO:0003186",
                    "CL:0000835",
                    "CL:0000839",
                    "UPHENO:0088166",
                    "UBERON:0001049",
                    "HP:0011793",
                    "UPHENO:0005573",
                    "UPHENO:0005647",
                    "UPHENO:0081436",
                    "HP:0012733",
                    "UPHENO:0050108",
                    "UPHENO:0075220",
                    "GO:0048856",
                    "UPHENO:0003004",
                    "UPHENO:0005597",
                    "CL:0002031",
                    "UPHENO:0052160",
                    "UPHENO:0080377",
                    "HP:0001507",
                    "UBERON:0011676",
                    "GO:0009790",
                    "UPHENO:0050068",
                    "UPHENO:0080393",
                    "HP:0001510",
                    "UPHENO:0054374",
                    "BFO:0000015",
                    "GO:0040007",
                    "UBERON:0011138",
                    "UPHENO:0080382",
                    "UPHENO:0086679",
                    "UPHENO:0052178",
                    "GO:0048519",
                    "UPHENO:0050106",
                    "UPHENO:0003001",
                    "UPHENO:0049587",
                    "UPHENO:0080200",
                    "BFO:0000003",
                    "UPHENO:0000541",
                    "UPHENO:0049874",
                    "UBERON:0010000",
                    "UPHENO:0003236",
                    "UBERON:0000075",
                    "UPHENO:0049870",
                    "HP:0002817",
                    "UPHENO:0081566",
                    "UPHENO:0002564",
                    "UBERON:0004765",
                    "UPHENO:0087663",
                    "UPHENO:3000000",
                    "UPHENO:0002530",
                    "UPHENO:0074228",
                    "UPHENO:0003812",
                    "UPHENO:0076791",
                    "UBERON:0019221",
                    "HP:0033127",
                    "HP:0000234",
                    "UBERON:0015061",
                    "UPHENO:0004802",
                    "UPHENO:0002632",
                    "HP:0001909",
                    "HP:0001881",
                    "UBERON:0004347",
                    "UPHENO:0002905",
                    "UBERON:0005419",
                    "GO:0009892",
                    "HP:0005561",
                    "HP:0000002",
                    "UPHENO:0000543",
                    "UPHENO:0002949",
                    "UBERON:0010316",
                    "GO:0042592",
                    "HP:0000924",
                    "UPHENO:0046505",
                    "UBERON:0001016",
                    "HP:0004323",
                    "UPHENO:0001001",
                    "HP:0007400",
                    "UBERON:0010708",
                    "UBERON:0000073",
                    "UBERON:0000161",
                    "UBERON:0002405",
                    "UBERON:0005944",
                    "HP:0000957",
                    "UBERON:0005423",
                    "UPHENO:0046552",
                    "UBERON:0001017",
                    "UPHENO:0074230",
                    "UPHENO:0002568",
                    "UPHENO:0002945",
                    "UBERON:0001440",
                    "UPHENO:0002764",
                    "UBERON:0000061",
                    "UPHENO:0002708",
                    "HP:0009381",
                    "UPHENO:0004909",
                    "HP:0009815",
                    "UPHENO:0076703",
                    "UPHENO:0080114",
                    "UPHENO:0002926",
                    "HP:0005922",
                    "UPHENO:0003159",
                    "UPHENO:0087006",
                    "UPHENO:0046426",
                    "UBERON:0000475",
                    "UBERON:0007524",
                    "UPHENO:0003163",
                    "UPHENO:0002747",
                    "UBERON:0006598",
                    "UBERON:0005417",
                    "HP:0004377",
                    "BFO:0000002",
                    "UPHENO:0002554",
                    "UPHENO:0053456",
                    "UBERON:0008785",
                    "UPHENO:0076727",
                    "GO:0009058",
                    "UBERON:0010130",
                    "UPHENO:0050121",
                    "UPHENO:0002593",
                    "UBERON:0011249",
                    "UPHENO:0002731",
                    "UPHENO:0046624",
                    "UPHENO:0005642",
                    "HP:0001167",
                    "UPHENO:0004064",
                    "UBERON:0010758",
                    "UPHENO:0046528",
                    "UBERON:0003075",
                    "UPHENO:0003095",
                    "HP:0040064",
                    "HP:0002977",
                    "UPHENO:0080099",
                    "UBERON:0002193",
                    "UBERON:0001062",
                    "UPHENO:0088123",
                    "CL:0000255",
                    "UPHENO:0004466",
                    "UPHENO:0069327",
                    "UBERON:0002101",
                    "UPHENO:0002586",
                    "UPHENO:0002526",
                    "UPHENO:0069254",
                    "UBERON:0002470",
                    "UBERON:0000923",
                    "UBERON:0004708",
                    "BFO:0000004",
                    "UBERON:0004121",
                    "UBERON:0000062",
                    "UBERON:0003081",
                    "UBERON:0034923",
                    "UPHENO:0002782",
                    "HP:0009121",
                    "UBERON:5001463",
                    "UBERON:0001007",
                    "UBERON:0002544",
                    "CL:0008001",
                    "UBERON:0010740",
                    "CL:0011115",
                    "UPHENO:0003005",
                    "UPHENO:0086546",
                    "HP:0011927",
                    "UPHENO:0003049",
                    "UPHENO:0087660",
                    "UPHENO:0012312",
                    "UPHENO:0076724",
                    "UPHENO:0004892",
                    "UPHENO:0086633",
                    "UBERON:0006601",
                    "UPHENO:0002833",
                    "UBERON:0003102",
                    "UPHENO:0001002",
                    "HP:0009601",
                    "UBERON:0000483",
                    "UBERON:0002050",
                    "HP:0001511",
                    "UPHENO:0088186",
                    "UPHENO:0084761",
                    "HP:0011121",
                    "UBERON:0000468",
                    "UPHENO:0054304",
                    "UPHENO:0075195",
                    "HP:0000118",
                    "UBERON:0004710",
                    "UBERON:0000922",
                    "UBERON:0011582",
                    "UPHENO:0054970",
                    "GO:0007275",
                    "UPHENO:0069605",
                    "UBERON:0003104",
                    "UPHENO:0079876",
                    "UPHENO:0004519",
                    "UPHENO:0002870",
                    "UPHENO:0002559",
                    "UPHENO:0002536",
                    "HP:0011017",
                    "UPHENO:0086769",
                    "HP:0009778",
                    "UPHENO:0005214",
                    "HP:0012145",
                    "UPHENO:0052694",
                    "UBERON:0000153",
                    "HP:0011842",
                    "UPHENO:0046707",
                    "GO:0005623",
                    "UPHENO:0076692",
                    "UPHENO:0003366",
                    "UBERON:0010538",
                    "UBERON:0001463",
                    "UBERON:5002389",
                    "UBERON:0003080",
                    "UPHENO:0002944",
                    "UPHENO:0076697",
                    "UPHENO:0002541",
                    "UBERON:0004288",
                    "HP:0011297",
                    "UPHENO:0002880",
                    "UBERON:0002102",
                    "UBERON:0002428",
                    "UPHENO:0074245",
                    "UPHENO:0002733",
                    "UPHENO:0076803",
                    "UBERON:0002529",
                    "UPHENO:0068971",
                    "UPHENO:0002830",
                    "UPHENO:0002983",
                    "UBERON:0000465",
                    "UPHENO:0087907",
                    "UPHENO:0003799",
                    "UBERON:0006717",
                    "HP:0045060",
                    "UPHENO:0086700",
                    "UPHENO:0050008",
                    "GO:0032502",
                    "UBERON:0012139",
                    "UPHENO:0002746",
                    "HP:0000240",
                    "UPHENO:0053208",
                    "UPHENO:0078606",
                    "UPHENO:0002577",
                    "UPHENO:0002648",
                    "UBERON:0004375",
                    "UPHENO:0081581",
                    "UPHENO:0080126",
                    "UPHENO:0003334",
                    "UPHENO:0002976",
                    "UPHENO:0069266",
                    "UPHENO:0003069",
                    "UBERON:0000033",
                    "GO:0010605",
                    "UBERON:0000926",
                    "UPHENO:0086635",
                    "UPHENO:0046411",
                    "UBERON:0002389",
                    "RO:0002577",
                    "UPHENO:0046483",
                    "HP:0006496",
                    "UBERON:0012475",
                    "UBERON:0010912",
                    "UPHENO:0063594",
                    "HP:0009115",
                    "UPHENO:0086644",
                    "BFO:0000040",
                    "UPHENO:0086485",
                    "UPHENO:0005596",
                    "UPHENO:0004476",
                    "HP:0000152",
                    "UPHENO:0002896",
                    "UPHENO:0002635",
                    "UBERON:0004381",
                    "CL:0000000",
                    "UBERON:0007272",
                    "UPHENO:0004900",
                    "UPHENO:0002567",
                    "HP:0003221",
                    "UBERON:0010707",
                    "UBERON:0010712",
                    "UPHENO:0005055",
                    "UPHENO:0012440",
                    "UPHENO:0002650",
                    "UPHENO:0005433",
                    "UPHENO:0069236",
                    "GO:0008150",
                    "HP:0040068",
                    "UPHENO:0046445",
                    "UPHENO:0052778",
                    "UPHENO:0002542",
                    "UPHENO:0046741",
                    "UPHENO:0063565",
                    "UPHENO:0069062",
                    "UBERON:0002204",
                    "UPHENO:0074584",
                    "UBERON:0005451",
                    "UBERON:0002398",
                    "UBERON:0012354",
                    "HP:0005528",
                    "UPHENO:0002861",
                    "CL:0001035",
                    "UPHENO:0084448",
                    "UBERON:0005291",
                    "UPHENO:0002571",
                    "GO:0010556",
                    "UPHENO:0002600",
                    "UPHENO:0049904",
                    "UPHENO:0002964",
                    "UPHENO:0005141",
                    "UPHENO:0010763",
                    "UBERON:0034925",
                    "UPHENO:0005092",
                    "UPHENO:0004704",
                    "UBERON:0015212",
                    "UPHENO:0004888",
                    "HP:0001155",
                    "UBERON:0001015",
                    "UPHENO:0002844",
                    "UBERON:0001434",
                    "UBERON:0004120",
                    "UBERON:0000383",
                    "UBERON:0011216",
                    "UBERON:0002390",
                    "UPHENO:0049652",
                    "UPHENO:0069684",
                    "UPHENO:0002948",
                    "UPHENO:0084763",
                    "UPHENO:0046740",
                    "HP:0003220",
                    "UPHENO:0076740",
                    "UPHENO:0003415",
                    "UPHENO:0069674",
                    "UBERON:5006048",
                    "GO:0009059",
                    "UBERON:0001474",
                    "UPHENO:0074227",
                    "HP:0011844",
                    "UBERON:0015203",
                    "UPHENO:0010808",
                    "GO:0032501",
                    "UBERON:0006048",
                    "UPHENO:0002902",
                    "UBERON:0001442",
                    "HP:0005927",
                    "UPHENO:0003227",
                    "UPHENO:0004885",
                    "UBERON:0019231",
                    "HP:0000001",
                    "UPHENO:0087347",
                    "UBERON:0012140",
                    "UPHENO:0080079",
                    "UPHENO:0012274",
                    "UPHENO:0004475",
                    "UPHENO:0053330",
                    "BFO:0000001",
                    "UPHENO:0063558",
                    "UPHENO:0076723",
                    "CL:0002242",
                    "UPHENO:0002963",
                    "UPHENO:0003065",
                    "UBERON:0006058",
                    "HP:0002813",
                    "UPHENO:0002816",
                    "UPHENO:0003514",
                    "UBERON:0002199",
                    "UPHENO:0002525",
                    "UPHENO:0003432",
                    "UPHENO:0087665",
                    "UBERON:0000467",
                    "UBERON:0002513",
                    "UPHENO:0046750",
                    "UPHENO:0063562",
                    "UPHENO:0050034",
                    "HP:0001172",
                    "UBERON:0013702",
                    "UPHENO:0004680",
                    "UPHENO:0087363",
                    "UPHENO:0087849",
                    "HP:0006265",
                    "UPHENO:0012308",
                    "UPHENO:0076739",
                    "UBERON:0002091",
                    "UPHENO:0003082",
                    "UBERON:0004357",
                    "UBERON:0000479",
                    "HP:0011355",
                    "UBERON:0000026",
                    "UBERON:5002544",
                    "UBERON:0001460",
                    "UPHENO:0004459",
                    "HP:0034915",
                    "UBERON:0010363",
                    "UBERON:0005881",
                    "UBERON:0010314",
                    "UPHENO:0082794",
                    "UBERON:0012141",
                    "UPHENO:0001003",
                    "UBERON:0002371",
                    "GO:0031052",
                    "CL:0002092",
                    "UPHENO:0002668",
                    "HP:0001871",
                    "GO:0009987",
                    "UPHENO:0049966",
                ],
                "has_phenotype_closure_label": [
                    "Decreased head circumference",
                    "gastrula",
                    "nervous system phenotype",
                    "multi-tissue structure phenotype",
                    "epithelium",
                    "neural tube",
                    "future central nervous system phenotype",
                    "head phenotype",
                    "axial skeleton plus cranial skeleton",
                    "cranial skeletal system",
                    "skull",
                    "craniocervical region phenotype",
                    "Metazoa",
                    "epithelium phenotype",
                    "regional part of nervous system",
                    "central nervous system phenotype",
                    "regional part of brain",
                    "forebrain morphology phenotype",
                    "body proper",
                    "ecto-epithelium",
                    "presumptive ectoderm phenotype",
                    "neurectoderm",
                    "Abnormal cerebral morphology",
                    "ectoderm",
                    "neural plate morphology phenotype",
                    "craniofacial/craniocervical phenotype",
                    "future nervous system",
                    "brain phenotype",
                    "Abnormal axial skeleton morphology",
                    "epithelial tube",
                    "main body axis",
                    "Abnormality of head or neck",
                    "nervous system",
                    "Abnormal nervous system morphology",
                    "anterior neural tube phenotype",
                    "regional part of nervous system phenotype",
                    "closing of the ectoderm-derived structure",
                    "closing of the material anatomical entity",
                    "anus morphology phenotype",
                    "Eukaryota",
                    "anus",
                    "digestive system morphology phenotype",
                    "Aplasia/Hypoplasia involving the central nervous system",
                    "orifice",
                    "Abnormality of the digestive system",
                    "tube",
                    "digestive system phenotype",
                    "tube phenotype",
                    "telencephalon morphology phenotype",
                    "anus phenotype",
                    "closing of the anatomical entity",
                    "forebrain phenotype",
                    "closing of the anatomical structure",
                    "closing of the multicellular anatomical structure",
                    "size of multicellular organism phenotype",
                    "decreased size of the multicellular organism",
                    "decreased height of the multicellular organism",
                    "multicellular organism height phenotype",
                    "decreased height of the anatomical entity",
                    "Decreased multicellular organism mass",
                    "multicellular anatomical structure mass phenotype",
                    "decreased material anatomical entity mass",
                    "multicellular organism mass phenotype",
                    "subdivision of organism along main body axis phenotype",
                    "Decreased anatomical entity mass",
                    "material anatomical entity mass phenotype",
                    "Decreased body weight",
                    "neural plate phenotype",
                    "decreased anatomical structure mass",
                    "obsolete cell",
                    "Abnormal brain morphology",
                    "Chromosomal breakage induced by crosslinking agents",
                    "regional part of brain phenotype",
                    "regulation of gene expression",
                    "negative regulation of macromolecule biosynthetic process",
                    "cellular process",
                    "Abnormal cellular phenotype",
                    "skull phenotype",
                    "Failure to thrive",
                    "gene expression phenotype",
                    "postcranial axial skeleton",
                    "anatomical conduit",
                    "metabolic process phenotype",
                    "regulation of metabolic process",
                    "macromolecule biosynthetic process",
                    "biological regulation phenotype",
                    "programmed DNA elimination",
                    "negative regulation of gene expression",
                    "regulation of cellular process",
                    "negative regulation of biological process",
                    "Chromosome breakage",
                    "negative regulation of macromolecule metabolic process",
                    "metabolic process",
                    "Abnormality of the head",
                    "Abnormality of metabolism/homeostasis",
                    "regulation of macromolecule metabolic process",
                    "regulation of biosynthetic process",
                    "negative regulation of metabolic process",
                    "pigmentation phenotype",
                    "integument phenotype",
                    "integumental system",
                    "Hyperpigmentation of the skin",
                    "skin of body",
                    "aplasia or hypoplasia of telencephalon",
                    "integument",
                    "brain morphology phenotype",
                    "programmed DNA elimination by chromosome breakage",
                    "increased pigmentation in skin of body",
                    "Irregular hyperpigmentation",
                    "Abnormality of skin pigmentation",
                    "increased qualitatively biological_process",
                    "increased pigmentation",
                    "skin of body phenotype",
                    "blastula",
                    "increased biological_process",
                    "skin of body morphology phenotype",
                    "Localized skin lesion",
                    "future central nervous system",
                    "leukocyte morphology phenotype",
                    "cell phenotype",
                    "multi-tissue structure",
                    "progenitor cell",
                    "leukocyte",
                    "neoplasm phenotype",
                    "Abnormal skull morphology",
                    "myeloblast",
                    "myeloid lineage restricted progenitor cell",
                    "Acute leukemia",
                    "Abnormality of the anus",
                    "Neoplasm",
                    "homeostatic process phenotype",
                    "Abnormal leukocyte morphology",
                    "Anal atresia",
                    "hematopoietic precursor cell",
                    "myeloid cell",
                    "immune system morphology phenotype",
                    "Leukemia",
                    "hematopoietic cell",
                    "Opisthokonta",
                    "anatomical entity mass phenotype",
                    "motile cell",
                    "Short stature",
                    "nucleate cell",
                    "head morphology phenotype",
                    "ectoderm-derived structure",
                    "biological_process phenotype",
                    "Intrauterine growth retardation",
                    "decreased qualitatively anatomical structure development",
                    "anterior neural tube",
                    "biological_process",
                    "pre-chordal neural plate phenotype",
                    "digestive tract",
                    "granulocytopoietic cell",
                    "delayed growth",
                    "ectoderm morphology phenotype",
                    "developmental process rate phenotype",
                    "Abnormal forebrain morphology",
                    "decreased qualitatively embryo development",
                    "anatomical structure development phenotype",
                    "neural tube morphology phenotype",
                    "embryo development rate phenotype",
                    "decreased qualitatively multicellular organismal process",
                    "delayed biological_process",
                    "decreased qualitatively developmental process",
                    "embryo development phenotype",
                    "decreased embryo development",
                    "decreased qualitatively multicellular organism development",
                    "Abnormal immune system morphology",
                    "decreased qualitatively biological_process",
                    "decreased anatomical structure development",
                    "multicellular organism development",
                    "decreased developmental process",
                    "multicellular organismal process phenotype",
                    "anatomical structure development",
                    "developmental process phenotype",
                    "germ layer",
                    "Aplasia/Hypoplasia of the cerebrum",
                    "embryo development",
                    "multicellular organism morphology phenotype",
                    "Abnormal cellular immune system morphology",
                    "continuant",
                    "limb",
                    "disconnected anatomical group",
                    "manual digit morphology in the manus phenotype",
                    "structure with developmental contribution from neural crest phenotype",
                    "mesoderm morphology phenotype",
                    "decreased size of the manual digit",
                    "Short finger",
                    "digitopodium region",
                    "lateral plate mesoderm phenotype",
                    "autopodial skeleton",
                    "subdivision of skeleton",
                    "Morphological central nervous system abnormality",
                    "decreased length of manual digit 1",
                    "neurectoderm phenotype",
                    "appendage",
                    "Abnormal digit morphology",
                    "limb bud phenotype",
                    "Aplasia/Hypoplasia of fingers",
                    "paired limb/fin skeleton",
                    "pectoral appendage bud phenotype",
                    "phenotypic effect",
                    "developing anatomical structure",
                    "Abnormal digestive system morphology",
                    "decreased length of anatomical structure",
                    "Abnormal appendicular skeleton morphology",
                    "Abnormality of the nervous system",
                    "multicellular anatomical structure",
                    "limb morphology phenotype",
                    "decreased size of the anatomical entity",
                    "lateral structure phenotype",
                    "developing anatomical structure phenotype",
                    "pre-chordal neural plate",
                    "musculature",
                    "arm",
                    "negative regulation of biosynthetic process",
                    "germ layer / neural crest phenotype",
                    "size of skull phenotype",
                    "anatomical collection",
                    "precursor cell",
                    "manus",
                    "mesoderm-derived structure phenotype",
                    "bone of appendage girdle complex",
                    "embryonic autopod plate",
                    "independent continuant",
                    "digit 1 or 5",
                    "Aplasia/hypoplasia involving bones of the extremities",
                    "tissue phenotype",
                    "manual digit",
                    "biological regulation",
                    "pectoral complex",
                    "decreased length of autopodial extension",
                    "decreased multicellular organismal process",
                    "digit",
                    "manual digit 1 plus metapodial segment",
                    "endochondral element",
                    "anatomical entity height phenotype",
                    "organism subdivision",
                    "germ layer / neural crest",
                    "Abnormal hand morphology",
                    "anatomical system",
                    "Aplasia/hypoplasia involving the skeleton",
                    "aplasia or hypoplasia of manual digit 1",
                    "appendicular skeleton",
                    "regulation of macromolecule biosynthetic process",
                    "appendage girdle complex",
                    "anus atresia",
                    "material entity",
                    "decreased multicellular anatomical structure mass",
                    "tissue",
                    "craniocervical region",
                    "manual digit 1",
                    "Aplasia/hypoplasia involving bones of the upper limbs",
                    "appendicular skeleton phenotype",
                    "mesoderm",
                    "limb segment phenotype",
                    "Aplasia/hypoplasia involving bones of the hand",
                    "decreased length of anatomical entity",
                    "anatomical structure atresia",
                    "anatomical entity morphology in the pectoral complex phenotype",
                    "gene expression",
                    "Abnormality of the upper limb",
                    "embryo",
                    "Short digit",
                    "decreased multicellular organism development",
                    "manual digitopodium region",
                    "ecto-epithelium phenotype",
                    "decreased biological_process",
                    "phenotype",
                    "digit 1 plus metapodial segment",
                    "gastrula morphology phenotype",
                    "decreased qualitatively growth",
                    "Cafe-au-lait spot",
                    "decreased size of the multicellular anatomical structure in the pectoral complex",
                    "autopodial extension phenotype",
                    "limb skeleton subdivision phenotype",
                    "forelimb bud",
                    "bone element",
                    "presumptive structure phenotype",
                    "skeleton",
                    "paired limb/fin phenotype",
                    "Abnormality of the musculoskeletal system",
                    "decreased length of manual digit 1 or 5",
                    "regulation of biological process",
                    "skeletal element phenotype",
                    "paired limb/fin segment",
                    "digit 1 phenotype",
                    "Abnormal finger morphology",
                    "neural plate",
                    "Abnormality of body height",
                    "limb endochondral element",
                    "paired limb/fin bud",
                    "bone of appendage girdle complex phenotype",
                    "subdivision of organism along main body axis",
                    "Abnormality of the skin",
                    "development of anatomical entity phenotype",
                    "decreased size of the anatomical structure in the pectoral complex",
                    "Eumetazoa",
                    "immune system phenotype",
                    "digit 1 or 5 phenotype",
                    "paired limb/fin",
                    "telencephalon phenotype",
                    "negative regulation of gene expression phenotype",
                    "decreased length of material anatomical entity",
                    "skull morphology phenotype",
                    "paired limb/fin skeleton phenotype",
                    "bone of free limb or fin phenotype",
                    "aplasia or hypoplasia of manual digit",
                    "Acute myeloid leukemia",
                    "paired limb/fin segment phenotype",
                    "programmed DNA elimination by chromosome breakage phenotype",
                    "skeleton of limb",
                    "paired limb/fin bud phenotype",
                    "root",
                    "skeleton of manus",
                    "upper limb segment phenotype",
                    "eukaryotic cell",
                    "endochondral bone",
                    "forelimb bud phenotype",
                    "multicellular anatomical structure phenotype",
                    "decreased size of the multicellular anatomical structure",
                    "mesoderm-derived structure",
                    "lateral structure",
                    "Hematological neoplasm",
                    "Short thumb",
                    "lateral plate mesoderm",
                    "pectoral appendage skeleton",
                    "Abnormality of multiple cell lineages in the bone marrow",
                    "multicellular organismal process",
                    "digit plus metapodial segment",
                    "aplasia or hypoplasia of skeleton",
                    "craniocervical region morphology phenotype",
                    "integumental system phenotype",
                    "skeletal system",
                    "central nervous system",
                    "pigmentation",
                    "organ phenotype",
                    "negative regulation of cellular process",
                    "musculature phenotype",
                    "immune system",
                    "forelimb bud morphology phenotype",
                    "brain",
                    "mesenchyme",
                    "non-connected functional system",
                    "Abnormal thumb morphology",
                    "digit morphology phenotype",
                    "endochondral bone phenotype",
                    "Hypermelanotic macule",
                    "anatomical entity morphology phenotype",
                    "anatomical entity atresia",
                    "biosynthetic process phenotype",
                    "pectoral appendage",
                    "multicellular organism development phenotype",
                    "anatomical system phenotype",
                    "multi-limb segment region",
                    "decreased growth",
                    "organ",
                    "skeletal element",
                    "telencephalon",
                    "macromolecule metabolic process phenotype",
                    "limb endochondral element phenotype",
                    "Abnormal anus morphology",
                    "forelimb skeleton",
                    "decreased size of the anatomical structure",
                    "orifice atresia",
                    "taxon specific phenotype",
                    "hematopoietic lineage restricted progenitor cell",
                    "musculoskeletal system phenotype",
                    "aplasia or hypoplasia of anatomical entity",
                    "organ system subdivision",
                    "Microcephaly",
                    "embryo phenotype",
                    "decreased length of organism subdivision",
                    "increased biological_process in skin of body",
                    "segment of autopod",
                    "Abnormal skin morphology",
                    "appendicular skeletal system",
                    "digit phenotype",
                    "forebrain",
                    "Abnormality of limb bone",
                    "limb segment",
                    "autopodial extension",
                    "decreased length of multicellular anatomical structure",
                    "Aplasia/Hypoplasia of the thumb",
                    "Abnormal cellular physiology",
                    "cell",
                    "decreased size of the material anatomical entity",
                    "size of anatomical entity phenotype",
                    "anatomical entity",
                    "manus phenotype",
                    "surface structure",
                    "embryo morphology phenotype",
                    "decreased size of the organism subdivision",
                    "germ layer phenotype",
                    "multi-limb segment region phenotype",
                    "embryonic structure phenotype",
                    "cranial skeletal system phenotype",
                    "closing of the anatomical conduit",
                    "cellular process phenotype",
                    "pectoral appendage bud",
                    "forelimb morphology phenotype",
                    "anatomical structure phenotype",
                    "endochondral element phenotype",
                    "Abnormal skeletal morphology",
                    "skeletal system morphology phenotype",
                    "anterior region of body",
                    "Acute lymphoblastic leukemia",
                    "Abnormality of the integument",
                    "system",
                    "appendage phenotype",
                    "limb phenotype",
                    "embryonic structure",
                    "skeletal system phenotype",
                    "arm phenotype",
                    "forelimb phenotype",
                    "anatomical structure mass phenotype",
                    "process",
                    "skeleton phenotype",
                    "axial skeletal system",
                    "nervous system morphology phenotype",
                    "multicellular organism",
                    "manual digit 1 or 5",
                    "material anatomical entity atresia",
                    "musculature of body phenotype",
                    "digit 1",
                    "mesenchyme morphology phenotype",
                    "skeleton of limb phenotype",
                    "bone of free limb or fin",
                    "limb bone",
                    "Abnormality of body weight",
                    "upper limb segment",
                    "central nervous system morphology phenotype",
                    "structure with developmental contribution from neural crest",
                    "manual digit 1 morphology phenotype",
                    "ectoderm-derived structure phenotype",
                    "anatomical entity length phenotype",
                    "Abnormal bone marrow cell morphology",
                    "embryonic tissue phenotype",
                    "growth phenotype",
                    "subdivision of skeletal system phenotype",
                    "ectoderm-derived structure atresia",
                    "occurrent",
                    "manual digit plus metapodial segment",
                    "hemolymphoid system",
                    "Abnormality of chromosome stability",
                    "germ layer morphology phenotype",
                    "mesenchyme phenotype",
                    "Abnormality of skull size",
                    "presumptive ectoderm",
                    "dense mesenchyme tissue phenotype",
                    "subdivision of skeleton phenotype",
                    "dense mesenchyme tissue",
                    "presumptive structure",
                    "anatomical entity phenotype",
                    "subdivision of skeletal system",
                    "Abnormality of the immune system",
                    "decreased size of the digit",
                    "cellular organisms",
                    "macromolecule metabolic process",
                    "developmental process",
                    "forelimb",
                    "anatomical collection phenotype",
                    "decreased size of the autopodial extension",
                    "biological_process rate phenotype",
                    "subdivision of organism along appendicular axis phenotype",
                    "homeostatic process",
                    "organism subdivision phenotype",
                    "epithelial tube phenotype",
                    "musculoskeletal system",
                    "decreased size of the anatomical entity in the pectoral complex",
                    "Neoplasm by anatomical site",
                    "decreased length of digit 1 or 5",
                    "Abnormal limb bone morphology",
                    "macromolecule biosynthetic process phenotype",
                    "biosynthetic process",
                    "limb bone phenotype",
                    "skeleton of pectoral complex",
                    "limb bone morphology phenotype",
                    "growth",
                    "manual digit phenotype",
                    "entity",
                    "segment of manus",
                    "Abnormality of the skeletal system",
                    "manus morphology phenotype",
                    "hematopoietic system phenotype",
                    "acropodium region",
                    "autopod region phenotype",
                    "digestive system",
                    "bone cell",
                    "All",
                    "subdivision of organism along appendicular axis",
                    "mesoderm phenotype",
                    "anatomical structure",
                    "head",
                    "neural tube phenotype",
                    "organ system subdivision phenotype",
                    "Bone marrow hypocellularity",
                    "musculature of body",
                    "Phenotypic abnormality",
                    "hematopoietic system",
                    "limb skeleton subdivision",
                    "anatomical entity morphology in the manus phenotype",
                    "surface structure phenotype",
                    "Macule",
                    "bone element phenotype",
                    "orifice phenotype",
                    "embryonic tissue morphology phenotype",
                    "Growth abnormality",
                    "multicellular organism phenotype",
                    "limb bud",
                    "postcranial axial skeletal system",
                    "multicellular anatomical structure atresia",
                    "embryonic autopod plate morphology phenotype",
                    "appendicular skeleton morphology phenotype",
                    "anatomical entity morphology in the appendage girdle complex phenotype",
                    "decreased length of digit",
                    "decreased length of manual digit",
                    "embryonic tissue",
                    "T-cell acute lymphoblastic leukemias",
                    "Aplasia/hypoplasia of the extremities",
                    "decreased size of the material anatomical entity in the pectoral complex",
                    "Growth delay",
                    "Abnormality of the hand",
                    "ectoderm phenotype",
                    "pectoral appendage phenotype",
                    "material anatomical entity phenotype",
                    "decreased length of digit 1",
                    "autopod region",
                    "material anatomical entity",
                    "limb bud morphology phenotype",
                    "anatomical conduit phenotype",
                    "Abnormality of limbs",
                    "autopod region morphology phenotype",
                    "lateral plate mesoderm morphology phenotype",
                    "Abnormality of blood and blood-forming tissues",
                    "anatomical conduit atresia",
                    "bone marrow cell",
                    "bone marrow",
                ],
                "has_phenotype_count": 11,
                "score": None,
                "exact_synonyms": ["FAD1|FANCD1|Fanconi anemia complementation group D1"],
                "related_synonyms": [
                    "Fad1|Fanconi anemia, complementation group D1|inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations"
                ],
                "highlighting": None,
            },
        ],
        "facet_fields": [],
        "facet_queries": [],
    }
