import pytest


@pytest.fixture
def autocomplete_response():
    return {
        "responseHeader": {
            "QTime": 0,
            "params": {
                "mm": "100%",
                "q": "fanc",
                "defType": "edismax",
                "facet_min_count": "1",
                "hl": "false",
                "qf": "id^100 name^10 name_t^5 name_ac symbol^10 symbol_t^5 symbol_ac synonym synonym_t synonym_ac description_t xref",
                "start": "0",
                "q.op": "AND",
                "boost": 'product(if(termfreq(category,"biolink:PhenotypicFeature"),1.1,1),if(termfreq(category,"biolink:Disease"),1.3,1),if(and(termfreq(in_taxon,"NCBITaxon:9606"),termfreq(category,"biolink:Gene")),1.1,1),if(termfreq(deprecated,"true"),0.1,1))',
                "facet.mincount": "1",
                "rows": "10",
                "facet": "true",
            },
        },
        "response": {
            "num_found": 398,
            "start": 0,
            "docs": [
                {
                    "id": "MONDO:0009215",
                    "category": "biolink:Disease",
                    "name": "Fanconi anemia complementation group A",
                    "description": "Fanconi anemia caused by mutations of the FANCA gene. FANCA gene mutations are the most common cause of Fanconi anemia. This gene provides instructions for making a protein that is involved in the Fanconi anemia (FA) pathway.",
                    "provided_by": "phenio_nodes",
                    "xref": [
                        "DOID:0111095",
                        "GARD:15170",
                        "GTR:AN1051558",
                        "MEDGEN:483333",
                        "NCIT:C125702",
                        "OMIM:227650",
                        "UMLS:C3469521",
                    ],
                    "synonym": [
                        "Estren-Dameshek variant of Fanconi Anaemia",
                        "Estren-Dameshek variant of Fanconi Anemia",
                        "Estren-Dameshek variant of Fanconi pancytopenia",
                        "FANCA",
                        "FANCA Fanconi anaemia",
                        "FANCA Fanconi anemia",
                        "Fanconi Anaemia",
                        "Fanconi Anemia",
                        "Fanconi Anemia, Estren-Dameshek variant",
                        "Fanconi Anemia, complementation group type a",
                        "Fanconi anaemia caused by mutation in FANCA",
                        "Fanconi anaemia complementation group type A",
                        "Fanconi anemia caused by mutation in FANCA",
                        "Fanconi anemia complementation group A",
                        "Fanconi anemia complementation group type A",
                        "Fanconi anemia, complementation group A",
                    ],
                    "exact_synonyms": [
                        "FANCA|FANCA Fanconi anaemia|FANCA Fanconi anemia|Fanconi Anemia, complementation group type a|Fanconi anaemia caused by mutation in FANCA|Fanconi anaemia complementation group type A|Fanconi anemia caused by mutation in FANCA|Fanconi anemia complementation group A|Fanconi anemia complementation group type A"
                    ],
                    "related_synonyms": [
                        "Estren-Dameshek variant of Fanconi Anaemia|Estren-Dameshek variant of Fanconi Anemia|Estren-Dameshek variant of Fanconi pancytopenia|Fanconi Anaemia|Fanconi Anemia|Fanconi Anemia, Estren-Dameshek variant|Fanconi anemia, complementation group A"
                    ],
                    "subsets": ["clingen", "gard_rare", "nord_rare", "rare"],
                    "namespace": "MONDO",
                    "has_phenotype": [
                        "HP:0001875",
                        "HP:0001017",
                        "HP:0000104",
                        "HP:0003974",
                        "HP:0001876",
                        "HP:0000028",
                        "HP:0001873",
                        "HP:0009778",
                        "HP:0001896",
                        "HP:0009777",
                        "HP:0000568",
                        "HP:0001518",
                        "HP:0003221",
                        "HP:0001000",
                        "HP:0000252",
                        "HP:0001249",
                        "HP:0009943",
                        "HP:0001627",
                        "HP:0000978",
                        "HP:0030680",
                        "HP:0001903",
                        "HP:0000957",
                        "HP:0000815",
                        "HP:0001909",
                        "HP:0012210",
                        "HP:0000081",
                        "HP:0000085",
                        "HP:0000086",
                        "HP:0004322",
                        "HP:0000486",
                        "HP:0000365",
                        "HP:0003214",
                        "HP:0003213",
                        "HP:0003251",
                    ],
                    "has_phenotype_label": [
                        "Decreased total neutrophil count",
                        "Anemic pallor",
                        "Renal agenesis",
                        "Absent radius",
                        "Pancytopenia",
                        "Cryptorchidism",
                        "Thrombocytopenia",
                        "Short thumb",
                        "Reticulocytopenia",
                        "Absent thumb",
                        "Microphthalmia",
                        "Small for gestational age",
                        "Chromosomal breakage induced by crosslinking agents",
                        "Abnormality of skin pigmentation",
                        "Microcephaly",
                        "Intellectual disability",
                        "Complete duplication of thumb phalanx",
                        "Abnormal heart morphology",
                        "Bruising susceptibility",
                        "Abnormal cardiovascular system morphology",
                        "Anemia",
                        "Cafe-au-lait spot",
                        "Hypergonadotropic hypogonadism",
                        "Leukemia",
                        "Abnormal renal morphology",
                        "Duplicated collecting system",
                        "Horseshoe kidney",
                        "Ectopic kidney",
                        "Short stature",
                        "Strabismus",
                        "Hearing impairment",
                        "Prolonged G2 phase of cell cycle",
                        "Deficient excision of UV-induced pyrimidine dimers in DNA",
                        "Male infertility",
                    ],
                    "has_phenotype_count": 34,
                    "has_phenotype_closure": [
                        "HP:0000144",
                        "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:0080300",
                        "UPHENO:0076941",
                        "HP:0000085",
                        "UPHENO:0041465",
                        "UPHENO:0041226",
                        "UPHENO:0041629",
                        "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",
                        "UPHENO:0074584",
                        "UPHENO:0054970",
                        "UPHENO:0080662",
                        "HP:0000957",
                        "UPHENO:0074575",
                        "HP:0007400",
                        "HP:0012733",
                        "HP:0001034",
                        "HP:0000978",
                        "UPHENO:0002576",
                        "HP:0011276",
                        "UBERON:0011818",
                        "UBERON:0007798",
                        "UBERON:0000477",
                        "UPHENO:0003086",
                        "MPATH:603",
                        "UPHENO:0076810",
                        "UBERON:0004535",
                        "UPHENO:0081423",
                        "UBERON:0000948",
                        "UBERON:0005178",
                        "UPHENO:0002634",
                        "UBERON:0001009",
                        "HP:0012041",
                        "HP:0001903",
                        "HP:0030680",
                        "UBERON:0015228",
                        "UPHENO:9002003",
                        "HP:0009998",
                        "UBERON:0010688",
                        "UBERON:5106048",
                        "MPATH:1000",
                        "UBERON:0012151",
                        "UBERON:0015063",
                        "UBERON:0015204",
                        "UBERON:0003620",
                        "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",
                        "UPHENO:0002385",
                        "GO:0003008",
                        "UPHENO:0002267",
                        "UPHENO:0002269",
                        "GO:0050890",
                        "HP:0011446",
                        "UBERON:0002105",
                        "UPHENO:0002433",
                        "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",
                        "UBERON:0001016",
                        "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",
                        "UPHENO:0004523",
                        "UPHENO:0003001",
                        "HP:0011018",
                        "UPHENO:0003004",
                        "UPHENO:0002736",
                        "UPHENO:0076799",
                        "GO:0043473",
                        "UBERON:0001436",
                        "HP:0001000",
                        "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: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",
                        "UPHENO:0046624",
                        "HP:0001172",
                        "UBERON:0000307",
                        "UPHENO:0046750",
                        "UPHENO:0002905",
                        "UPHENO:0080114",
                        "UBERON:0001442",
                        "UBERON:0003056",
                        "UBERON:0012139",
                        "UBERON:0006048",
                        "HP:0012638",
                        "UPHENO:0086700",
                        "UBERON:0003071",
                        "UPHENO:0069674",
                        "UPHENO:0069684",
                        "UBERON:0012141",
                        "UPHENO:0084448",
                        "UBERON:0012150",
                        "UBERON:0012354",
                        "GO:0009892",
                        "HP:0011017",
                        "UBERON:0012140",
                        "HP:0004275",
                        "UPHENO:0069161",
                        "HP:0000118",
                        "UBERON:0000922",
                        "UBERON:0000923",
                        "UBERON:0006601",
                        "HP:0040068",
                        "UPHENO:0046445",
                        "UPHENO:0069327",
                        "UPHENO:0025544",
                        "UPHENO:0003093",
                        "HP:0004742",
                        "HP:0032309",
                        "UPHENO:0025509",
                        "UPHENO:0002902",
                        "UPHENO:0002559",
                        "UPHENO:0026023",
                        "HP:0003214",
                        "CL:0000255",
                        "UPHENO:0025808",
                        "UBERON:0004288",
                        "UPHENO:0025545",
                        "UPHENO:0080200",
                        "UPHENO:0002586",
                        "UPHENO:0002746",
                        "UPHENO:0003177",
                        "UBERON:0011137",
                        "UPHENO:0053563",
                        "UPHENO:0004595",
                        "UPHENO:0075944",
                        "UPHENO:0002983",
                        "UPHENO:0041821",
                        "HP:0002011",
                        "UBERON:0000465",
                        "UBERON:0004765",
                        "UPHENO:0010795",
                        "UPHENO:0004064",
                        "UBERON:0003221",
                        "UPHENO:0026806",
                        "HP:0040064",
                        "UPHENO:0011563",
                        "UPHENO:0003095",
                        "UPHENO:0087510",
                        "UPHENO:0026808",
                        "HP:0009822",
                        "UPHENO:0002945",
                        "UPHENO:0076718",
                        "UBERON:0011143",
                        "UPHENO:0003049",
                        "UPHENO:0002637",
                        "UPHENO:0002967",
                        "UPHENO:0049952",
                        "HP:0012443",
                        "UPHENO:0084763",
                        "UPHENO:0087660",
                        "UPHENO:0026317",
                        "UPHENO:0025136",
                        "UBERON:0000991",
                        "UPHENO:0076754",
                        "UBERON:0015212",
                        "GO:0065007",
                        "UBERON:0008785",
                        "UBERON:0019231",
                        "UPHENO:0008523",
                        "HP:0010935",
                        "UPHENO:0087501",
                        "UPHENO:0081451",
                        "HP:0000078",
                        "HP:0001626",
                        "UPHENO:0008604",
                        "HP:0008678",
                        "UBERON:0001008",
                        "UPHENO:0026811",
                        "UPHENO:0026506",
                        "UPHENO:0009011",
                        "UPHENO:0046552",
                        "UBERON:0011249",
                        "UBERON:0005177",
                        "UPHENO:0003025",
                        "UBERON:0000916",
                        "HP:0000951",
                        "UPHENO:0005596",
                        "UPHENO:0009129",
                        "HP:0000549",
                        "UPHENO:0004482",
                        "UPHENO:0076779",
                        "UPHENO:0005513",
                        "UPHENO:0009366",
                        "UPHENO:0004521",
                        "UPHENO:0026010",
                        "UPHENO:0025961",
                        "UPHENO:0004615",
                        "HP:0000079",
                        "UPHENO:0041075",
                        "UPHENO:3000003",
                        "UPHENO:0011817",
                        "UPHENO:0054957",
                        "UBERON:0034923",
                        "UPHENO:0085354",
                        "UPHENO:0011572",
                        "UBERON:0004122",
                        "UPHENO:0052165",
                        "UBERON:8450002",
                        "UBERON:0000026",
                        "UPHENO:0008827",
                        "UPHENO:0002642",
                        "UPHENO:0011749",
                        "UBERON:5102389",
                        "GO:0050794",
                        "UPHENO:0081466",
                        "UPHENO:0009209",
                        "UPHENO:0002553",
                        "NCBITaxon:33154",
                        "UPHENO:0026227",
                        "UPHENO:0018390",
                        "UPHENO:0088148",
                        "UPHENO:0026600",
                        "UPHENO:0026308",
                        "UPHENO:0011533",
                        "UPHENO:0087427",
                        "CL:0000738",
                        "UBERON:0003103",
                        "UPHENO:0002648",
                        "UBERON:0004375",
                        "HP:0031704",
                        "UPHENO:0002731",
                        "UPHENO:0026507",
                        "UPHENO:0002830",
                        "UPHENO:0054304",
                        "HP:0000077",
                        "GO:0019222",
                        "UPHENO:0087924",
                        "UPHENO:0002963",
                        "UPHENO:0003799",
                        "UPHENO:0002568",
                        "UPHENO:0080099",
                        "UPHENO:0009337",
                        "UPHENO:0087347",
                        "UPHENO:0004469",
                        "UPHENO:0080079",
                        "UPHENO:0077348",
                        "UPHENO:0027014",
                        "UPHENO:0002682",
                        "HP:0000234",
                        "UPHENO:0085356",
                        "BFO:0000040",
                        "UPHENO:0077418",
                        "UBERON:0007524",
                        "UBERON:0010230",
                        "UPHENO:0004892",
                        "UPHENO:0002926",
                        "UPHENO:0063794",
                        "HP:0005922",
                        "UPHENO:0086176",
                        "HP:0000104",
                        "UPHENO:0002738",
                        "HP:0011893",
                        "UPHENO:0004704",
                        "UBERON:0010371",
                        "UBERON:0002100",
                        "UPHENO:0082794",
                        "UPHENO:0004476",
                        "UBERON:0002091",
                        "UBERON:0004357",
                        "UPHENO:0001002",
                        "UPHENO:0004621",
                        "UPHENO:0002536",
                        "CL:0000457",
                        "HP:0000486",
                        "HP:0001874",
                        "UPHENO:0005518",
                        "UPHENO:0025883",
                        "GO:0044238",
                        "GO:0042592",
                        "UBERON:0002470",
                        "UPHENO:0001003",
                        "UBERON:0002371",
                        "UPHENO:0005277",
                        "UPHENO:0025176",
                        "UPHENO:0002525",
                        "UPHENO:0052970",
                        "UBERON:0002199",
                        "GO:0031052",
                        "UPHENO:0026183",
                        "UBERON:0002193",
                        "UPHENO:3000004",
                        "UPHENO:0025187",
                        "HP:0002597",
                        "HP:0000001",
                        "UPHENO:0004885",
                        "UPHENO:0086589",
                        "HP:0011991",
                        "UPHENO:0080352",
                        "UBERON:0002417",
                        "UPHENO:0077373",
                        "UBERON:0000468",
                        "GO:0006281",
                        "HP:0011121",
                        "UPHENO:0011536",
                        "UPHENO:0069062",
                        "UPHENO:0066925",
                        "UBERON:0010314",
                        "UPHENO:0077399",
                        "HP:0000364",
                        "UPHENO:0004831",
                        "UPHENO:0004459",
                        "UBERON:0001460",
                        "UPHENO:0086172",
                        "UPHENO:0002948",
                        "UBERON:0002390",
                        "UPHENO:0049703",
                        "UPHENO:0027189",
                        "GO:0090304",
                        "UBERON:0010323",
                        "HP:0006503",
                        "UPHENO:0086485",
                        "CL:0000763",
                        "HP:0001881",
                        "HP:0000707",
                        "CL:0000766",
                        "UBERON:0004120",
                        "UBERON:0000383",
                        "UPHENO:0011770",
                        "UPHENO:0002554",
                        "UPHENO:0063787",
                        "UBERON:0002050",
                        "UPHENO:0025855",
                        "UPHENO:0026098",
                        "UBERON:0002386",
                        "UPHENO:0085330",
                        "HP:0011927",
                        "HP:0011844",
                        "UPHENO:0002880",
                        "CL:0000094",
                        "UPHENO:0026146",
                        "UBERON:0000915",
                        "HP:0000252",
                        "UPHENO:0026309",
                        "HP:0009943",
                        "UPHENO:0008640",
                        "UPHENO:0005141",
                        "HP:0000980",
                        "HP:0010974",
                        "UPHENO:0025135",
                        "UBERON:0034925",
                        "UBERON:0000467",
                        "UPHENO:0005092",
                        "UBERON:5006048",
                        "HP:0040072",
                        "UPHENO:0027631",
                        "CL:0000219",
                        "UPHENO:0077391",
                        "UBERON:0001062",
                        "UPHENO:0025652",
                        "UPHENO:0008668",
                        "UPHENO:0025661",
                        "UPHENO:0009356",
                        "UPHENO:0080126",
                        "HP:0000598",
                        "UPHENO:0081581",
                        "MPATH:0",
                        "UBERON:0006058",
                        "HP:0002813",
                        "UPHENO:0009020",
                        "UBERON:0010130",
                        "UPHENO:0076697",
                        "UPHENO:0086019",
                        "UPHENO:0025553",
                        "HP:0000081",
                        "UPHENO:0008487",
                        "UPHENO:0001001",
                        "UPHENO:0011498",
                        "UPHENO:0002754",
                        "UBERON:0000062",
                        "UPHENO:0079826",
                        "UBERON:0003075",
                        "UBERON:0004121",
                        "UPHENO:0026181",
                        "UPHENO:0049587",
                        "CL:0000225",
                        "UBERON:0000955",
                        "UPHENO:0085371",
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                        "UPHENO:0027017",
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                        "UBERON:0019221",
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                        "UPHENO:0026643",
                        "NBO:0000001",
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                        "UPHENO:0080209",
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                        "UPHENO:0026344",
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                        "HP:0045060",
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                        "UPHENO:0004827",
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                        "NCBITaxon:6072",
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                        "UBERON:0011676",
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                        "UPHENO:0066927",
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                        "HP:0001627",
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                        "NCBITaxon:1",
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                        "UBERON:0004456",
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                        "UPHENO:0005016",
                        "UPHENO:0012274",
                        "UBERON:0012358",
                        "UPHENO:0079872",
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                        "UBERON:0004128",
                        "UPHENO:0026096",
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                        "UBERON:0003102",
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                        "HP:0100542",
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                        "HP:0009778",
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                        "UBERON:0000479",
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                        "UPHENO:0003084",
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                        "UBERON:0000473",
                        "UPHENO:0002944",
                        "UPHENO:0002909",
                        "UBERON:0004053",
                        "MPATH:105",
                        "UPHENO:0054315",
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                        "UBERON:0003101",
                        "UPHENO:0004802",
                        "UBERON:0010758",
                        "UPHENO:0002597",
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                        "UPHENO:0002685",
                        "UPHENO:0075159",
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                        "HP:0000815",
                        "UPHENO:0053566",
                        "HP:0000789",
                        "UBERON:0000990",
                        "HP:0001933",
                        "UPHENO:0076723",
                        "HP:0002973",
                        "UBERON:0003607",
                        "HP:0010461",
                        "UPHENO:0053580",
                        "UPHENO:0027231",
                        "UBERON:0000079",
                        "NBO:0000313",
                        "UBERON:0010316",
                        "UPHENO:0002940",
                        "UPHENO:0081424",
                        "UPHENO:0003056",
                        "HP:0001872",
                        "UPHENO:0088166",
                        "HP:0009815",
                        "UBERON:0001015",
                        "HP:0001873",
                        "UPHENO:0050106",
                        "UPHENO:0066913",
                        "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": [
                        "Infertility",
                        "Male infertility",
                        "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",
                        "Horseshoe kidney",
                        "shape of anatomical entity phenotype",
                        "concave 3-D shape anatomical entity",
                        "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",
                        "Hyperpigmentation of the skin",
                        "Hypermelanotic macule",
                        "increased biological_process in skin of body",
                        "increased pigmentation",
                        "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",
                        "thoracic segment of trunk",
                        "Abnormality of the cardiovascular system",
                        "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 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",
                        "material anatomical entity physiology phenotype",
                        "multicellular organismal process",
                        "anatomical structure physiology phenotype",
                        "Abnormal nervous system physiology",
                        "nervous system process",
                        "thoracic segment organ phenotype",
                        "Abnormal skull morphology",
                        "Abnormality of skull size",
                        "Abnormality of the nervous system",
                        "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",
                        "cardiovascular system phenotype",
                        "anatomical system physiology phenotype",
                        "telencephalon morphology phenotype",
                        "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",
                        "nervous system physiology phenotype",
                        "forebrain 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",
                        "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",
                        "Decreased fertility",
                        "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",
                        "limb phenotype",
                        "musculoskeletal system phenotype",
                        "Macule",
                        "organ system subdivision",
                        "aplasia or hypoplasia of anatomical entity",
                        "absent abdominal segment element",
                        "Abnormality of the skin",
                        "germ layer phenotype",
                        "decreased size of the organism subdivision",
                        "absent bone element in the forelimb",
                        "lateral structure phenotype",
                        "surface structure",
                        "increased pigmentation in skin of body",
                        "radius bone phenotype",
                        "neurectoderm phenotype",
                        "male reproductive organ phenotype",
                        "absent compound organ",
                        "digit morphology phenotype",
                        "circulatory system phenotype",
                        "absent anatomical structure in the limb",
                        "ectoderm morphology phenotype",
                        "manus",
                        "renal system phenotype",
                        "Abnormal upper limb bone morphology",
                        "bone of pectoral complex phenotype",
                        "musculature phenotype",
                        "immune system",
                        "forelimb bud morphology phenotype",
                        "absent forelimb zeugopod bone in the forelimb",
                        "embryo phenotype",
                        "decreased length of organism subdivision",
                        "paired limb/fin segment",
                        "Puberty and gonadal disorders",
                        "decreased number of anatomical entity",
                        "digit 1 phenotype",
                        "forelimb bud",
                        "limb skeleton subdivision phenotype",
                        "absent anatomical entity in the tissue",
                        "manual digit 1 phalanx",
                        "reproductive system",
                        "blastula",
                        "skeletal system 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",
                        "appendage phenotype",
                        "absent bone of free limb or fin",
                        "absent anatomical structure in the forelimb",
                        "skeletal system morphology phenotype",
                        "Aplasia/Hypoplasia involving the central nervous system",
                        "absent limb bone in the forelimb",
                        "absent multicellular anatomical structure in the skeletal system",
                        "kinesthetic behavior",
                        "Aplasia involving forearm bones",
                        "Thrombocytopenia",
                        "absent forelimb zeugopod bone",
                        "skeleton",
                        "non-material anatomical boundary",
                        "skeletal element phenotype",
                        "presumptive structure phenotype",
                        "skeletal element",
                        "absent autopodial extension",
                        "lateral plate mesoderm",
                        "developing anatomical structure",
                        "phenotypic effect",
                        "aplasia or hypoplasia of radius bone",
                        "Opisthokonta",
                        "embryo morphology phenotype",
                        "size of eyeball of camera-type eye phenotype",
                        "absent skeletal element in the forelimb",
                        "paired limb/fin segment phenotype",
                        "Abnormal forebrain morphology",
                        "absent endochondral bone",
                        "trunk",
                        "Abnormality of the integument",
                        "absent forelimb endochondral element in the forelimb",
                        "abdomen element",
                        "absent material anatomical entity in the limb bud",
                        "Abnormal skeletal morphology",
                        "absent anatomical structure in the multicellular organism",
                        "anucleate cell",
                        "localised anatomical entity",
                        "absent abdominal segment element in the renal system",
                        "simple eye phenotype",
                        "multicellular organism phenotype",
                        "absent cavitated compound organ in the renal system",
                        "limb bud",
                        "Abnormality of the male genitalia",
                        "absent multicellular anatomical structure",
                        "organism subdivision",
                        "absent bone of pectoral complex",
                        "anatomical structure phenotype",
                        "absent limb bone",
                        "absent anatomical structure",
                        "organism subdivision phenotype",
                        "anatomical collection phenotype",
                        "anatomical entity morphology phenotype",
                        "biological_process phenotype",
                        "renal/urinary system phenotype",
                        "programmed DNA elimination by chromosome breakage",
                        "absent organ in the multicellular organism",
                        "absent anatomical structure in the renal system",
                        "Abnormality of the eye",
                        "Abnormality of the kidney",
                        "skin of body",
                        "negative regulation of gene expression phenotype",
                        "trunk region element phenotype",
                        "system process phenotype",
                        "enucleated reticulocyte",
                        "bone of appendage girdle complex",
                        "Decreased fertility in males",
                        "mesoderm-derived structure phenotype",
                        "gene expression",
                        "Abnormal morphology of the radius",
                        "subdivision of trunk phenotype",
                        "Short digit",
                        "number of anatomical enitites of type material anatomical entity phenotype",
                        "number of anatomical enitites of type compound organ phenotype",
                        "compound organ",
                        "kidney phenotype",
                        "decreased functionality of the material anatomical entity",
                        "absent endochondral element in the forelimb",
                        "increased qualitatively biological_process",
                        "Abnormal reproductive system morphology",
                        "Aplasia/Hypoplasia of the radius",
                        "Decreased total neutrophil count",
                        "germ layer / neural crest phenotype",
                        "decreased functionality of the anatomical structure",
                        "absent anatomical entity in the renal system",
                        "shape of continuant phenotype",
                        "absent long bone in the forelimb",
                        "upper urinary tract",
                        "interphase",
                        "absent arm bone in the forelimb",
                        "Renal agenesis",
                        "vestibulo-auditory system phenotype",
                        "renal system",
                        "cell",
                        "response to stress phenotype",
                        "number of anatomical enitites of type abdomen element phenotype",
                        "craniocervical region phenotype",
                        "compound organ phenotype",
                        "eukaryotic cell",
                        "upper limb segment phenotype",
                        "decreased qualitatively nervous system process",
                        "eye movement phenotype",
                        "paired limb/fin",
                        "decreased qualitatively biological_process",
                        "endochondral element",
                        "number of anatomical enitites of type cavitated compound organ phenotype",
                        "forelimb phenotype",
                        "Bruising susceptibility",
                        "blood cell",
                        "visual system phenotype",
                        "decreased number of material anatomical entity",
                        "ectoderm phenotype",
                        "subdivision of trunk",
                        "skeleton of digitopodium",
                        "cranial skeletal system",
                        "appendicular skeleton",
                        "regional part of brain phenotype",
                        "regulation of gene expression",
                        "absent radius endochondral element",
                        "musculoskeletal system",
                        "Leukemia",
                        "absent multicellular anatomical structure in the renal system",
                        "hematopoietic system phenotype",
                        "regulation of biological process",
                        "optic cup morphology phenotype",
                        "Abnormality of the skeletal system",
                        "Abnormality of the musculoskeletal system",
                        "manus morphology phenotype",
                        "absent limb endochondral element in the forelimb",
                        "germ layer",
                        "G2 phase",
                        "Microcephaly",
                        "absent compound organ in the renal system",
                        "Aplasia/hypoplasia involving bones of the extremities",
                        "decreased size of the eyeball of camera-type eye",
                        "granulocyte morphology phenotype",
                        "subdivision of organism along main body axis phenotype",
                        "absent organism subdivision",
                        "erythroid lineage cell morphology phenotype",
                        "number of hematopoietic cell phenotype",
                        "material entity",
                        "number of anatomical enitites of type lateral structure phenotype",
                        "kidney morphology phenotype",
                        "immune system phenotype",
                        "unilaminar epithelium",
                        "digit 1 or 5 phenotype",
                        "decreased number of myeloid cell",
                        "sensory system phenotype",
                        "neutrophil",
                        "granulocyte",
                        "multicellular organism",
                        "taxon specific phenotype",
                        "endocrine system",
                        "hemolymphoid system",
                        "absent abdomen element in the renal system",
                        "system process",
                        "number of anatomical enitites of type anatomical structure phenotype",
                        "absent anatomical entity in the limb bud",
                        "absent abdomen element",
                        "upper urinary tract phenotype",
                        "main body axis",
                        "skull morphology phenotype",
                        "programmed DNA elimination",
                        "orbital region",
                        "hematopoietic cell",
                        "Duplication of phalanx of hand",
                        "metabolic process phenotype",
                        "phenotype",
                        "ectoderm-derived structure",
                        "multicellular organism height phenotype",
                        "subdivision of head",
                        "All",
                        "shape of kidney phenotype",
                        "absent organ in the renal system",
                        "mesoderm phenotype",
                        "immune system morphology phenotype",
                        "myeloid cell",
                        "absent multicellular anatomical structure in the multicellular organism",
                        "absent anatomical entity in the multicellular organism",
                        "Absent radius",
                        "pathological phenotype observation",
                        "hematopoietic system",
                        "Phenotypic abnormality",
                        "limb skeleton subdivision",
                        "Abnormality of the urinary system",
                        "entity",
                        "decreased number of leukocyte",
                        "cavitated compound organ",
                        "manual digit phenotype",
                        "Abnormal leukocyte morphology",
                        "secretory cell",
                        "Abnormality of the upper urinary tract",
                        "number of anatomical enitites of type granulocyte phenotype",
                        "absent trunk region element in the renal system",
                        "absent anatomical entity",
                        "embryonic structure",
                        "anatomical entity",
                        "pigmentation phenotype",
                        "size of anatomical entity phenotype",
                        "neural tube morphology phenotype",
                        "bone of pectoral complex morphology phenotype",
                        "Abnormality of neutrophils",
                        "genitourinary system",
                        "limb long bone phenotype",
                        "multi-tissue structure phenotype",
                        "Abnormal cellular immune system morphology",
                        "DNA metabolic process",
                        "3-D shape anatomical entity",
                        "continuant",
                        "myeloid leukocyte phenotype",
                        "orbital region phenotype",
                        "Abnormality of the upper limb",
                        "Cafe-au-lait spot",
                        "number of anatomical enitites of type organism subdivision phenotype",
                        "musculature of body",
                        "trunk region element",
                        "behavior",
                        "number of cell phenotype",
                        "craniofacial/craniocervical phenotype",
                        "agenesis of anatomical entity",
                        "process",
                        "multicellular anatomical structure",
                        "biological phase",
                        "number of anatomical enitites of type anatomical entity phenotype",
                        "motile cell",
                        "long bone morphology phenotype",
                        "limb long bone",
                        "aplasia or hypoplasia of skeleton",
                        "Abnormal granulocyte count",
                        "number of anatomical enitites of type neutrophil phenotype",
                        "paired limb/fin bud phenotype",
                        "absent limb endochondral element in the limb",
                        "forelimb zeugopod skeleton",
                        "Abnormal total neutrophil count",
                        "Prolonged G2 phase of cell cycle",
                        "thoracic cavity element",
                        "anatomical entity phenotype",
                        "absent anatomical entity in the skeletal system",
                        "number of anatomical enitites of type endochondral bone phenotype",
                        "abdominal segment element phenotype",
                        "nucleate cell",
                        "material anatomical entity",
                        "number of anatomical enitites of type skeletal element phenotype",
                        "reproductive structure phenotype",
                        "circulatory system",
                        "autopod region",
                        "absent radius bone",
                        "skin of body morphology phenotype",
                        "phalanx",
                        "cell phenotype",
                        "number of myeloid cell phenotype",
                        "integument phenotype",
                        "Abnormality of the genital system",
                        "non-connected functional system",
                        "behavior process phenotype",
                        "forelimb long bone",
                        "nucleic acid metabolic process",
                        "number of leukocyte phenotype",
                        "cavitated compound organ phenotype",
                        "anatomical structure",
                        "Abnormal leukocyte count",
                        "limb segment phenotype",
                        "abdomen element phenotype",
                        "endochondral element phenotype",
                        "Abnormal renal morphology",
                        "subdivision of head phenotype",
                        "anterior region of body",
                        "absent endochondral element in the limb",
                        "absent bone element in the limb",
                        "absent multicellular anatomical structure in the limb",
                        "decreased number of hematopoietic cell",
                        "blood cell phenotype",
                        "anatomical system",
                        "pre-chordal neural plate phenotype",
                        "number of anatomical enitites of type trunk region element phenotype",
                        "leukocyte morphology phenotype",
                        "forelimb skeleton phenotype",
                        "Abnormal immune system morphology",
                        "absent lateral structure",
                        "ear",
                        "Abnormality of the ear",
                        "bone of appendage girdle complex phenotype",
                        "Abnormality of the immune system",
                        "Abnormal myeloid leukocyte morphology",
                        "independent continuant",
                        "decreased sensory perception",
                        "absent organ",
                        "Abnormal hand morphology",
                        "decreased number of anatomical structure",
                        "bone of free limb or fin phenotype",
                        "paired limb/fin skeleton phenotype",
                        "size of skull phenotype",
                        "growth phenotype",
                        "absent lateral structure in the renal system",
                        "absent material anatomical entity in the renal system",
                        "absent trunk region element in the multicellular organism",
                        "decreased length of manual digit 1",
                        "Abnormality of the genitourinary system",
                        "Abnormal ear physiology",
                        "Abnormal granulocyte morphology",
                        "structure with developmental contribution from neural crest",
                        "skin of body phenotype",
                        "body proper",
                        "absent forelimb long bone",
                        "gonad phenotype",
                        "appendicular skeletal system",
                        "macromolecule metabolic process phenotype",
                        "organ",
                        "camera-type eye",
                        "absent mesoderm-derived structure",
                        "integumental system phenotype",
                        "phalanx endochondral element",
                        "skeletal system",
                        "Abnormal bone marrow cell morphology",
                        "absent mesoderm-derived structure in the forelimb",
                        "paired limb/fin skeleton",
                        "Aplasia/Hypoplasia of fingers",
                        "abdomen",
                        "decreased size of the digit",
                        "surface structure phenotype",
                        "anatomical entity morphology in the manus phenotype",
                        "decreased number of granulocyte",
                        "forelimb bone phenotype",
                        "anatomical system phenotype",
                        "zeugopod",
                        "decreased number of neutrophil",
                        "biological_process",
                        "multi-limb segment region phenotype",
                        "number of anatomical enitites of type reticulocyte phenotype",
                        "kidney",
                        "zeugopodial skeleton",
                        "decreased number of cell",
                        "absent organ in the limb",
                        "material anatomical entity phenotype",
                        "appendicular skeleton phenotype",
                        "leukocyte",
                        "absent bone of appendage girdle complex in the forelimb",
                        "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",
                        "anatomical cluster phenotype",
                        "anatomical entity morphology in the skeleton of pectoral complex phenotype",
                        "ectoderm-derived structure phenotype",
                        "integumental system",
                        "absent kidney",
                        "skeleton phenotype",
                        "absent bone element",
                        "abdominal segment of trunk",
                        "body part movement",
                        "reproductive organ phenotype",
                        "number of platelet phenotype",
                        "excretory system",
                        "number of anatomical enitites of type kidney phenotype",
                        "neutrophil 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",
                        "tube phenotype",
                        "erythrocyte",
                        "pectoral appendage bud phenotype",
                        "number of anatomical enitites of type endochondral element phenotype",
                        "disconnected anatomical group",
                        "Abnormality of multiple cell lineages in the bone marrow",
                        "dense mesenchyme tissue",
                        "myeloid leukocyte",
                        "skeleton of limb",
                        "Hypogonadism",
                        "long bone phenotype",
                        "limb bud phenotype",
                        "Aplasia/hypoplasia involving bones of the upper limbs",
                        "Aplasia/hypoplasia involving the skeleton",
                        "Generalized abnormality of skin",
                        "absent mesoderm-derived structure in the multicellular organism",
                        "reproductive system phenotype",
                        "sensory perception phenotype",
                        "anatomical entity morphology in the pectoral complex phenotype",
                        "external genitalia",
                        "number of anatomical enitites of type bone element phenotype",
                        "ecto-epithelium phenotype",
                        "face morphology phenotype",
                        "autopodial extension",
                        "digit 1 digitopodial skeleton",
                        "absent material anatomical entity",
                        "tissue",
                        "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",
                        "manual digit 1",
                        "bone cell",
                        "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",
                        "absent forelimb bone",
                        "genitourinary system phenotype",
                        "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",
                        "system",
                        "Abnormal forearm morphology",
                        "limb bone phenotype",
                        "cell cycle phenotype",
                        "limb endochondral element phenotype",
                        "absent trunk region element",
                        "forelimb zeugopod phenotype",
                        "skeleton of manual digitopodium",
                        "abdominal segment element",
                        "serotonin secreting cell",
                        "forelimb endochondral element phenotype",
                        "phalanx of manus",
                        "limb bone morphology phenotype",
                        "forelimb bone",
                        "increased biological_process",
                        "endochondral bone phenotype",
                        "Abnormal male external genitalia morphology",
                        "forelimb zeugopod",
                        "eye movement",
                        "radius endochondral element",
                        "Abnormal localization of kidney",
                        "Abnormal heart morphology",
                        "absent mesoderm-derived structure in the limb",
                        "localised abdomen element",
                        "occurrent",
                        "limb morphology phenotype",
                        "localised male reproductive organ",
                        "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",
                        "arm bone",
                        "cellular response to stress phenotype",
                        "Pancytopenia",
                        "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",
                        "individual digit of digitopodial skeleton",
                        "pectoral appendage skeleton",
                        "aplastic anatomical entity",
                        "sense organ physiology phenotype",
                        "gonad",
                        "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",
                        "Renal hypoplasia/aplasia",
                        "integument",
                        "forelimb zeugopod bone morphology phenotype",
                        "anatomical entity dysfunction in independent continuant",
                        "paired limb/fin phenotype",
                        "localised reproductive organ",
                        "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",
                        "multi-limb segment region",
                        "Aplasia/Hypoplasia affecting the eye",
                        "multicellular anatomical structure phenotype",
                        "absent forelimb endochondral element",
                        "Hematological neoplasm",
                        "multicellular organism morphology phenotype",
                        "localised multicellular anatomical structure",
                        "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",
                        "organ system subdivision phenotype",
                        "lateral plate mesoderm morphology phenotype",
                        "Cryptorchidism",
                        "absent endochondral bone in the limb",
                        "autopod region morphology phenotype",
                        "oxygen accumulating cell",
                        "nervous system phenotype",
                        "platelet",
                        "lateral structure",
                        "bone marrow cell",
                        "decreased system process",
                        "neoplasm phenotype",
                        "biogenic amine secreting cell",
                        "location of anatomical entity phenotype",
                        "Abnormal external genitalia morphology",
                        "viscus",
                        "primordium",
                        "localised material anatomical entity",
                        "Abnormal testis morphology",
                        "localised gonad",
                        "cellular organisms",
                        "testis",
                        "external male genitalia",
                        "localised reproductive structure",
                        "size of multicellular organism phenotype",
                        "male organism phenotype",
                        "pigmentation",
                        "absent multicellular anatomical structure in the tissue",
                        "testis phenotype",
                        "male reproductive system phenotype",
                        "male reproductive system",
                        "localised anatomical structure",
                        "cognition",
                        "Morphological central nervous system abnormality",
                        "male organism",
                        "external genitalia phenotype",
                        "Abnormal skin morphology",
                        "external male genitalia phenotype",
                        "optic vesicle phenotype",
                        "localised testis",
                        "Abnormality of mental function",
                        "number of anatomical enitites of type organ phenotype",
                        "localised organ",
                        "male reproductive organ",
                        "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",
                        "anatomical entity physiology phenotype",
                        "programmed DNA elimination by chromosome breakage 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",
                    ],
                    "highlighting": None,
                },
                {
                    "id": "MONDO:0013566",
                    "category": "biolink:Disease",
                    "name": "Fanconi anemia complementation group L",
                    "description": "Any Fanconi anemia in which the cause of the disease is a mutation in the FANCL gene.",
                    "provided_by": "phenio_nodes",
                    "xref": ["DOID:0111082", "GARD:15754", "MEDGEN:854018", "OMIM:614083", "UMLS:C3469528"],
                    "synonym": [
                        "FANCL",
                        "FANCL Fanconi anaemia",
                        "FANCL Fanconi anemia",
                        "Fanconi Anemia, complementation Group 50",
                        "Fanconi Anemia, complementation group type 50",
                        "Fanconi anaemia caused by mutation in FANCL",
                        "Fanconi anaemia complementation group type L",
                        "Fanconi anemia caused by mutation in FANCL",
                        "Fanconi anemia complementation group L",
                        "Fanconi anemia complementation group type L",
                        "Fanconi anemia, complementation group L",
                    ],
                    "exact_synonyms": [
                        "FANCL|FANCL Fanconi anaemia|FANCL Fanconi anemia|Fanconi Anemia, complementation group type 50|Fanconi anaemia caused by mutation in FANCL|Fanconi anaemia complementation group type L|Fanconi anemia caused by mutation in FANCL|Fanconi anemia complementation group L|Fanconi anemia complementation group type L"
                    ],
                    "related_synonyms": [
                        "Fanconi Anemia, complementation Group 50|Fanconi anemia, complementation group L"
                    ],
                    "subsets": ["clingen", "gard_rare", "nord_rare", "otar", "rare"],
                    "namespace": "MONDO",
                    "has_phenotype": [
                        "HP:0001776",
                        "HP:0000369",
                        "HP:0000347",
                        "HP:0003974",
                        "HP:0000465",
                        "HP:0007018",
                        "HP:0001510",
                        "HP:0001511",
                        "HP:0009777",
                        "HP:0009892",
                        "HP:0004590",
                        "HP:0000151",
                        "HP:0001263",
                        "HP:0003221",
                        "HP:0002032",
                        "HP:0011968",
                        "HP:0001321",
                        "HP:0000175",
                        "HP:0000054",
                        "HP:0002575",
                        "HP:0000238",
                        "HP:0000437",
                        "HP:0000316",
                        "HP:0040012",
                        "HP:0008551",
                        "HP:0001903",
                        "HP:0000957",
                        "HP:0000122",
                        "HP:0002023",
                        "HP:0002188",
                        "HP:0000582",
                        "HP:0000568",
                        "HP:0000470",
                        "HP:0000431",
                        "HP:0005528",
                        "HP:0000089",
                    ],
                    "has_phenotype_label": [
                        "Bilateral talipes equinovarus",
                        "Low-set ears",
                        "Micrognathia",
                        "Absent radius",
                        "Webbed neck",
                        "Attention deficit hyperactivity disorder",
                        "Growth delay",
                        "Intrauterine growth retardation",
                        "Absent thumb",
                        "Anotia",
                        "Hypoplastic sacrum",
                        "Aplasia of the uterus",
                        "Global developmental delay",
                        "Chromosomal breakage induced by crosslinking agents",
                        "Esophageal atresia",
                        "Feeding difficulties",
                        "Cerebellar hypoplasia",
                        "Cleft palate",
                        "Micropenis",
                        "Tracheoesophageal fistula",
                        "Hydrocephalus",
                        "Depressed nasal tip",
                        "Hypertelorism",
                        "Chromosome breakage",
                        "Microtia",
                        "Anemia",
                        "Cafe-au-lait spot",
                        "Unilateral renal agenesis",
                        "Anal atresia",
                        "Delayed CNS myelination",
                        "Upslanted palpebral fissure",
                        "Microphthalmia",
                        "Short neck",
                        "Wide nasal bridge",
                        "Bone marrow hypocellularity",
                        "Renal hypoplasia",
                    ],
                    "has_phenotype_count": 36,
                    "has_phenotype_closure": [
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                        "UPHENO:9002003",
                        "UPHENO:0088047",
                        "UBERON:0007798",
                        "UPHENO:0068914",
                        "HP:0002973",
                        "UPHENO:0025570",
                        "UBERON:0001009",
                        "UBERON:0002390",
                        "HP:0003241",
                        "UPHENO:0014291",
                        "UPHENO:0056242",
                        "UBERON:0003061",
                        "UBERON:0003080",
                        "UBERON:0004535",
                        "UPHENO:0085938",
                        "UPHENO:0004064",
                        "UBERON:0013701",
                        "UPHENO:0002704",
                        "UPHENO:0004459",
                        "UBERON:0036302",
                        "UBERON:0006876",
                        "UBERON:0005629",
                        "HP:0002188",
                        "UPHENO:0056237",
                        "HP:0011297",
                        "NBO:0000313",
                        "UPHENO:0014320",
                        "UPHENO:0026630",
                        "UPHENO:0056250",
                        "UPHENO:0075877",
                        "UPHENO:0056158",
                        "UPHENO:0005230",
                        "UPHENO:0002987",
                        "UPHENO:0014351",
                        "UPHENO:0004418",
                        "UPHENO:0003236",
                        "UBERON:0008784",
                        "UPHENO:0005029",
                    ],
                    "has_phenotype_closure_label": [
                        "kidney hypoplasia",
                        "Renal hypoplasia",
                        "bone marrow",
                        "bone marrow cell",
                        "Bone marrow hypocellularity",
                        "Abnormal bone marrow cell morphology",
                        "Abnormality of multiple cell lineages in the bone marrow",
                        "increased size of the material anatomical entity",
                        "increased size of the ectoderm-derived structure",
                        "nasal bridge morphology phenotype",
                        "snout",
                        "nasal bridge phenotype",
                        "increased size of the anatomical structure",
                        "snout morphology phenotype",
                        "cervical region",
                        "vertebra phenotype",
                        "neck morphology phenotype",
                        "Short neck",
                        "trunk or cervical vertebra",
                        "trunk or cervical vertebra phenotype",
                        "cervical region of vertebral column",
                        "cervical vertebra",
                        "neck bone",
                        "dorsal part of neck",
                        "decreased length of multicellular anatomical structure",
                        "cervical vertebra endochondral element phenotype",
                        "decreased length of neck",
                        "decreased length of anatomical entity",
                        "vertebral element",
                        "decreased size of the material anatomical entity",
                        "size of eyeball of camera-type eye phenotype",
                        "decreased size of the multicellular anatomical structure",
                        "decreased size of the ectoderm-derived structure",
                        "aplasia or hypoplasia of eyeball of camera-type eye",
                        "Abnormality of globe size",
                        "decreased size of the anatomical structure",
                        "decreased size of the eyeball of camera-type eye",
                        "decreased size of the sense organ",
                        "Abnormal ocular adnexa morphology",
                        "palpebral fissure phenotype",
                        "Abnormal eyelid morphology",
                        "immune system",
                        "ocular adnexa",
                        "Upslanted palpebral fissure",
                        "Abnormality of the ocular adnexa",
                        "eyelid",
                        "optic cup morphology phenotype",
                        "camera-type eye morphology phenotype",
                        "biological_process in central nervous system phenotype",
                        "delayed central nervous system myelination",
                        "delayed ensheathment of neurons",
                        "delayed axon ensheathment",
                        "glial cell differentiation",
                        "glial cell development",
                        "cell differentiation",
                        "cell development",
                        "cellular developmental process",
                        "ensheathment of neurons",
                        "delayed axon ensheathment in central nervous system",
                        "delayed cellular process",
                        "oligodendrocyte development",
                        "central nervous system myelination",
                        "axon ensheathment phenotype",
                        "myelination phenotype",
                        "anatomical conduit atresia",
                        "decreased length of organism subdivision",
                        "ectoderm-derived structure atresia",
                        "Abnormality of the anus",
                        "anus phenotype",
                        "Anal atresia",
                        "absent abdominal segment element in the renal system",
                        "absent organ in the renal system",
                        "Abnormality of the kidney",
                        "absent compound organ in the renal system",
                        "Renal agenesis",
                        "absent abdomen element",
                        "number of anatomical enitites of type compound organ phenotype",
                        "Renal hypoplasia/aplasia",
                        "renal system",
                        "kidney phenotype",
                        "absent trunk region element",
                        "kidney morphology phenotype",
                        "Abnormality of the urinary system",
                        "absent anatomical entity in the renal system",
                        "number of anatomical enitites of type trunk region element phenotype",
                        "Delayed CNS myelination",
                        "number of anatomical enitites of type cavitated compound organ phenotype",
                        "Abnormality of the upper urinary tract",
                        "Unilateral renal agenesis",
                        "absent multicellular anatomical structure in the renal system",
                        "absent abdominal segment element",
                        "abdomen element",
                        "renal system morphology phenotype",
                        "absent cavitated compound organ in the renal system",
                        "absent compound organ",
                        "absent trunk region element in the renal system",
                        "cavitated compound organ phenotype",
                        "renal system phenotype",
                        "kidney",
                        "upper urinary tract",
                        "absent kidney",
                        "Cafe-au-lait spot",
                        "integument phenotype",
                        "integumental system",
                        "Hyperpigmentation of the skin",
                        "skin of body",
                        "integument",
                        "increased pigmentation in skin of body",
                        "Macule",
                        "increased qualitatively biological_process",
                        "increased biological_process in skin of body",
                        "skin of body phenotype",
                        "erythrocyte morphology phenotype",
                        "Anemia",
                        "erythrocyte",
                        "Abnormal erythrocyte morphology",
                        "Abnormality of blood and blood-forming tissues",
                        "hematopoietic cell",
                        "oxygen accumulating cell",
                        "Microtia",
                        "external ear hypoplasia",
                        "immature eye",
                        "anatomical entity length phenotype",
                        "anatomical line between pupils",
                        "Microphthalmia",
                        "increased length of the immaterial anatomical entity",
                        "optic vesicle phenotype",
                        "increased size of the anatomical entity",
                        "immature eye phenotype",
                        "increased length of the anatomical line between pupils",
                        "non-material anatomical boundary",
                        "optic vesicle",
                        "increased length of the anatomical line",
                        "increased size of the non-material anatomical boundary",
                        "simple eye",
                        "non-material anatomical boundary phenotype",
                        "visual system",
                        "orbital region phenotype",
                        "anatomical line",
                        "simple eye phenotype",
                        "non-neural ectoderm phenotype",
                        "olfactory placode",
                        "Slanting of the palpebral fissure",
                        "Abnormal external nose morphology",
                        "neurogenic placode",
                        "external nose morphology phenotype",
                        "cranial placode phenotype",
                        "shape of nose tip phenotype",
                        "external soft tissue zone",
                        "Depressed nasal tip",
                        "neurogenic placode phenotype",
                        "olfactory placode morphology phenotype",
                        "increased biological_process",
                        "flattened anatomical entity",
                        "anatomical point",
                        "ectodermal placode phenotype",
                        "flat nose tip",
                        "non-neural ectoderm",
                        "Abnormal nasal morphology",
                        "Abnormal renal morphology",
                        "flat anatomical entity",
                        "olfactory organ phenotype",
                        "ectodermal placode",
                        "pre-chordal neural plate",
                        "bodily fluid",
                        "increased number of organ part in the cerebrospinal fluid",
                        "curvature anatomical entity",
                        "increased number of organ component layer",
                        "hematopoietic system",
                        "vascular system",
                        "blood",
                        "organism substance phenotype",
                        "number of anatomical enitites of type organ component layer phenotype",
                        "Abnormal cerebrospinal fluid morphology",
                        "increased length of the non-material anatomical boundary",
                        "ventricle of nervous system phenotype",
                        "nervous system",
                        "absent endochondral element",
                        "subdivision of digestive tract phenotype",
                        "dorsum",
                        "Hyperactivity",
                        "Localized skin lesion",
                        "nose phenotype",
                        "sensation behavior",
                        "decreased length of anatomical structure",
                        "Abnormality of chromosome stability",
                        "neck",
                        "neck phenotype",
                        "arm bone phenotype",
                        "appendicular skeletal system",
                        "absent limb long bone in the forelimb",
                        "Abnormality of the cervical spine",
                        "regulation of macromolecule biosynthetic process",
                        "Aplasia/hypoplasia of the extremities",
                        "forelimb zeugopod bone phenotype",
                        "trachea",
                        "increased number of ectoderm-derived structure in the cerebrospinal fluid",
                        "Abnormal penis morphology",
                        "absent forelimb long bone",
                        "decreased size of the organ",
                        "Aplasia/hypoplasia involving bones of the extremities",
                        "appendicular skeleton morphology phenotype",
                        "absent limb long bone",
                        "absent material anatomical entity in the forelimb",
                        "absent endochondral bone in the forelimb",
                        "Absent thumb",
                        "cranial skeletal system",
                        "skeleton of pectoral complex",
                        "Aplasia/hypoplasia involving forearm bones",
                        "myeloid cell",
                        "limb long bone morphology phenotype",
                        "pigmentation",
                        "radius endochondral element",
                        "pelvic appendage bud",
                        "forelimb zeugopod",
                        "forelimb bone",
                        "tissue",
                        "limb endochondral element phenotype",
                        "limb bone phenotype",
                        "Abnormal forearm morphology",
                        "system",
                        "Neurodevelopmental abnormality",
                        "absent arm bone",
                        "absent material anatomical entity in the tissue",
                        "Abnormality of the digestive system",
                        "absent anatomical structure in the tissue",
                        "absent anatomical entity in the limb",
                        "forelimb bud phenotype",
                        "skeleton of limb phenotype",
                        "sacral region",
                        "genitourinary system",
                        "forelimb zeugopod skeleton",
                        "axon ensheathment in central nervous system",
                        "absent limb endochondral element in the limb",
                        "manual digit 1 plus metapodial segment",
                        "eye phenotype",
                        "limb bone",
                        "Abnormality of head or neck",
                        "aplastic anatomical entity",
                        "anatomical structure atresia",
                        "bone of pectoral complex",
                        "decreased qualitatively embryo development",
                        "number of anatomical enitites of type mesoderm-derived structure phenotype",
                        "zeugopod phenotype",
                        "ensheathment of neurons phenotype",
                        "upper limb segment phenotype",
                        "Abnormal appendicular skeleton morphology",
                        "forelimb zeugopod morphology phenotype",
                        "absent lateral structure in the renal system",
                        "absent radius endochondral element in the forelimb",
                        "absent material anatomical entity in the reproductive system",
                        "absent bone of free limb or fin in the limb",
                        "absent multicellular anatomical structure in the forelimb",
                        "lateral plate mesoderm phenotype",
                        "endo-epithelium",
                        "absent bone of free limb or fin in the forelimb",
                        "central nervous system development",
                        "number of anatomical enitites of type bone element phenotype",
                        "Aplasia/hypoplasia involving bones of the upper limbs",
                        "Abnormal forearm bone morphology",
                        "long bone phenotype",
                        "absent material anatomical entity",
                        "Abnormality of the female genitalia",
                        "number of anatomical enitites of type endochondral element phenotype",
                        "absent organ in the tissue",
                        "intromittent organ",
                        "external nose",
                        "arm",
                        "absent lateral structure in the head",
                        "subdivision of tube atresia",
                        "endochondral bone",
                        "primary subdivision of cranial skeletal system phenotype",
                        "respiratory system",
                        "bodily fluid phenotype",
                        "bone of appendage girdle complex",
                        "absent multicellular anatomical structure in the multicellular organism",
                        "limb segment phenotype",
                        "Hypoplasia of penis",
                        "absent material anatomical entity in the limb",
                        "vision/eye phenotype",
                        "sclerotome",
                        "absent mesoderm-derived structure in the forelimb",
                        "absent endochondral element in the forelimb",
                        "increased width of nasal bridge",
                        "limb long bone phenotype",
                        "chordal neural plate phenotype",
                        "incomplete closing of the ectoderm-derived structure",
                        "absent forelimb zeugopod bone in the forelimb",
                        "Abnormal tracheobronchial morphology",
                        "absent radius endochondral element",
                        "absent material anatomical entity in the renal system",
                        "regulation of gene expression",
                        "absent anatomical structure in the forelimb",
                        "ectoderm-derived structure phenotype",
                        "absent anatomical structure in the multicellular organism",
                        "anatomical cluster phenotype",
                        "organ subunit phenotype",
                        "forelimb skeleton phenotype",
                        "absent lateral structure",
                        "radius bone phenotype",
                        "Abnormal male external genitalia morphology",
                        "increased number of multicellular anatomical structure",
                        "absent anatomical structure in the limb",
                        "organ part phenotype",
                        "circulatory system phenotype",
                        "appendicular skeleton",
                        "limb skeleton subdivision phenotype",
                        "bony pelvis",
                        "brain ventricle",
                        "reproductive organ",
                        "absent anatomical entity in the tissue",
                        "metencephalon morphology phenotype",
                        "absent bone element",
                        "axon ensheathment",
                        "abdominal segment of trunk",
                        "Abnormality of the upper limb",
                        "absent forelimb zeugopod bone",
                        "endochondral element",
                        "absent reproductive structure",
                        "lateral plate mesoderm",
                        "absent autopodial extension",
                        "cavitated compound organ",
                        "Aplasia involving forearm bones",
                        "absent multicellular anatomical structure in the skeletal system",
                        "vertebra",
                        "mesoderm-derived structure",
                        "delayed biological_process in central nervous system",
                        "forelimb skeleton",
                        "absent long bone in the forelimb",
                        "mesenchyme morphology phenotype",
                        "shape of continuant phenotype",
                        "number of anatomical enitites of type endochondral bone phenotype",
                        "absent radius bone",
                        "Absent forearm bone",
                        "digit 1 plus metapodial segment",
                        "absent organ",
                        "embryo development",
                        "Aplasia/Hypoplasia of the cerebellum",
                        "absent forelimb endochondral element in the forelimb",
                        "dorsal region element phenotype",
                        "Eumetazoa",
                        "absent anatomical entity in the female reproductive system",
                        "anatomical entity morphology in the skeleton of pectoral complex phenotype",
                        "gastrula morphology phenotype",
                        "haemolymphatic fluid phenotype",
                        "skeleton of lower jaw phenotype",
                        "absent organ in the multicellular organism",
                        "programmed DNA elimination by chromosome breakage",
                        "Abnormality of the eye",
                        "gastrula",
                        "multicellular organismal process phenotype",
                        "blastula",
                        "digestive tract",
                        "anatomical point phenotype",
                        "number of anatomical enitites of type material anatomical entity phenotype",
                        "intromittent organ phenotype",
                        "bone of jaw",
                        "abdomen element phenotype",
                        "foregut morphology phenotype",
                        "visual system phenotype",
                        "organ system subdivision",
                        "absent mesoderm-derived structure in the limb",
                        "mandible phenotype",
                        "bone element phenotype",
                        "Abnormal mandible morphology",
                        "digit phenotype",
                        "Abnormal skeletal morphology",
                        "skeleton of manus",
                        "lower jaw region",
                        "anatomical system phenotype",
                        "epithelium",
                        "absent reproductive structure in the female reproductive system",
                        "digestive system",
                        "multi-tissue structure phenotype",
                        "mandible hypoplasia",
                        "gene expression",
                        "absent limb endochondral element",
                        "head bone phenotype",
                        "aplasia or hypoplasia of mandible",
                        "axial skeleton plus cranial skeleton",
                        "pelvic appendage bud phenotype",
                        "negative regulation of gene expression",
                        "internal female genitalia phenotype",
                        "absent material anatomical entity in the multicellular organism",
                        "bone of lower jaw phenotype",
                        "anus morphology phenotype",
                        "germ layer phenotype",
                        "pectoral appendage skeleton",
                        "skeleton of lower jaw",
                        "absent mesoderm-derived structure",
                        "absent bone of pectoral complex in the forelimb",
                        "postcranial axial skeletal system",
                        "secondary palate morphology phenotype",
                        "skull",
                        "cell condensation phenotype",
                        "subdivision of tube phenotype",
                        "bone element hypoplasia in face",
                        "Abnormal jaw morphology",
                        "ventricle of nervous system",
                        "dermal bone phenotype",
                        "subdivision of organism along main body axis phenotype",
                        "Abnormal sacrum morphology",
                        "protuberance phenotype",
                        "aplasia or hypoplasia of skull",
                        "pharyngeal arch 1 phenotype",
                        "pectoral appendage",
                        "Abnormality of the lower limb",
                        "neural crest morphology phenotype",
                        "primary subdivision of skull phenotype",
                        "neural plate phenotype",
                        "absent bone of pectoral complex in the limb",
                        "decreased qualitatively multicellular organismal process",
                        "axial skeleton plus cranial skeleton phenotype",
                        "immaterial anatomical entity",
                        "bone of appendage girdle complex phenotype",
                        "Abnormality of the ear",
                        "regional part of brain phenotype",
                        "Abnormally increased volition",
                        "facial bone",
                        "absent endochondral bone",
                        "developing mesenchymal condensation",
                        "absent manual digit",
                        "limb bone morphology phenotype",
                        "dentary phenotype",
                        "absent anatomical entity in the limb bud",
                        "absent forelimb bone in the limb",
                        "anatomical entity hypoplasia",
                        "forelimb endochondral element",
                        "facial skeleton morphology phenotype",
                        "epithelium phenotype",
                        "absent organ in the limb",
                        "sacral region of vertebral column",
                        "embryonic tissue",
                        "mouth phenotype",
                        "dermal bone",
                        "skeletal system",
                        "radius bone morphology phenotype",
                        "limb",
                        "craniocervical region phenotype",
                        "compound organ phenotype",
                        "pectoral complex",
                        "subdivision of head phenotype",
                        "forelimb bone phenotype",
                        "anterior region of body",
                        "limb bud",
                        "multicellular organism phenotype",
                        "skin of body morphology phenotype",
                        "zone of organ phenotype",
                        "nose tip morphology phenotype",
                        "organ",
                        "absent forelimb endochondral element",
                        "absent multicellular anatomical structure in the limb",
                        "Abnormal cerebellum morphology",
                        "ear morphology phenotype",
                        "Micropenis",
                        "decreased developmental process",
                        "shape of external ear phenotype",
                        "neck bone phenotype",
                        "bone of pectoral complex morphology phenotype",
                        "neural tube morphology phenotype",
                        "absent forelimb long bone in the forelimb",
                        "increased length of the anatomical entity",
                        "subdivision of organism along main body axis",
                        "germ layer morphology phenotype",
                        "zeugopod",
                        "Abnormal nasal bridge morphology",
                        "foregut",
                        "absent bone of pectoral complex",
                        "anatomical structure phenotype",
                        "Abnormal affect",
                        "nose",
                        "absent limb bone in the forelimb",
                        "Aplasia/Hypoplasia involving the central nervous system",
                        "Abnormal upper limb bone morphology",
                        "pharyngeal arch phenotype",
                        "appendage",
                        "Abnormality of the palpebral fissures",
                        "forelimb long bone",
                        "facial skeleton phenotype",
                        "increased number of material anatomical entity",
                        "behavior process phenotype",
                        "subdivision of vertebral column phenotype",
                        "non-connected functional system",
                        "upper urinary tract phenotype",
                        "manual digit 1 or 5",
                        "migrating mesenchyme population",
                        "roof of mouth morphology phenotype",
                        "external nose phenotype",
                        "somite",
                        "decreased size of the organism subdivision",
                        "Abdominal symptom",
                        "forelimb zeugopod bone",
                        "bone element",
                        "central nervous system myelination phenotype",
                        "structure with developmental contribution from neural crest phenotype",
                        "subdivision of head",
                        "All",
                        "nose morphology phenotype",
                        "occurrent",
                        "multicellular anatomical structure",
                        "process",
                        "eye",
                        "sense organ phenotype",
                        "Abnormal CNS myelination",
                        "external ear phenotype",
                        "lateral structure",
                        "cerebellum morphology phenotype",
                        "Aplasia/Hypoplasia involving bones of the skull",
                        "erythroid lineage cell",
                        "limb bud morphology phenotype",
                        "Abnormal ear morphology",
                        "thoracic cavity element atresia",
                        "appendage girdle complex",
                        "eyeball of camera-type eye phenotype",
                        "limb bud phenotype",
                        "palpebral fissure",
                        "absent arm bone in the forelimb",
                        "hindlimb bud",
                        "hindlimb",
                        "pectoral appendage phenotype",
                        "Abnormal finger morphology",
                        "subdivision of trunk",
                        "material anatomical entity phenotype",
                        "future nervous system",
                        "intramembranous bone",
                        "embryonic structure phenotype",
                        "multi-limb segment region phenotype",
                        "biological_process",
                        "surface structure phenotype",
                        "shape of anatomical entity phenotype",
                        "incomplete closing of the multi-tissue structure",
                        "anatomical structure",
                        "absent anatomical entity in the skeletal system",
                        "subdivision of skeleton",
                        "anatomical entity phenotype",
                        "thoracic cavity element",
                        "absent forelimb bone",
                        "olfactory organ",
                        "pes phenotype",
                        "autopod region phenotype",
                        "main body axis",
                        "pes",
                        "continuant",
                        "Webbed neck",
                        "eyeball of camera-type eye",
                        "digestive system physiology phenotype",
                        "eukaryotic cell",
                        "germ layer",
                        "absent limb bone",
                        "anatomical wall",
                        "Abnormal anus morphology",
                        "Bilateral talipes equinovarus",
                        "hindlimb bud phenotype",
                        "oral opening",
                        "thoracic segment organ atresia",
                        "segment of autopod",
                        "face",
                        "Decreased anatomical entity position",
                        "entity",
                        "immaterial anatomical entity phenotype",
                        "hindlimb morphology phenotype",
                        "arm phenotype",
                        "Abnormality of digestive system physiology",
                        "Hydrocephalus",
                        "axial skeletal system",
                        "multicellular organism",
                        "Abnormal thumb morphology",
                        "long bone morphology phenotype",
                        "limb long bone",
                        "blood cell phenotype",
                        "subdivision of skeleton phenotype",
                        "embryo phenotype",
                        "ventricular system of brain",
                        "hindlimb bud morphology phenotype",
                        "number of anatomical enitites of type anatomical entity phenotype",
                        "absent anatomical structure",
                        "neural crest-derived structure phenotype",
                        "Abnormal pinna morphology",
                        "internal genitalia phenotype",
                        "body proper",
                        "organ part atresia",
                        "anatomical entity",
                        "embryonic structure",
                        "Abnormality of the neck",
                        "vestibulo-auditory system",
                        "paired limb/fin skeleton",
                        "haemolymphatic fluid",
                        "absent limb bone in the limb",
                        "pharyngeal arch",
                        "mandibular prominence morphology phenotype",
                        "paired limb/fin bud phenotype",
                        "limb segment",
                        "paired limb/fin",
                        "forelimb zeugopod phenotype",
                        "esophagus phenotype",
                        "reproductive system",
                        "absent reproductive structure in the reproductive system",
                        "respiratory system phenotype",
                        "number of anatomical enitites of type kidney phenotype",
                        "mesoderm phenotype",
                        "sense organ",
                        "vasculature phenotype",
                        "increased size of the immaterial anatomical entity",
                        "ear",
                        "neurectoderm phenotype",
                        "male reproductive organ phenotype",
                        "orifice",
                        "posterior region of body",
                        "limb morphology phenotype",
                        "Abnormality of limb bone",
                        "lower limb segment",
                        "manus morphology phenotype",
                        "neural crest-derived structure",
                        "ecto-epithelium phenotype",
                        "face morphology phenotype",
                        "autopodial extension",
                        "increased number of brain ventricle",
                        "anus",
                        "dermal skeletal element phenotype",
                        "telencephalon phenotype",
                        "phenotype",
                        "metabolic process phenotype",
                        "limb phenotype",
                        "appendage phenotype",
                        "olfactory placode phenotype",
                        "head phenotype",
                        "camera-type eye",
                        "bone of free limb or fin",
                        "increased width of anatomical structure",
                        "pigmentation phenotype",
                        "leg phenotype",
                        "Abnormality of the nose",
                        "absent multicellular anatomical structure",
                        "Abnormality of the male genitalia",
                        "organism subdivision",
                        "multi-tissue structure",
                        "system development",
                        "absent skeletal element",
                        "myelination",
                        "blood cell",
                        "postcranial axial skeleton",
                        "anatomical conduit",
                        "location of anatomical entity phenotype",
                        "absent endochondral bone in the limb",
                        "autopod region morphology phenotype",
                        "mesoderm-derived structure phenotype",
                        "number of anatomical enitites of type skeletal element phenotype",
                        "closing of the anatomical entity",
                        "material anatomical entity",
                        "vascular plexus phenotype",
                        "absent bone of free limb or fin",
                        "bone of craniocervical region",
                        "gliogenesis",
                        "head bone morphology phenotype",
                        "forelimb morphology phenotype",
                        "pes morphology phenotype",
                        "phenotypic effect",
                        "embryo development rate phenotype",
                        "Abnormality of the respiratory system",
                        "absent bone element in the forelimb",
                        "orbital region",
                        "limb skeleton subdivision",
                        "absent skeletal element in the forelimb",
                        "absent limb endochondral element in the forelimb",
                        "Disinhibition",
                        "developing anatomical structure",
                        "jaw region",
                        "Phenotypic abnormality",
                        "limb endochondral element",
                        "neural plate",
                        "paired limb/fin bud",
                        "integumental system phenotype",
                        "organ phenotype",
                        "tube phenotype",
                        "vertebral element phenotype",
                        "increased number of organ component layer in the cerebrospinal fluid",
                        "erythroid lineage cell morphology phenotype",
                        "lateral plate mesoderm morphology phenotype",
                        "skeleton of limb",
                        "organ system subdivision phenotype",
                        "Abnormal hand morphology",
                        "nose tip phenotype",
                        "vasculature of central nervous system plus retina phenotype",
                        "aplasia or hypoplasia of anatomical entity",
                        "primary subdivision of cranial skeletal system",
                        "absent anatomical structure in the skeletal system",
                        "decreased qualitatively biological_process",
                        "musculature of body",
                        "number of anatomical enitites of type organism subdivision phenotype",
                        "trunk mesenchyme phenotype",
                        "independent continuant",
                        "eye primordium",
                        "organ component layer phenotype",
                        "Abnormality of limbs",
                        "abdomen",
                        "developing anatomical structure phenotype",
                        "subdivision of digestive tract",
                        "face phenotype",
                        "regional part of nervous system phenotype",
                        "genitourinary system phenotype",
                        "pelvic appendage",
                        "embryonic tissue phenotype",
                        "absent material anatomical entity in the ear",
                        "entire sense organ system",
                        "Abnormal digit morphology",
                        "macromolecule metabolic process phenotype",
                        "lower limb segment phenotype",
                        "absent multicellular anatomical structure in the female reproductive system",
                        "forelimb zeugopod bone morphology phenotype",
                        "cell",
                        "skeletal system morphology phenotype",
                        "anatomical entity morphology in the pectoral complex phenotype",
                        "Abnormal respiratory system morphology",
                        "vestibulo-auditory system phenotype",
                        "cranial placode",
                        "external ear",
                        "multi organ part structure phenotype",
                        "increased pigmentation",
                        "presumptive ectoderm phenotype",
                        "ear phenotype",
                        "dermal skeleton phenotype",
                        "aplasia or hypoplasia of skeleton",
                        "cellular organisms",
                        "multi organ part structure",
                        "absent anatomical entity in the multicellular organism",
                        "membrane bone phenotype",
                        "embryonic tissue morphology phenotype",
                        "system process",
                        "orifice phenotype",
                        "digestive system morphology phenotype",
                        "Abnormal external genitalia morphology",
                        "long bone",
                        "pelvic appendage phenotype",
                        "facial bone hypoplasia",
                        "opening of the anatomical entity",
                        "paired limb/fin phenotype",
                        "Abnormality of the outer ear",
                        "anatomical entity physiology phenotype",
                        "anus atresia",
                        "programmed DNA elimination by chromosome breakage phenotype",
                        "musculoskeletal system",
                        "Cerebellar hypoplasia",
                        "absent forelimb bone in the forelimb",
                        "neural groove",
                        "upper limb segment",
                        "arm bone",
                        "increased number of brain ventricle in the cerebrospinal fluid",
                        "Abnormal limb bone morphology",
                        "neurectoderm",
                        "dentary",
                        "macromolecule biosynthetic process",
                        "skeletal element",
                        "tissue phenotype",
                        "neural crest phenotype",
                        "presumptive structure phenotype",
                        "skeletal element phenotype",
                        "skeleton",
                        "ectoderm",
                        "respiratory system morphology phenotype",
                        "closing of the thoracic segment organ",
                        "location of external ear phenotype",
                        "external ear morphology phenotype",
                        "Hypermelanotic macule",
                        "hindbrain phenotype",
                        "decreased length of material anatomical entity",
                        "neural plate morphology phenotype",
                        "anatomical system atresia",
                        "mandible morphology phenotype",
                        "vasculature of organ phenotype",
                        "musculoskeletal system phenotype",
                        "embryonic craniocervical region",
                        "irregular bone phenotype",
                        "mouth",
                        "delayed myelination",
                        "dermal skeletal element",
                        "forelimb bud morphology phenotype",
                        "digit 1",
                        "musculature phenotype",
                        "digit 1 or 5",
                        "radius bone",
                        "surface structure",
                        "aplastic forelimb zeugopod bone",
                        "Low-set ears",
                        "presumptive ectoderm",
                        "organ part",
                        "social inhibition",
                        "neural fold phenotype",
                        "neural crest",
                        "ectoderm morphology phenotype",
                        "embryonic autopod plate morphology phenotype",
                        "manus",
                        "Abnormality of the head",
                        "Irregular hyperpigmentation",
                        "decreased qualitatively behavior",
                        "negative regulation of cellular process",
                        "epithelial fold phenotype",
                        "anatomical system",
                        "head morphology phenotype",
                        "sensory system",
                        "pectoral appendage skeleton phenotype",
                        "ectoderm-derived structure",
                        "organ component layer",
                        "absent mesoderm-derived structure in the multicellular organism",
                        "reproductive system phenotype",
                        "cervical vertebra phenotype",
                        "epithelial fold",
                        "paired limb/fin skeleton phenotype",
                        "forelimb phenotype",
                        "external male genitalia",
                        "bone of free limb or fin phenotype",
                        "manual digit",
                        "skull morphology phenotype",
                        "programmed DNA elimination",
                        "Abnormal facial skeleton morphology",
                        "dermatocranium phenotype",
                        "pharyngeal arch 1 morphology phenotype",
                        "jaw skeleton",
                        "location of ear phenotype",
                        "Abnormality of skin pigmentation",
                        "absent uterus",
                        "eyelid morphology phenotype",
                        "pharyngeal region of foregut",
                        "dense mesenchyme tissue phenotype",
                        "Abnormality of the skeletal system",
                        "number of anatomical enitites of type abdominal segment element phenotype",
                        "regulation of biological process",
                        "Abnormal gastrointestinal tract morphology",
                        "Opisthokonta",
                        "Abnormal nasal tip morphology",
                        "foregut phenotype",
                        "anatomical collection phenotype",
                        "female reproductive system morphology phenotype",
                        "membrane bone",
                        "tracheobronchial tree",
                        "anatomical entity morphology phenotype",
                        "organism subdivision phenotype",
                        "forelimb endochondral element phenotype",
                        "increased number of brain ventricle/choroid plexus in the cerebrospinal fluid",
                        "absent anatomical structure in the renal system",
                        "craniofacial/craniocervical phenotype",
                        "agenesis of anatomical entity",
                        "neural fold",
                        "digit morphology phenotype",
                        "Eukaryota",
                        "embryo",
                        "future central nervous system",
                        "hindlimb phenotype",
                        "Talipes equinovarus",
                        "neural groove phenotype",
                        "bone cell",
                        "ecto-epithelium",
                        "aplasia or hypoplasia of radius bone",
                        "jaw skeleton morphology phenotype",
                        "anatomical entity hypoplasia in face",
                        "Aplasia/Hypoplasia of the radius",
                        "closing of the anatomical conduit",
                        "number of anatomical enitites of type multicellular anatomical structure phenotype",
                        "germ layer / neural crest phenotype",
                        "increased size of the anatomical line",
                        "forelimb",
                        "lateral structure phenotype",
                        "forelimb bud",
                        "digestive system element atresia",
                        "Aplasia/hypoplasia affecting bones of the axial skeleton",
                        "anterior neural tube",
                        "skull phenotype",
                        "alimentary part of gastrointestinal system morphology phenotype",
                        "Abnormal myelination",
                        "appendicular skeleton phenotype",
                        "primary subdivision of skull",
                        "Tracheoesophageal fistula",
                        "craniocervical region",
                        "number of anatomical enitites of type lateral structure phenotype",
                        "anatomical collection",
                        "developing mesenchymal condensation phenotype",
                        "digit plus metapodial segment",
                        "mandibular prominence",
                        "endoderm-derived structure",
                        "lower respiratory tract",
                        "absent anatomical entity",
                        "mandible",
                        "absent skeletal element in the limb",
                        "bone of lower jaw",
                        "pharyngeal arch 1",
                        "blood island phenotype",
                        "multicellular organism morphology phenotype",
                        "digestive system phenotype",
                        "digestive system element",
                        "protuberance",
                        "subdivision of tube",
                        "Esophageal atresia",
                        "decreased size of the anatomical entity",
                        "ventricular system of central nervous system",
                        "paired limb/fin segment",
                        "decreased rate of behavior process",
                        "skeleton phenotype",
                        "Orofacial cleft",
                        "number of anatomical enitites of type organ phenotype",
                        "Abnormality of mental function",
                        "absent anatomical entity in the forelimb",
                        "forebrain",
                        "upper digestive tract",
                        "Abnormality of metabolism/homeostasis",
                        "pectoral appendage bud",
                        "Aplasia/Hypoplasia affecting the eye",
                        "behavior process",
                        "central nervous system phenotype",
                        "sensory system phenotype",
                        "future central nervous system phenotype",
                        "cranial skeletal system phenotype",
                        "tube",
                        "digitopodium region",
                        "Absent radius",
                        "absent bone of appendage girdle complex",
                        "decreased qualitatively developmental process",
                        "eyelid phenotype",
                        "facial bone phenotype",
                        "cervical vertebra endochondral element",
                        "Micrognathia",
                        "Anotia",
                        "absent material anatomical entity in the skeletal system",
                        "homeostatic process",
                        "dense mesenchyme tissue",
                        "proximo-distal subdivision of respiratory tract",
                        "intramembranous bone phenotype",
                        "neurogenesis",
                        "absent multicellular anatomical structure in the reproductive system",
                        "Abnormal location of ears",
                        "Abnormal palate morphology",
                        "Decreased external ear position",
                        "biological_process in nervous system phenotype",
                        "Talipes",
                        "subdivision of skeletal system",
                        "endoderm phenotype",
                        "dermatocranium",
                        "mesenchyme phenotype",
                        "increased number of ventricle of nervous system",
                        "head bone",
                        "embryonic facial prominence",
                        "behavior",
                        "alimentary part of gastrointestinal system atresia",
                        "anatomical cavity",
                        "attention behavior",
                        "Attention deficit hyperactivity disorder",
                        "absent material anatomical entity in the limb bud",
                        "material entity",
                        "respiratory airway",
                        "Short attention span",
                        "nervous system process",
                        "Abnormal nervous system physiology",
                        "Abnormal volitional state",
                        "posterior neural tube",
                        "social behavior",
                        "cognition",
                        "Morphological central nervous system abnormality",
                        "male organism",
                        "cognitive behavior",
                        "decreased multicellular organismal process",
                        "absent anatomical entity in the head",
                        "anatomical structure physiology phenotype",
                        "anatomical system physiology phenotype",
                        "cardiovascular system phenotype",
                        "Recurrent maladaptive behavior",
                        "axon ensheathment in central nervous system phenotype",
                        "germ layer / neural crest",
                        "embryo morphology phenotype",
                        "decreased social inhibition",
                        "decreased biological_process",
                        "decreased behavior",
                        "multicellular organismal process",
                        "oligodendrocyte differentiation",
                        "closing of the organ part",
                        "hindbrain",
                        "Cognitive impairment",
                        "Reduced attention regulation",
                        "nervous system physiology phenotype",
                        "forebrain phenotype",
                        "Abnormality of the nervous system",
                        "circulatory system",
                        "hindbrain morphology phenotype",
                        "nervous system phenotype",
                        "increased width of material anatomical entity",
                        "proximo-distal subdivision of respiratory tract phenotype",
                        "material anatomical entity physiology phenotype",
                        "abdominal segment bone",
                        "biological_process phenotype",
                        "oral cavity",
                        "Growth delay",
                        "Abnormality of the skin",
                        "subdivision of organism along appendicular axis phenotype",
                        "growth",
                        "delayed biological_process",
                        "female reproductive organ morphology phenotype",
                        "growth phenotype",
                        "developmental process rate phenotype",
                        "Growth abnormality",
                        "developmental process phenotype",
                        "digit",
                        "development of anatomical entity phenotype",
                        "Abnormality of the integument",
                        "anatomical structure development",
                        "Aplasia/hypoplasia involving the skeleton",
                        "thoracic cavity element phenotype",
                        "multicellular organism development",
                        "neural fold morphology phenotype",
                        "Intrauterine growth retardation",
                        "decreased anatomical structure development",
                        "multi-limb segment region",
                        "developmental process",
                        "biological regulation phenotype",
                        "decreased qualitatively multicellular organism development",
                        "nasal bridge",
                        "absent anatomical structure in the ear",
                        "absent trunk region element in the multicellular organism",
                        "absent bone of appendage girdle complex in the limb",
                        "decreased embryo development",
                        "fused sacrum phenotype",
                        "anatomical structure development phenotype",
                        "decreased multicellular organism development",
                        "decreased qualitatively anatomical structure development",
                        "taxon specific phenotype",
                        "epithelial vesicle phenotype",
                        "digit 1 or 5 phenotype",
                        "unilaminar epithelium",
                        "somite phenotype",
                        "Aplasia/Hypoplasia of fingers",
                        "optic cup",
                        "absent abdomen element in the renal system",
                        "number of anatomical enitites of type anatomical structure phenotype",
                        "embryo development phenotype",
                        "digit 1 phenotype",
                        "absent organ in the forelimb",
                        "autopodial extension phenotype",
                        "autopodial skeleton",
                        "macromolecule biosynthetic process phenotype",
                        "manual digit phenotype",
                        "anatomical entity morphology in the manus phenotype",
                        "Finger aplasia",
                        "embryonic autopod plate",
                        "Abnormal eye morphology",
                        "absent organism subdivision",
                        "paired limb/fin segment phenotype",
                        "aplasia or hypoplasia of manual digit",
                        "mouth morphology phenotype",
                        "pelvic region of trunk",
                        "ocular adnexa phenotype",
                        "pharyngeal arch morphology phenotype",
                        "absent digit",
                        "manual digit 1",
                        "absent multicellular anatomical structure in the tissue",
                        "blood phenotype",
                        "segment of manus",
                        "acropodium region",
                        "mesoderm",
                        "neural tube",
                        "subdivision of organism along appendicular axis",
                        "regulation of metabolic process",
                        "manual digitopodium region",
                        "manual digit 1 morphology phenotype",
                        "delayed growth",
                        "absent organism subdivision in the multicellular organism",
                        "Abnormality of the hand",
                        "aplastic manual digit 1",
                        "manual digit plus metapodial segment",
                        "incomplete closing of the neural crest-derived structure",
                        "absent subdivision of head in the head",
                        "absent anatomical structure in the head",
                        "increased width of anatomical entity",
                        "dermal skeleton",
                        "alimentary part of gastrointestinal system",
                        "absent organism subdivision in the head",
                        "disconnected anatomical group",
                        "Aplasia/Hypoplasia of the external ear",
                        "aplasia or hypoplasia of ear",
                        "midface morphology phenotype",
                        "manus phenotype",
                        "Aplasia/Hypoplasia of the ear",
                        "absent multicellular anatomical structure in the head",
                        "absent subdivision of head",
                        "structure with developmental contribution from neural crest",
                        "absent material anatomical entity in the head",
                        "musculature",
                        "mesoderm morphology phenotype",
                        "craniocervical region morphology phenotype",
                        "brain ventricle phenotype",
                        "absent cavitated compound organ",
                        "absent external ear",
                        "uterus",
                        "Abnormal tracheal morphology",
                        "aplasia or hypoplasia of external ear",
                        "anatomical entity morphology in the appendage girdle complex phenotype",
                        "abdominal segment element phenotype",
                        "Delayed myelination",
                        "presomitic mesoderm",
                        "external ectoderm",
                        "vertebral column phenotype",
                        "paraxial mesoderm",
                        "pelvic region element phenotype",
                        "biological_process rate phenotype",
                        "dorsal region element",
                        "Hypoplastic sacrum",
                        "trunk region element",
                        "fused sacrum hypoplasia",
                        "pelvic complex",
                        "esophagus atresia",
                        "cell condensation",
                        "pelvic region element",
                        "multicellular anatomical structure atresia",
                        "midface phenotype",
                        "anatomical cluster",
                        "Aplasia/Hypoplasia involving the vertebral column",
                        "epithelial vesicle",
                        "incomplete closing of the multicellular anatomical structure",
                        "trunk mesenchyme",
                        "regulation of biosynthetic process",
                        "bone of dorsum phenotype",
                        "unilaminar epithelium phenotype",
                        "Abnormality of globe location",
                        "digestive system element phenotype",
                        "irregular bone",
                        "brain morphology phenotype",
                        "excretory system",
                        "Abnormal foot morphology",
                        "fused sacrum",
                        "trunk bone phenotype",
                        "number of anatomical enitites of type ectoderm-derived structure phenotype",
                        "aplasia or hypoplasia of vertebral column",
                        "renal/urinary system phenotype",
                        "foregut epithelium phenotype",
                        "presumptive paraxial mesoderm",
                        "closing of the material anatomical entity",
                        "migrating mesenchyme population phenotype",
                        "Abnormal skin morphology",
                        "presomitic mesoderm phenotype",
                        "Abnormal neck morphology",
                        "postcranial axial skeleton phenotype",
                        "increased number of ventricle of nervous system in the cerebrospinal fluid",
                        "Abnormality of the vertebral column",
                        "subdivision of trunk phenotype",
                        "trunk region element phenotype",
                        "penis",
                        "absent anatomical structure in the reproductive system",
                        "negative regulation of gene expression phenotype",
                        "manual digit morphology in the manus phenotype",
                        "vasculature of organ",
                        "Abnormal axial skeleton morphology",
                        "sclerotome phenotype",
                        "obsolete cell",
                        "brain phenotype",
                        "zone of organ",
                        "subdivision of vertebral column",
                        "aplasia or hypoplasia of fused sacrum",
                        "bone of jaw phenotype",
                        "entire embryonic mesenchyme",
                        "abdominal segment element",
                        "trunk bone",
                        "sacral region of vertebral column phenotype",
                        "viscus",
                        "compound organ",
                        "primordium",
                        "abdominal segment bone phenotype",
                        "alimentary part of gastrointestinal system phenotype",
                        "trunk",
                        "uterus phenotype",
                        "external male genitalia phenotype",
                        "absent subdivision of tube in the female reproductive system",
                        "cerebellum hypoplasia",
                        "Abnormal internal genitalia",
                        "closing of the ectoderm-derived structure",
                        "female reproductive organ phenotype",
                        "oviduct phenotype",
                        "facial skeleton",
                        "organ atresia",
                        "internal female genitalia morphology phenotype",
                        "anatomical wall phenotype",
                        "presumptive paraxial mesoderm phenotype",
                        "absent material anatomical entity in the female reproductive system",
                        "closing of the anatomical structure",
                        "Abnormal reproductive system morphology",
                        "reproductive structure",
                        "Abnormal morphology of female internal genitalia",
                        "Abnormality of the uterus",
                        "telencephalon",
                        "absent subdivision of tube",
                        "number of anatomical enitites of type subdivision of tube phenotype",
                        "orifice atresia",
                        "oviduct",
                        "endochondral element phenotype",
                        "absent anatomical entity in the reproductive system",
                        "root",
                        "absent subdivision of oviduct",
                        "esophagus morphology phenotype",
                        "female reproductive system",
                        "incomplete closing of the material anatomical entity",
                        "reproductive system morphology phenotype",
                        "absent bone element in the limb",
                        "number of anatomical enitites of type organ part phenotype",
                        "increased number of material anatomical entity in the cerebrospinal fluid",
                        "female organism",
                        "absent subdivision of oviduct in the female reproductive system",
                        "absent organ part",
                        "Aplasia/Hypoplasia of the mandible",
                        "aplasia or hypoplasia of uterus",
                        "female organism phenotype",
                        "anatomical conduit phenotype",
                        "absent organ part in the female reproductive system",
                        "female reproductive system phenotype",
                        "absent anatomical entity in the ear",
                        "Abnormality of the genitourinary system",
                        "subdivision of oviduct",
                        "absent long bone",
                        "Abnormality of the musculoskeletal system",
                        "Abnormality of the genital system",
                        "Abnormal morphology of the radius",
                        "reproductive organ phenotype",
                        "increased width of ectoderm-derived structure",
                        "Aplasia/hypoplasia of the uterus",
                        "subdivision of oviduct phenotype",
                        "reproductive structure phenotype",
                        "forelimb long bone phenotype",
                        "female reproductive organ",
                        "internal genitalia",
                        "metencephalon phenotype",
                        "leg",
                        "Global developmental delay",
                        "organ subunit",
                        "Neurodevelopmental delay",
                        "negative regulation of metabolic process",
                        "regulation of macromolecule metabolic process",
                        "bone of pectoral complex phenotype",
                        "metabolic process",
                        "primordium phenotype",
                        "musculature of body phenotype",
                        "negative regulation of macromolecule metabolic process",
                        "negative regulation of biosynthetic process",
                        "oral cavity morphology phenotype",
                        "biosynthetic process phenotype",
                        "trunk phenotype",
                        "biological regulation",
                        "cell phenotype",
                        "anatomical entity atresia",
                        "macromolecule metabolic process",
                        "biosynthetic process",
                        "pectoral appendage bud phenotype",
                        "closing of the anatomical system",
                        "negative regulation of biological process",
                        "Abnormal oral morphology",
                        "regulation of cellular process",
                        "gene expression phenotype",
                        "Abnormal cellular physiology",
                        "camera-type eye phenotype",
                        "increased number of anatomical entity in the cerebrospinal fluid",
                        "Abnormal cellular phenotype",
                        "cellular process phenotype",
                        "cellular process",
                        "external soft tissue zone phenotype",
                        "negative regulation of macromolecule biosynthetic process",
                        "homeostatic process phenotype",
                        "Chromosomal breakage induced by crosslinking agents",
                        "closing of the subdivision of digestive tract",
                        "closing of the multicellular anatomical structure",
                        "viscus phenotype",
                        "cerebrospinal fluid",
                        "pharyngeal arch system",
                        "material anatomical entity atresia",
                        "Hypoplastic male external genitalia",
                        "Aplasia/hypoplasia involving bones of the hand",
                        "closing of the subdivision of tube",
                        "absent multicellular anatomical structure in the ear",
                        "Abnormal esophagus morphology",
                        "skeletal system phenotype",
                        "Abnormality of the gastrointestinal tract",
                        "Aplasia of the uterus",
                        "trunk region element atresia",
                        "Hypertelorism",
                        "Feeding difficulties",
                        "closing of the trunk region element",
                        "esophagus",
                        "Abnormal digestive system morphology",
                        "subdivision of digestive tract atresia",
                        "chordal neural plate",
                        "bone of craniocervical region phenotype",
                        "Abnormal hindbrain morphology",
                        "Abnormal nervous system morphology",
                        "absent forelimb endochondral element in the limb",
                        "neural tube phenotype",
                        "epithelial tube phenotype",
                        "epithelial tube",
                        "external ectoderm morphology phenotype",
                        "metencephalon",
                        "central nervous system morphology phenotype",
                        "nervous system development",
                        "anatomical line phenotype",
                        "Abnormal metencephalon morphology",
                        "nervous system morphology phenotype",
                        "segmental subdivision of nervous system",
                        "oral cavity phenotype",
                        "Positional foot deformity",
                        "segmental subdivision of nervous system phenotype",
                        "Atypical behavior",
                        "regional part of nervous system",
                        "nose tip",
                        "posterior neural tube phenotype",
                        "eye primordium phenotype",
                        "aplasia or hypoplasia of manual digit 1",
                        "cerebellum",
                        "thoracic segment organ",
                        "segmental subdivision of hindbrain",
                        "central nervous system",
                        "Aplasia/Hypoplasia of the thumb",
                        "regional part of brain",
                        "absent endochondral element in the limb",
                        "absent bone of appendage girdle complex in the forelimb",
                        "segmental subdivision of hindbrain phenotype",
                        "absent anatomical structure in the female reproductive system",
                        "Gastrointestinal atresia",
                        "cerebellum phenotype",
                        "upper jaw region",
                        "brain ventricle/choroid plexus phenotype",
                        "midface",
                        "Abnormality of the face",
                        "anatomical space phenotype",
                        "subdivision of skeletal system phenotype",
                        "incomplete closing of the anatomical entity",
                        "anatomical space",
                        "male reproductive system phenotype",
                        "secondary palate",
                        "increased number of anatomical structure in the cerebrospinal fluid",
                        "incomplete closing of the anatomical structure",
                        "roof of mouth",
                        "mesenchyme",
                        "incomplete closing of the secondary palate",
                        "endochondral bone phenotype",
                        "autopod region",
                        "Abnormality of the mouth",
                        "number of anatomical enitites of type abdomen element phenotype",
                        "incomplete closing of the structure with developmental contribution from neural crest",
                        "immaterial entity",
                        "Craniofacial cleft",
                        "Cleft palate",
                        "vertebral column",
                        "Abnormal oral cavity morphology",
                        "anatomical cavity phenotype",
                        "Aplasia/Hypoplasia of the sacrum",
                        "External genital hypoplasia",
                        "penis hypoplasia",
                        "thoracic segment of trunk",
                        "male reproductive system",
                        "external male genitalia hypoplasia",
                        "Abnormality of the orbital region",
                        "paraxial mesoderm phenotype",
                        "external genitalia phenotype",
                        "penis phenotype",
                        "male reproductive organ",
                        "external genitalia",
                        "aplasia or hypoplasia of cerebellum",
                        "foregut epithelium",
                        "endoderm morphology phenotype",
                        "endoderm-derived structure phenotype",
                        "digestive tract epithelium",
                        "digestive tract epithelium phenotype",
                        "Wide nasal bridge",
                        "male organism phenotype",
                        "endoderm of foregut phenotype",
                        "internal female genitalia",
                        "cerebrospinal fluid morphology phenotype",
                        "presumptive structure",
                        "endoderm of foregut",
                        "tracheobronchial tree morphology phenotype",
                        "size of anatomical entity phenotype",
                        "endoderm",
                        "ectoderm phenotype",
                        "respiratory tube",
                        "multicellular anatomical structure phenotype",
                        "number of anatomical enitites of type reproductive structure phenotype",
                        "increased number of organ part",
                        "Chromosome breakage",
                        "endo-epithelium phenotype",
                        "pre-chordal neural plate phenotype",
                        "behavior phenotype",
                        "Metazoa",
                        "anterior neural tube phenotype",
                        "closing of the organ",
                        "organism substance",
                        "head",
                        "transudate",
                        "Abnormal cerebral ventricle morphology",
                        "hemolymphoid system",
                        "cerebrospinal fluid phenotype",
                        "location of eyeball of camera-type eye phenotype",
                        "brain ventricle/choroid plexus",
                        "vasculature of central nervous system plus retina",
                        "vascular plexus",
                        "bone of dorsum",
                        "brain ventricle/choroid plexus morphology phenotype",
                        "thoracic segment organ phenotype",
                        "increased number of multicellular anatomical structure in the cerebrospinal fluid",
                        "blood island",
                        "multicellular organism development phenotype",
                        "incomplete closing of the roof of mouth",
                        "brain",
                        "increased number of anatomical entity in the blood",
                        "hematopoietic system phenotype",
                        "Abnormal skull morphology",
                        "increased number of brain ventricle/choroid plexus",
                        "increased number of anatomical structure",
                        "increased number of ectoderm-derived structure",
                        "respiratory tract",
                        "brain ventricle morphology phenotype",
                        "Abnormal brain morphology",
                        "cardiovascular system",
                        "increased number of anatomical entity",
                        "vasculature",
                        "zeugopodial skeleton",
                        "number of anatomical entities of type anatomical entity in blood phenotype",
                    ],
                    "highlighting": None,
                },
                {
                    "id": "MONDO:0010953",
                    "category": "biolink:Disease",
                    "name": "Fanconi anemia complementation group E",
                    "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.",
                    "provided_by": "phenio_nodes",
                    "xref": [
                        "DOID:0111084",
                        "GARD:15324",
                        "MEDGEN:463628",
                        "NCIT:C125709",
                        "OMIM:600901",
                        "UMLS:C3160739",
                    ],
                    "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",
                    ],
                    "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"],
                    "subsets": ["clingen", "gard_rare", "nord_rare", "otar", "rare"],
                    "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",
                    ],
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                        "CL:0000094",
                        "UPHENO:0002880",
                        "UPHENO:0025545",
                        "UPHENO:0003799",
                        "UBERON:0034925",
                        "UBERON:0000467",
                        "UPHENO:0005092",
                        "UBERON:0004288",
                        "GO:0009987",
                        "HP:0005561",
                        "UBERON:0005291",
                        "UBERON:0003104",
                        "HP:0011354",
                        "UPHENO:0069605",
                        "UBERON:0000153",
                        "UBERON:0010363",
                        "UPHENO:0025811",
                        "HP:0000081",
                        "UPHENO:0008487",
                        "UPHENO:0053610",
                        "HP:0011842",
                        "UPHENO:0002352",
                        "UPHENO:0087665",
                        "UPHENO:0025955",
                        "UPHENO:0076754",
                        "CL:0000232",
                        "UPHENO:0080187",
                        "UPHENO:0009010",
                        "UPHENO:0026023",
                        "UBERON:5006048",
                        "UPHENO:0027631",
                        "HP:0040072",
                        "UBERON:0011676",
                        "UBERON:0001434",
                        "UPHENO:0004466",
                        "UPHENO:0069327",
                        "UPHENO:0011573",
                        "UPHENO:0088186",
                        "UBERON:0000923",
                        "UPHENO:0049588",
                        "HP:0000119",
                        "UBERON:0002101",
                        "UBERON:0001440",
                        "UPHENO:0009295",
                        "HP:0009997",
                        "HP:0002715",
                        "UPHENO:0026757",
                        "UPHENO:0075902",
                        "UPHENO:0076727",
                        "UPHENO:0002751",
                        "HP:0000924",
                        "UPHENO:0053612",
                        "UPHENO:0003163",
                        "UPHENO:0003811",
                        "UPHENO:0009344",
                        "NBO:0000313",
                        "UPHENO:0002940",
                        "UBERON:0010316",
                        "UPHENO:0086546",
                        "UPHENO:0025585",
                        "UBERON:0003081",
                        "UPHENO:0026504",
                        "UBERON:0010707",
                        "UBERON:0010712",
                        "BFO:0000002",
                        "UPHENO:0025508",
                        "UBERON:0005419",
                        "UBERON:0002495",
                        "HP:0000135",
                        "UBERON:0002529",
                        "GO:0010605",
                        "UBERON:0015061",
                        "UPHENO:0085302",
                        "UBERON:0011584",
                        "UPHENO:0076703",
                        "UPHENO:0003812",
                        "UPHENO:0025882",
                        "UPHENO:0002564",
                        "HP:0011875",
                        "UBERON:0015025",
                        "UPHENO:0088123",
                        "UBERON:0005423",
                        "UBERON:0000075",
                        "UPHENO:0002785",
                        "UPHENO:0026640",
                        "UPHENO:0026312",
                        "HP:0000953",
                        "UPHENO:0008430",
                        "UPHENO:0003020",
                        "UBERON:0010912",
                        "HP:0012759",
                        "HP:0006501",
                        "UPHENO:0080010",
                        "UPHENO:0026073",
                        "UPHENO:0003116",
                        "HP:0011355",
                        "UPHENO:0012440",
                        "UPHENO:0011548",
                        "HP:0033127",
                        "HP:0012210",
                        "UBERON:0006598",
                        "UPHENO:0002747",
                        "UPHENO:0006894",
                        "UPHENO:0026095",
                        "UPHENO:0075219",
                        "UBERON:0002102",
                        "UBERON:0005881",
                        "UPHENO:0025547",
                        "UBERON:0004111",
                        "UPHENO:0002542",
                        "UPHENO:0046741",
                        "UPHENO:0011559",
                        "UPHENO:0011566",
                        "UPHENO:0003366",
                        "UPHENO:0005517",
                        "HP:0009115",
                        "GO:0010556",
                        "UBERON:0007272",
                        "UPHENO:0010808",
                        "HP:0012372",
                        "UPHENO:0026097",
                        "HP:0003953",
                        "UPHENO:0027547",
                        "UBERON:0015410",
                        "UPHENO:0027017",
                        "UPHENO:0009163",
                        "UPHENO:0008475",
                        "UPHENO:0002903",
                        "UPHENO:0087661",
                        "UBERON:0019221",
                        "UPHENO:0002650",
                        "UPHENO:0026643",
                        "NBO:0000001",
                        "UPHENO:0005030",
                        "UPHENO:0004909",
                        "UBERON:0013701",
                        "UBERON:0008962",
                        "HP:0001933",
                        "UPHENO:0076723",
                        "HP:0010461",
                        "HP:0002973",
                        "UBERON:0003607",
                        "UPHENO:0004900",
                        "HP:0003254",
                        "UPHENO:0050625",
                        "UPHENO:0002323",
                        "UPHENO:0080209",
                        "UPHENO:0026239",
                        "HP:0009121",
                        "UPHENO:0026813",
                        "HP:0004323",
                        "UPHENO:0002861",
                        "UBERON:0003460",
                        "UPHENO:0026344",
                        "UPHENO:0008865",
                        "UPHENO:0002816",
                        "UBERON:0001017",
                        "UPHENO:0003514",
                        "UPHENO:0087363",
                        "UPHENO:0025852",
                        "UPHENO:0004433",
                        "HP:0045060",
                        "UPHENO:0002659",
                        "UPHENO:0004360",
                        "UPHENO:0004827",
                        "UPHENO:0025845",
                        "NCBITaxon:6072",
                        "UPHENO:0069523",
                        "UPHENO:0081511",
                        "HP:0001249",
                        "UPHENO:0002600",
                        "UPHENO:0004680",
                        "UPHENO:0026074",
                        "UPHENO:0002593",
                        "HP:0011873",
                        "HP:0003213",
                        "UPHENO:0003412",
                        "HP:0001155",
                        "UBERON:0001423",
                        "UPHENO:0066927",
                        "UBERON:0003466",
                        "HP:0001627",
                        "UPHENO:0087907",
                        "UPHENO:0008703",
                        "UPHENO:0082875",
                        "CL:0000329",
                        "UPHENO:0076740",
                        "NCBITaxon:1",
                        "UPHENO:0008743",
                        "UPHENO:0087849",
                        "UPHENO:0003432",
                        "UPHENO:0002541",
                        "HP:0003974",
                        "CL:0002242",
                        "UPHENO:0025587",
                        "UPHENO:0079876",
                        "UBERON:0004734",
                        "UPHENO:0011492",
                        "UBERON:0000489",
                        "UBERON:0010538",
                        "UBERON:0001463",
                        "UPHENO:0050620",
                        "UPHENO:0086002",
                        "UBERON:0002428",
                        "HP:0001875",
                        "UBERON:0003606",
                        "UBERON:0002471",
                        "UPHENO:0086769",
                        "UPHENO:0003159",
                        "UBERON:0015021",
                        "UPHENO:0026486",
                        "UBERON:0010703",
                        "UPHENO:0003227",
                        "HP:0005927",
                        "UPHENO:0004173",
                        "UBERON:0004456",
                        "UPHENO:0002526",
                        "UPHENO:0002964",
                        "UPHENO:0002632",
                        "UPHENO:0046740",
                        "UPHENO:0003413",
                        "UPHENO:0002969",
                        "HP:0001909",
                        "UPHENO:0004475",
                        "UPHENO:0005016",
                        "UPHENO:0012274",
                        "UBERON:0012358",
                        "UPHENO:0079872",
                        "UPHENO:0025546",
                        "UBERON:0004128",
                        "UPHENO:0026096",
                        "UPHENO:0026078",
                        "UPHENO:0003065",
                        "GO:0009058",
                        "UBERON:0003102",
                        "UPHENO:0011568",
                        "UBERON:0000079",
                        "UPHENO:0027231",
                        "UPHENO:0079828",
                        "HP:0000478",
                        "UPHENO:0086635",
                        "HP:0100542",
                        "UPHENO:0002750",
                        "UPHENO:0002571",
                        "UPHENO:0003005",
                        "RO:0002577",
                        "UPHENO:0052178",
                        "UBERON:0002389",
                        "HP:0009778",
                        "UPHENO:0009341",
                        "UPHENO:0085263",
                        "UPHENO:0025211",
                        "UPHENO:0076724",
                        "UPHENO:0008709",
                        "UBERON:0000073",
                        "UPHENO:0002594",
                        "GO:0048523",
                        "UPHENO:0025507",
                        "UPHENO:0009391",
                        "UPHENO:0002896",
                        "GO:0009890",
                        "UBERON:0011216",
                        "UBERON:0004347",
                        "UPHENO:0002719",
                        "HP:0009381",
                        "UBERON:0011582",
                        "UBERON:0005417",
                        "HP:0001872",
                        "UPHENO:0088166",
                        "HP:0009815",
                        "UBERON:0001015",
                        "HP:0001873",
                        "UPHENO:0050106",
                        "UPHENO:0066913",
                        "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",
                    ],
                    "highlighting": None,
                },
                {
                    "id": "MONDO:0001083",
                    "category": "biolink:Disease",
                    "name": "Fanconi renotubular syndrome",
                    "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.",
                    "provided_by": "phenio_nodes",
                    "xref": [
                        "DOID:1062",
                        "GARD:9120",
                        "MEDGEN:4653",
                        "MESH:D005198",
                        "NANDO:2100027",
                        "NANDO:2200187",
                        "NCIT:C3034",
                        "SCTID:236466005",
                        "SCTID:40488004",
                        "UMLS:C0015624",
                    ],
                    "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",
                    ],
                    "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"],
                    "subsets": ["gard_rare", "nord_rare", "otar", "rare"],
                    "namespace": "MONDO",
                    "has_phenotype_count": 0,
                    "highlighting": None,
                },
                {
                    "id": "MONDO:0019391",
                    "category": "biolink:Disease",
                    "name": "Fanconi anemia",
                    "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.",
                    "provided_by": "phenio_nodes",
                    "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",
                    ],
                    "synonym": [
                        "Fanconi anemia",
                        "Fanconi pancytopenia",
                        "Fanconi panmyelopathy",
                        "Fanconi's anaemia",
                        "Fanconi's anemia",
                        "Panmyelopathy, Fanconi",
                        "pancytopenia, congenital",
                        "primary erythroid hypoplasia",
                    ],
                    "exact_synonyms": [
                        "Fanconi anemia|Fanconi pancytopenia|Fanconi panmyelopathy|Fanconi's anaemia|Fanconi's anemia|Panmyelopathy, Fanconi|pancytopenia, congenital|primary erythroid hypoplasia"
                    ],
                    "subsets": [
                        "clingen",
                        "gard_rare",
                        "nord_rare",
                        "ordo_disorder",
                        "ordo_malformation_syndrome",
                        "orphanet_rare",
                        "otar",
                        "rare",
                    ],
                    "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_count": 106,
                    "has_phenotype_closure": [
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                        "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",
                    ],
                    "highlighting": None,
                },
                {
                    "id": "MONDO:0013248",
                    "category": "biolink:Disease",
                    "name": "Fanconi anemia complementation group O",
                    "description": "Any Fanconi anemia in which the cause of the disease is a mutation in the RAD51C gene.",
                    "provided_by": "phenio_nodes",
                    "xref": ["DOID:0111096", "GARD:15656", "MEDGEN:462003", "OMIM:613390", "UMLS:C3150653"],
                    "synonym": [
                        "FANCO",
                        "Fanconi Anemia, complementation group type O",
                        "Fanconi anaemia caused by mutation in RAD51C",
                        "Fanconi anaemia caused by mutation in Rad51C",
                        "Fanconi anaemia complementation group type O",
                        "Fanconi anemia caused by mutation in RAD51C",
                        "Fanconi anemia caused by mutation in Rad51C",
                        "Fanconi anemia complementation group type O",
                        "Fanconi anemia, complementation group O",
                        "RAD51C Fanconi anaemia",
                        "RAD51C Fanconi anemia",
                        "Rad51C Fanconi anaemia",
                        "Rad51C Fanconi anemia",
                    ],
                    "exact_synonyms": [
                        "FANCO|Fanconi Anemia, complementation group type O|Fanconi anaemia caused by mutation in RAD51C|Fanconi anaemia caused by mutation in Rad51C|Fanconi anaemia complementation group type O|Fanconi anemia caused by mutation in RAD51C|Fanconi anemia caused by mutation in Rad51C|Fanconi anemia complementation group type O|RAD51C Fanconi anaemia|RAD51C Fanconi anemia|Rad51C Fanconi anaemia|Rad51C Fanconi anemia"
                    ],
                    "related_synonyms": ["Fanconi anemia, complementation group O"],
                    "subsets": ["gard_rare", "nord_rare", "rare"],
                    "namespace": "MONDO",
                    "has_phenotype": [
                        "HP:0000126",
                        "HP:0002984",
                        "HP:0000028",
                        "HP:0009778",
                        "HP:0009623",
                        "HP:0009777",
                        "HP:0001627",
                        "HP:0000107",
                        "HP:0040012",
                        "HP:0003241",
                        "HP:0004322",
                        "HP:0001245",
                        "HP:0002023",
                        "HP:0003774",
                        "HP:0025023",
                    ],
                    "has_phenotype_label": [
                        "Hydronephrosis",
                        "Hypoplasia of the radius",
                        "Cryptorchidism",
                        "Short thumb",
                        "Proximal placement of thumb",
                        "Absent thumb",
                        "Abnormal heart morphology",
                        "Renal cyst",
                        "Chromosome breakage",
                        "External genital hypoplasia",
                        "Short stature",
                        "Small thenar eminence",
                        "Anal atresia",
                        "Stage 5 chronic kidney disease",
                        "Rectal atresia",
                    ],
                    "has_phenotype_count": 15,
                    "has_phenotype_closure": [
                        "UBERON:0000160",
                        "UBERON:0001046",
                        "UBERON:0006866",
                        "HP:0011024",
                        "UBERON:0013522",
                        "UBERON:0000481",
                        "NCBITaxon:131567",
                        "HP:0002242",
                        "NCBITaxon:6072",
                        "NCBITaxon:33208",
                        "HP:0002589",
                        "HP:0025023",
                        "UPHENO:0002994",
                        "UPHENO:0087367",
                        "UPHENO:0063632",
                        "NCBITaxon:1",
                        "UPHENO:0084771",
                        "UPHENO:0076773",
                        "HP:0012732",
                        "UPHENO:0002988",
                        "UBERON:0004921",
                        "UPHENO:0063575",
                        "UPHENO:0002546",
                        "UBERON:0004907",
                        "UPHENO:0074330",
                        "UBERON:0013765",
                        "UPHENO:0063586",
                        "UPHENO:0063563",
                        "UPHENO:0002714",
                        "UPHENO:0004518",
                        "HP:0011100",
                        "HP:0002034",
                        "UPHENO:0002246",
                        "UPHENO:0074311",
                        "UPHENO:0002377",
                        "UPHENO:0002385",
                        "UPHENO:0002308",
                        "UPHENO:0002442",
                        "UPHENO:0002386",
                        "UPHENO:0002360",
                        "UPHENO:0002267",
                        "UPHENO:0002269",
                        "UPHENO:0002422",
                        "HP:0011277",
                        "HP:0000083",
                        "UPHENO:0002812",
                        "UPHENO:0002859",
                        "UPHENO:0002548",
                        "UPHENO:0086644",
                        "HP:0004378",
                        "UPHENO:0074237",
                        "UPHENO:0074229",
                        "HP:0002023",
                        "UPHENO:0063599",
                        "UBERON:0000025",
                        "UBERON:0001245",
                        "UPHENO:0063596",
                        "UPHENO:0002426",
                        "UPHENO:0074230",
                        "UPHENO:0076803",
                        "UPHENO:0063577",
                        "UBERON:0001007",
                        "HP:0025031",
                        "UPHENO:0074228",
                        "UPHENO:0063562",
                        "UPHENO:0063594",
                        "UPHENO:0002833",
                        "UPHENO:0002839",
                        "UBERON:0001555",
                        "UPHENO:0074227",
                        "UBERON:0001630",
                        "UPHENO:0002647",
                        "UPHENO:0002725",
                        "HP:0002250",
                        "UPHENO:0003022",
                        "UBERON:0007269",
                        "UPHENO:0002651",
                        "UBERON:0004481",
                        "UPHENO:0002786",
                        "HP:0001446",
                        "UBERON:0000059",
                        "UBERON:0004489",
                        "UPHENO:0002649",
                        "UBERON:0014793",
                        "UBERON:0004121",
                        "UBERON:0034929",
                        "HP:0012622",
                        "UPHENO:0003057",
                        "HP:0003011",
                        "UPHENO:0004487",
                        "UPHENO:0081341",
                        "UPHENO:0069254",
                        "HP:0001510",
                        "UPHENO:0000543",
                        "GO:0040007",
                        "UPHENO:0076735",
                        "UPHENO:0000541",
                        "UPHENO:0049874",
                        "HP:0012211",
                        "HP:0000002",
                        "HP:0003241",
                        "UPHENO:0050065",
                        "HP:0003220",
                        "UPHENO:0002861",
                        "UPHENO:0001360",
                        "UBERON:0003460",
                        "UPHENO:0074335",
                        "HP:0000028",
                        "UBERON:0002386",
                        "UBERON:0003103",
                        "UPHENO:0002648",
                        "UBERON:0004375",
                        "UPHENO:0078606",
                        "UPHENO:0026108",
                        "UBERON:0002204",
                        "UPHENO:0046397",
                        "UPHENO:0011536",
                        "UPHENO:0046445",
                        "HP:0040068",
                        "UPHENO:0003084",
                        "UBERON:0007271",
                        "GO:0008150",
                        "UPHENO:0002650",
                        "UBERON:0004357",
                        "UPHENO:0002655",
                        "HP:0009623",
                        "UBERON:0010712",
                        "UPHENO:0068921",
                        "UBERON:0010707",
                        "HP:0003026",
                        "HP:0000077",
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                        "UBERON:0002513",
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                        "UBERON:0010130",
                        "UPHENO:0009020",
                        "UBERON:0003102",
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                        "UBERON:5001463",
                        "UBERON:0019221",
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                        "UBERON:0007100",
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                        "UPHENO:0069236",
                        "UBERON:0005451",
                        "UBERON:0004708",
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                        "NCBITaxon:2759",
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                        "NCBITaxon:33154",
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                        "UBERON:0006058",
                        "MPATH:0",
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                        "UPHENO:0084841",
                        "UBERON:0015212",
                        "MPATH:55",
                        "MPATH:62",
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                        "HP:0040012",
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                        "UPHENO:0001303",
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                        "UBERON:0011216",
                        "UBERON:0004347",
                        "UPHENO:0002719",
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                        "HP:0001939",
                        "UPHENO:0003047",
                        "GO:0008152",
                        "UPHENO:0049873",
                        "GO:0043170",
                        "GO:0048519",
                        "UPHENO:0046505",
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                        "BFO:0000015",
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                        "UBERON:0012140",
                        "HP:0011017",
                        "GO:0009892",
                        "GO:0060255",
                        "HP:0025354",
                    ],
                    "has_phenotype_closure_label": [
                        "Eumetazoa",
                        "root",
                        "hindgut phenotype",
                        "large intestine",
                        "Anorectal anomaly",
                        "Abnormal rectum morphology",
                        "multi-tissue structure phenotype",
                        "Intestinal atresia",
                        "lower digestive tract",
                        "intestine",
                        "hindgut",
                        "terminal part of digestive tract",
                        "rectum",
                        "alimentary part of gastrointestinal system atresia",
                        "Abnormality of the gastrointestinal tract",
                        "subdivision of tube",
                        "rectum morphology phenotype",
                        "rectum phenotype",
                        "digestive system element phenotype",
                        "intestine phenotype",
                        "intestine morphology phenotype",
                        "Eukaryota",
                        "anal region",
                        "alimentary part of gastrointestinal system phenotype",
                        "Rectal atresia",
                        "alimentary part of gastrointestinal system morphology phenotype",
                        "subdivision of digestive tract phenotype",
                        "digestive system element",
                        "material anatomical entity physiology phenotype",
                        "Abnormality of the urinary system physiology",
                        "Abnormal renal physiology",
                        "Renal insufficiency",
                        "abdomen element physiology phenotype",
                        "multicellular anatomical structure physiology phenotype",
                        "lateral structure physiology phenotype",
                        "anatomical structure physiology phenotype",
                        "organ physiology phenotype",
                        "trunk region element physiology phenotype",
                        "compound organ physiology phenotype",
                        "renal system physiology phenotype",
                        "closing of the anatomical conduit",
                        "ectoderm-derived structure atresia",
                        "closing of the ectoderm-derived structure",
                        "closing of the material anatomical entity",
                        "anus morphology phenotype",
                        "Abnormality of the anus",
                        "anus",
                        "Chronic kidney disease",
                        "orifice",
                        "orifice atresia",
                        "tube phenotype",
                        "Anal atresia",
                        "anus atresia",
                        "ectoderm-derived structure",
                        "closing of the anatomical entity",
                        "material anatomical entity atresia",
                        "multicellular anatomical structure atresia",
                        "closing of the anatomical structure",
                        "closing of the multicellular anatomical structure",
                        "closing of the subdivision of tube",
                        "Abnormality of the musculature",
                        "Abnormality of the musculature of the hand",
                        "musculature of limb phenotype",
                        "musculature of manus phenotype",
                        "Abnormal skeletal muscle morphology",
                        "pectoral appendage musculature phenotype",
                        "thenar eminence phenotype",
                        "musculature of pectoral complex",
                        "musculature of manus",
                        "muscle organ phenotype",
                        "musculature of upper limb",
                        "palmar/plantar part of autopod",
                        "Abnormal intestine morphology",
                        "Small thenar eminence",
                        "muscle structure phenotype",
                        "palmar part of manus phenotype",
                        "musculature of pectoral complex phenotype",
                        "Abnormality of the thenar eminence",
                        "Abnormal digestive system morphology",
                        "Abnormality of the musculature of the upper limbs",
                        "musculature of limb",
                        "Abnormality of the digestive system",
                        "muscle structure",
                        "Growth abnormality",
                        "decreased size of the multicellular organism",
                        "growth phenotype",
                        "anatomical entity height phenotype",
                        "delayed biological_process",
                        "Short stature",
                        "growth",
                        "decreased height of the multicellular organism",
                        "Growth delay",
                        "External genital hypoplasia",
                        "digestive system",
                        "obsolete cell",
                        "programmed DNA elimination by chromosome breakage",
                        "forelimb endochondral element phenotype",
                        "Abnormal limb bone morphology",
                        "decreased length of digit 1 or 5",
                        "musculoskeletal system",
                        "decreased length of forelimb bone",
                        "zeugopod",
                        "anatomical system phenotype",
                        "bone of free limb or fin",
                        "bone of pectoral complex",
                        "dilated renal pelvis",
                        "decreased size of the manual digit",
                        "skeleton phenotype",
                        "musculature of body phenotype",
                        "delayed growth",
                        "digit 1",
                        "paired limb/fin segment",
                        "digit 1 phenotype",
                        "hindgut morphology phenotype",
                        "decreased size of the bone of pectoral complex",
                        "abdomen",
                        "anatomical entity morphology in the manus phenotype",
                        "pectoral complex",
                        "decreased length of bone element",
                        "biological regulation",
                        "anatomical collection",
                        "anatomical system physiology phenotype",
                        "cardiovascular system phenotype",
                        "radius bone hypoplasia",
                        "forelimb bone phenotype",
                        "musculature phenotype",
                        "forelimb bud morphology phenotype",
                        "negative regulation of cellular process",
                        "decreased size of the organ",
                        "Cryptorchidism",
                        "autopod region morphology phenotype",
                        "heart",
                        "appendage",
                        "bone of appendage girdle complex phenotype",
                        "paired limb/fin bud",
                        "limb endochondral element",
                        "anatomical entity morphology in the pectoral complex phenotype",
                        "external genitalia",
                        "Aplasia/hypoplasia involving the skeleton",
                        "reproductive system phenotype",
                        "limb bud phenotype",
                        "Abnormal gastrointestinal tract morphology",
                        "regulation of biological process",
                        "Abnormality of the skeletal system",
                        "long bone phenotype",
                        "anatomical structure phenotype",
                        "anatomical entity physiology phenotype",
                        "programmed DNA elimination by chromosome breakage phenotype",
                        "decreased length of anatomical structure",
                        "closing of the subdivision of digestive tract",
                        "decreased size of the multicellular anatomical structure in the pectoral complex",
                        "negative regulation of gene expression",
                        "Hypoplasia of the radius",
                        "muscle organ morphology phenotype",
                        "decreased length of manual digit 1 or 5",
                        "Forearm undergrowth",
                        "heart plus pericardium",
                        "decreased size of the forelimb endochondral element",
                        "Abnormality of limb bone",
                        "limb segment",
                        "subdivision of skeleton phenotype",
                        "zeugopodial skeleton",
                        "kidney",
                        "long bone",
                        "endochondral bone",
                        "decreased length of long bone",
                        "bone of appendage girdle complex",
                        "decreased size of the forelimb zeugopod bone",
                        "multi-tissue structure",
                        "thoracic segment organ",
                        "musculoskeletal system phenotype",
                        "organ system subdivision",
                        "aplasia or hypoplasia of anatomical entity",
                        "decreased length of endochondral bone",
                        "internal anal region",
                        "decreased size of the endochondral element",
                        "cellular process",
                        "Aplasia/Hypoplasia of the radius",
                        "germ layer / neural crest phenotype",
                        "negative regulation of biosynthetic process",
                        "limb bone morphology phenotype",
                        "anatomical structure atresia",
                        "limb bone",
                        "decreased length of limb endochondral element",
                        "absent anatomical structure in the forelimb",
                        "Abnormal anus morphology",
                        "appendage phenotype",
                        "autopodial extension phenotype",
                        "forelimb skeleton phenotype",
                        "Abnormal forearm morphology",
                        "system",
                        "limb bone phenotype",
                        "closing of the anatomical system",
                        "biosynthetic process",
                        "radius bone phenotype",
                        "male reproductive organ phenotype",
                        "musculature of upper limb phenotype",
                        "surface structure",
                        "decreased size of the skeletal element",
                        "bone of pectoral complex phenotype",
                        "Abnormal upper limb bone morphology",
                        "digit morphology phenotype",
                        "decreased size of the material anatomical entity in the pectoral complex",
                        "forelimb bud",
                        "limb skeleton subdivision phenotype",
                        "developmental and structural abnormality",
                        "decreased length of forelimb endochondral element",
                        "deviation of manual digit 1",
                        "Aplasia/hypoplasia involving bones of the upper limbs",
                        "appendicular skeleton phenotype",
                        "renal pelvis phenotype",
                        "bone of free limb or fin phenotype",
                        "paired limb/fin skeleton phenotype",
                        "decreased length of material anatomical entity",
                        "trunk region element phenotype",
                        "negative regulation of gene expression phenotype",
                        "skeletal system morphology phenotype",
                        "Short long bone",
                        "skeleton",
                        "cavitated compound organ physiology phenotype",
                        "skeletal element phenotype",
                        "presumptive structure phenotype",
                        "kidney morphology phenotype",
                        "Abnormal reproductive system morphology",
                        "subdivision of digestive tract",
                        "developing anatomical structure phenotype",
                        "pectoral appendage bud phenotype",
                        "multicellular organism height phenotype",
                        "All",
                        "pectoral appendage musculature",
                        "mesoderm phenotype",
                        "Opisthokonta",
                        "embryo morphology phenotype",
                        "aplasia or hypoplasia of radius bone",
                        "organ part atresia",
                        "body proper",
                        "gonad phenotype",
                        "germ layer / neural crest",
                        "intestine atresia",
                        "renal pelvis",
                        "male reproductive system",
                        "localised anatomical structure",
                        "decreased size of the bone of free limb or fin",
                        "autopod region phenotype",
                        "Abnormality of the genitourinary system",
                        "forelimb endochondral element",
                        "primary circulatory organ",
                        "anatomical entity atresia",
                        "Chromosome breakage",
                        "decreased length of skeletal element",
                        "multicellular organism",
                        "decreased size of the forelimb bone",
                        "Deviation of finger",
                        "main body axis",
                        "upper urinary tract phenotype",
                        "anatomical entity",
                        "embryonic structure",
                        "limb phenotype",
                        "process",
                        "multicellular anatomical structure",
                        "trunk",
                        "anlage phenotype",
                        "Upper limb undergrowth",
                        "Abnormal renal morphology",
                        "anterior region of body",
                        "abdominal segment of trunk",
                        "Abnormality of the upper urinary tract",
                        "anatomical system",
                        "forelimb zeugopod bone hypoplasia",
                        "decreased length of multicellular anatomical structure",
                        "upper urinary tract",
                        "limb long bone phenotype",
                        "genitourinary system",
                        "anatomical structure",
                        "cavitated compound organ phenotype",
                        "Renal cyst",
                        "external soft tissue zone phenotype",
                        "Abnormal skeletal morphology",
                        "absent material anatomical entity in the limb bud",
                        "thenar eminence hypoplasia",
                        "arm phenotype",
                        "kidney physiology phenotype",
                        "abdominal segment element",
                        "developing anatomical structure",
                        "phenotypic effect",
                        "Abnormal appendicular skeleton morphology",
                        "anatomical collection phenotype",
                        "skeletal system phenotype",
                        "anatomical cluster",
                        "forelimb morphology phenotype",
                        "mesenchyme morphology phenotype",
                        "forelimb bud phenotype",
                        "skeleton of limb phenotype",
                        "decreased size of the anatomical entity",
                        "lateral structure phenotype",
                        "deviation of anatomical entity",
                        "absent anatomical structure",
                        "trunk region element",
                        "decreased length of limb bone",
                        "thoracic segment organ phenotype",
                        "aplasia or hypoplasia of skeleton",
                        "anatomical conduit phenotype",
                        "Abnormality of limbs",
                        "forelimb zeugopod skeleton",
                        "biological_process phenotype",
                        "renal/urinary system phenotype",
                        "decreased length of anatomical entity",
                        "subdivision of organism along main body axis phenotype",
                        "mesenchyme phenotype",
                        "abdominal segment element phenotype",
                        "endochondral element phenotype",
                        "limb segment phenotype",
                        "abdomen element phenotype",
                        "agenesis of anatomical entity",
                        "Finger aplasia",
                        "Phenotypic abnormality",
                        "limb skeleton subdivision",
                        "independent continuant",
                        "anlage",
                        "size of anatomical entity phenotype",
                        "organ part",
                        "upper limb segment phenotype",
                        "compound organ phenotype",
                        "increased size of the anatomical structure",
                        "structure with developmental contribution from neural crest",
                        "material anatomical entity",
                        "reproductive structure phenotype",
                        "decreased length of digit 1",
                        "bone of pectoral complex morphology phenotype",
                        "decreased size of the anatomical structure in the pectoral complex",
                        "increased size of the organ part",
                        "organism subdivision",
                        "anatomical conduit",
                        "embryonic tissue",
                        "decreased length of manual digit",
                        "excretory system",
                        "endochondral element",
                        "Gastrointestinal atresia",
                        "Abnormality of the kidney",
                        "kidney mesenchyme morphology phenotype",
                        "lateral plate mesoderm phenotype",
                        "abdomen element",
                        "forelimb zeugopod phenotype",
                        "limb endochondral element phenotype",
                        "absent multicellular anatomical structure",
                        "Abnormality of the male genitalia",
                        "localised anatomical entity",
                        "absent anatomical structure in the multicellular organism",
                        "compound organ",
                        "kidney phenotype",
                        "Abnormality of the upper limb",
                        "lateral plate mesoderm morphology phenotype",
                        "increased size of the anatomical entity",
                        "organ system subdivision phenotype",
                        "embryo",
                        "external soft tissue zone",
                        "macromolecule metabolic process phenotype",
                        "organ",
                        "taxon specific phenotype",
                        "renal system",
                        "anatomical conduit atresia",
                        "viscus phenotype",
                        "cell",
                        "Abnormal cellular physiology",
                        "Dilatation of the renal pelvis",
                        "pectoral appendage",
                        "biosynthetic process phenotype",
                        "anatomical entity morphology phenotype",
                        "paired limb/fin segment phenotype",
                        "embryonic tissue phenotype",
                        "material entity",
                        "genitourinary system phenotype",
                        "presumptive structure",
                        "long bone morphology phenotype",
                        "limb long bone",
                        "ectoderm-derived structure phenotype",
                        "anatomical entity morphology in the skeleton of pectoral complex phenotype",
                        "anatomical cluster phenotype",
                        "subdivision of trunk phenotype",
                        "decreased length of bone of pectoral complex",
                        "renal pelvis morphology phenotype",
                        "forelimb zeugopod bone morphology phenotype",
                        "germ layer",
                        "continuant",
                        "mesoderm-derived structure phenotype",
                        "decreased length of endochondral element",
                        "decreased size of the arm bone",
                        "bone element",
                        "subdivision of organism along appendicular axis",
                        "forelimb zeugopod bone",
                        "structure with developmental contribution from neural crest phenotype",
                        "Abnormality of the urinary system",
                        "closing of the organ part",
                        "anus phenotype",
                        "entity",
                        "cavitated compound organ",
                        "manual digit phenotype",
                        "appendage musculature phenotype",
                        "metabolic process phenotype",
                        "phenotype",
                        "kidney mesenchyme phenotype",
                        "absent organism subdivision",
                        "kidney mesenchyme",
                        "organism subdivision phenotype",
                        "anatomical system atresia",
                        "heart morphology phenotype",
                        "homeostatic process",
                        "increased size of the multicellular anatomical structure",
                        "cell phenotype",
                        "limb",
                        "radius bone morphology phenotype",
                        "disconnected anatomical group",
                        "spatial pattern of anatomical entity phenotype",
                        "absent multicellular anatomical structure in the limb",
                        "germ layer phenotype",
                        "decreased size of the organism subdivision",
                        "embryonic structure phenotype",
                        "pathological entity",
                        "decreased size of the autopodial extension",
                        "dilated anatomical entity",
                        "Hydronephrosis",
                        "material anatomical entity phenotype",
                        "decreased size of the bone of appendage girdle complex",
                        "subdivision of skeletal system phenotype",
                        "appendage girdle complex",
                        "decreased size of the anatomical entity in the pectoral complex",
                        "regulation of macromolecule biosynthetic process",
                        "renal pelvis/ureter",
                        "embryo phenotype",
                        "decreased length of organism subdivision",
                        "subdivision of tube atresia",
                        "arm",
                        "subdivision of trunk",
                        "segment of manus",
                        "increased size of the renal pelvis",
                        "multicellular organism phenotype",
                        "limb bud",
                        "manual digit 1 or 5",
                        "subdivision of organism along appendicular axis phenotype",
                        "organ phenotype",
                        "digestive tract",
                        "mesenchyme",
                        "decreased length of arm bone",
                        "embryonic tissue morphology phenotype",
                        "forelimb skeleton",
                        "mesoderm-derived structure",
                        "reproductive structure",
                        "large intestine morphology phenotype",
                        "lateral structure",
                        "mesoderm morphology phenotype",
                        "decreased size of the multicellular anatomical structure",
                        "increased size of the material anatomical entity",
                        "regulation of biosynthetic process",
                        "paired limb/fin bud phenotype",
                        "palmar part of manus",
                        "manus morphology phenotype",
                        "Abnormality of the musculoskeletal system",
                        "localised reproductive organ",
                        "paired limb/fin phenotype",
                        "anatomical entity hypoplasia",
                        "anatomical entity morphology in the appendage girdle complex phenotype",
                        "absent autopodial extension",
                        "lateral plate mesoderm",
                        "paired limb/fin",
                        "zeugopod phenotype",
                        "Abnormal large intestine morphology",
                        "multicellular anatomical structure phenotype",
                        "skeletal element",
                        "forelimb bone",
                        "endochondral bone phenotype",
                        "Abnormal male external genitalia morphology",
                        "forelimb long bone",
                        "forelimb zeugopod",
                        "aplasia or hypoplasia of manual digit",
                        "radius endochondral element",
                        "Abnormal long bone morphology",
                        "Abnormality of the hand",
                        "localised male reproductive organ",
                        "limb long bone morphology phenotype",
                        "Aplasia/hypoplasia involving forearm bones",
                        "alimentary part of gastrointestinal system",
                        "subdivision of skeletal system",
                        "subdivision of tube phenotype",
                        "musculature",
                        "skeletal system",
                        "subdivision of skeleton",
                        "skeleton of pectoral complex",
                        "decreased size of the limb bone",
                        "appendicular skeleton",
                        "arm bone",
                        "gene expression",
                        "Abnormal morphology of the radius",
                        "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",
                        "Aplasia/hypoplasia involving bones of the hand",
                        "decreased size of the material anatomical entity",
                        "decreased length of bone of free limb or fin",
                        "anatomical entity length phenotype",
                        "paired limb/fin skeleton",
                        "Aplasia/Hypoplasia of fingers",
                        "pectoral appendage bud",
                        "cellular process phenotype",
                        "Abnormal forearm bone morphology",
                        "forelimb",
                        "macromolecule metabolic process",
                        "appendicular skeleton morphology phenotype",
                        "subdivision of organism along main body axis",
                        "germ layer morphology phenotype",
                        "appendage musculature",
                        "Abnormality of chromosome stability",
                        "Aplasia/hypoplasia involving bones of the extremities",
                        "decreased length of forelimb zeugopod bone",
                        "renal system morphology phenotype",
                        "forelimb long bone phenotype",
                        "manus phenotype",
                        "dense mesenchyme tissue phenotype",
                        "radius bone",
                        "cyst",
                        "large intestine phenotype",
                        "forelimb zeugopod bone phenotype",
                        "reproductive organ",
                        "pectoral appendage skeleton phenotype",
                        "Aplasia/hypoplasia of the extremities",
                        "multi-limb segment region",
                        "digestive system phenotype",
                        "multicellular organism morphology phenotype",
                        "localised multicellular anatomical structure",
                        "appendicular skeletal system",
                        "limb bud morphology phenotype",
                        "arm bone phenotype",
                        "renal system phenotype",
                        "manus",
                        "skeleton of limb",
                        "dense mesenchyme tissue",
                        "location of anatomical entity phenotype",
                        "reproductive system",
                        "digestive system morphology phenotype",
                        "orifice phenotype",
                        "Abnormal external genitalia morphology",
                        "Abnormal testis morphology",
                        "localised gonad",
                        "cellular organisms",
                        "testis",
                        "external male genitalia",
                        "increased size of the anatomical conduit",
                        "localised reproductive structure",
                        "gene expression phenotype",
                        "size of multicellular organism phenotype",
                        "Proximal placement of thumb",
                        "male organism phenotype",
                        "testis phenotype",
                        "male reproductive system phenotype",
                        "rectum atresia",
                        "male organism",
                        "decreased size of the long bone",
                        "external genitalia phenotype",
                        "pathological phenotype observation",
                        "multi-limb segment region phenotype",
                        "biological_process",
                        "muscle organ",
                        "localised testis",
                        "thoracic cavity element phenotype",
                        "localised organ",
                        "circulatory organ",
                        "Abnormality of the genital system",
                        "reproductive organ phenotype",
                        "gonad",
                        "pectoral appendage skeleton",
                        "aplastic anatomical entity",
                        "male reproductive organ",
                        "digit 1 or 5 phenotype",
                        "decreased size of the limb endochondral element",
                        "digit 1 plus metapodial segment",
                        "pectoral appendage phenotype",
                        "Abnormal finger morphology",
                        "Abnormality of body height",
                        "bone element phenotype",
                        "digit phenotype",
                        "Aplasia/Hypoplasia of the thumb",
                        "thoracic segment of trunk",
                        "macromolecule biosynthetic process phenotype",
                        "autopodial skeleton",
                        "digit plus metapodial segment",
                        "autopodial extension",
                        "forelimb zeugopod morphology phenotype",
                        "Abnormal thumb morphology",
                        "decreased length of manual digit 1",
                        "tissue phenotype",
                        "Short finger",
                        "thenar eminence",
                        "Short thumb",
                        "manual digit morphology in the manus phenotype",
                        "Abnormal digit morphology",
                        "embryonic autopod plate",
                        "Abnormal hand morphology",
                        "segment of autopod",
                        "absent material anatomical entity in the limb",
                        "number of anatomical enitites of type multicellular anatomical structure phenotype",
                        "Stage 5 chronic kidney disease",
                        "surface structure phenotype",
                        "decreased size of the digit",
                        "upper limb segment",
                        "manual digit 1 plus metapodial segment",
                        "decreased length of autopodial extension",
                        "absent material anatomical entity in the forelimb",
                        "Abnormal renal pelvis morphology",
                        "manual digit 1",
                        "tube",
                        "digitopodium region",
                        "acropodium region",
                        "manual digitopodium region",
                        "manual digit 1 morphology phenotype",
                        "embryonic autopod plate morphology phenotype",
                        "manual digit plus metapodial segment",
                        "organ part phenotype",
                        "absent anatomical structure in the limb",
                        "circulatory system phenotype",
                        "limb morphology phenotype",
                        "occurrent",
                        "digit",
                        "Deviation of the thumb",
                        "external male genitalia phenotype",
                        "Deviation of the hand or of fingers of the hand",
                        "deviation of manual digit",
                        "Short digit",
                        "number of anatomical enitites of type material anatomical entity phenotype",
                        "digit 1 or 5",
                        "absent material anatomical entity in the multicellular organism",
                        "Absent thumb",
                        "absent multicellular anatomical structure in the multicellular organism",
                        "absent anatomical entity in the multicellular organism",
                        "absent anatomical entity in the limb bud",
                        "absent anatomical entity",
                        "number of anatomical enitites of type anatomical structure phenotype",
                        "absent multicellular anatomical structure in the forelimb",
                        "decreased size of the anatomical structure",
                        "manual digit",
                        "skeleton of manus",
                        "absent anatomical entity in the limb",
                        "decreased size of the bone element",
                        "Abnormal cellular phenotype",
                        "absent anatomical entity in the forelimb",
                        "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",
                        "negative regulation of macromolecule metabolic process",
                        "Metazoa",
                        "absent manual digit",
                        "abdominal segment element physiology phenotype",
                        "absent organism subdivision in the multicellular organism",
                        "Limb undergrowth",
                        "musculature of body",
                        "number of anatomical enitites of type organism subdivision phenotype",
                        "aplastic manual digit 1",
                        "subdivision of digestive tract atresia",
                        "heart phenotype",
                        "Abnormal heart morphology",
                        "anatomical entity phenotype",
                        "thoracic cavity element",
                        "cardiovascular system morphology phenotype",
                        "trunk phenotype",
                        "Abnormal cardiovascular system morphology",
                        "primary circulatory organ phenotype",
                        "cardiovascular system",
                        "circulatory organ phenotype",
                        "autopod region",
                        "circulatory system",
                        "localised material anatomical entity",
                        "viscus",
                        "Abnormality of the cardiovascular system",
                        "decreased length of organ",
                        "developmental or adult structural  defect",
                        "pathological anatomical entity",
                        "negative regulation of metabolic process",
                        "Abnormality of the musculature of the limbs",
                        "regulation of macromolecule metabolic process",
                        "Abnormality of metabolism/homeostasis",
                        "metabolic process",
                        "decreased length of digit",
                        "negative regulation of biological process",
                        "regulation of cellular process",
                        "programmed DNA elimination",
                        "biological regulation phenotype",
                        "mesoderm",
                        "macromolecule biosynthetic process",
                        "decreased height of the anatomical entity",
                        "aplasia or hypoplasia of manual digit 1",
                        "regulation of metabolic process",
                        "negative regulation of macromolecule biosynthetic process",
                        "regulation of gene expression",
                        "homeostatic process phenotype",
                    ],
                    "highlighting": None,
                },
                {
                    "id": "MONDO:0013499",
                    "category": "biolink:Disease",
                    "name": "Fanconi anemia complementation group P",
                    "description": "Any Fanconi anemia in which the cause of the disease is a mutation in the SLX4 gene.",
                    "provided_by": "phenio_nodes",
                    "xref": ["DOID:0111092", "GARD:15731", "MEDGEN:854020", "OMIM:613951", "UMLS:C3469542"],
                    "synonym": [
                        "FANCP",
                        "Fanconi Anemia, complementation group type P",
                        "Fanconi anaemia caused by mutation in SLX4",
                        "Fanconi anaemia caused by mutation in Slx4",
                        "Fanconi anaemia complementation group type P",
                        "Fanconi anemia caused by mutation in SLX4",
                        "Fanconi anemia caused by mutation in Slx4",
                        "Fanconi anemia complementation group type P",
                        "Fanconi anemia, complementation group P",
                        "SLX4 Fanconi anaemia",
                        "SLX4 Fanconi anemia",
                        "Slx4 Fanconi anaemia",
                        "Slx4 Fanconi anemia",
                    ],
                    "exact_synonyms": [
                        "FANCP|Fanconi Anemia, complementation group type P|Fanconi anaemia caused by mutation in SLX4|Fanconi anaemia caused by mutation in Slx4|Fanconi anaemia complementation group type P|Fanconi anemia caused by mutation in SLX4|Fanconi anemia caused by mutation in Slx4|Fanconi anemia complementation group type P|SLX4 Fanconi anaemia|SLX4 Fanconi anemia|Slx4 Fanconi anaemia|Slx4 Fanconi anemia"
                    ],
                    "related_synonyms": ["Fanconi anemia, complementation group P"],
                    "subsets": ["gard_rare", "nord_rare", "otar", "rare"],
                    "namespace": "MONDO",
                    "has_phenotype": [
                        "HP:0001876",
                        "HP:0000347",
                        "HP:0009778",
                        "HP:0001510",
                        "HP:0000414",
                        "HP:0000957",
                        "HP:0001903",
                        "HP:0012745",
                        "HP:0000085",
                        "HP:0003221",
                        "HP:0004322",
                        "HP:0000365",
                        "HP:0000252",
                        "HP:0002984",
                        "HP:0000028",
                        "HP:0000125",
                        "HP:0009777",
                        "HP:0000581",
                        "HP:0002860",
                        "HP:0001045",
                    ],
                    "has_phenotype_label": [
                        "Pancytopenia",
                        "Micrognathia",
                        "Short thumb",
                        "Growth delay",
                        "Bulbous nose",
                        "Cafe-au-lait spot",
                        "Anemia",
                        "Short palpebral fissure",
                        "Horseshoe kidney",
                        "Chromosomal breakage induced by crosslinking agents",
                        "Short stature",
                        "Hearing impairment",
                        "Microcephaly",
                        "Hypoplasia of the radius",
                        "Cryptorchidism",
                        "Pelvic kidney",
                        "Absent thumb",
                        "Blepharophimosis",
                        "Squamous cell carcinoma",
                        "Vitiligo",
                    ],
                    "has_phenotype_count": 20,
                    "has_phenotype_closure": [
                        "HP:0002664",
                        "HP:0011793",
                        "HP:0002860",
                        "HP:0000581",
                        "UPHENO:0026078",
                        "UPHENO:0026506",
                        "UPHENO:0009146",
                        "UPHENO:0011572",
                        "HP:0009777",
                        "UPHENO:0081451",
                        "UPHENO:0026640",
                        "UPHENO:0011825",
                        "UPHENO:0026757",
                        "UPHENO:0011536",
                        "UPHENO:0009020",
                        "UPHENO:0009163",
                        "UPHENO:0027017",
                        "UPHENO:0009382",
                        "UPHENO:0026108",
                        "UPHENO:0026146",
                        "UPHENO:0026181",
                        "UPHENO:0053633",
                        "UPHENO:0053643",
                        "UPHENO:0053588",
                        "HP:0000086",
                        "HP:0000078",
                        "UPHENO:0053571",
                        "UPHENO:0053572",
                        "UPHENO:0053644",
                        "UBERON:0000079",
                        "HP:0012243",
                        "UPHENO:0053580",
                        "UPHENO:0002682",
                        "UPHENO:0053561",
                        "UBERON:0000990",
                        "UPHENO:0053566",
                        "UPHENO:0003055",
                        "UPHENO:0002523",
                        "HP:0000028",
                        "UPHENO:0053559",
                        "UPHENO:0053647",
                        "HP:0000035",
                        "UBERON:0004176",
                        "UBERON:0003135",
                        "UBERON:0000991",
                        "UPHENO:0069328",
                        "UPHENO:0068838",
                        "UPHENO:0069030",
                        "UPHENO:0046460",
                        "UPHENO:0046465",
                        "UPHENO:0004173",
                        "UBERON:0010703",
                        "UBERON:0002471",
                        "UBERON:0003606",
                        "UBERON:0010741",
                        "UBERON:0003460",
                        "UBERON:0001423",
                        "HP:0040070",
                        "HP:0009821",
                        "HP:0002984",
                        "UBERON:0002386",
                        "UPHENO:0046392",
                        "UPHENO:0046479",
                        "UPHENO:0069194",
                        "UPHENO:0002785",
                        "UPHENO:0068932",
                        "UPHENO:0086956",
                        "HP:0003026",
                        "UPHENO:0087501",
                        "UBERON:0011584",
                        "UBERON:0002495",
                        "UPHENO:0068921",
                        "UPHENO:0076754",
                        "UPHENO:0069046",
                        "UPHENO:0025509",
                        "UPHENO:0046594",
                        "UPHENO:0069047",
                        "UPHENO:0004595",
                        "UPHENO:0046472",
                        "UPHENO:0075944",
                        "UPHENO:0076718",
                        "UPHENO:0069064",
                        "UPHENO:0068912",
                        "HP:0009826",
                        "UPHENO:0046455",
                        "UPHENO:0002637",
                        "UPHENO:0002967",
                        "UPHENO:0046540",
                        "UPHENO:0046397",
                        "UBERON:0000955",
                        "HP:0000240",
                        "UPHENO:0087518",
                        "UPHENO:0076791",
                        "UPHENO:0076805",
                        "HP:0002060",
                        "UPHENO:0002594",
                        "UBERON:0000073",
                        "UPHENO:0087363",
                        "HP:0000252",
                        "HP:0002977",
                        "UBERON:0001016",
                        "UPHENO:0005285",
                        "UBERON:0003914",
                        "HP:0012639",
                        "HP:0040195",
                        "HP:0000707",
                        "UPHENO:0004484",
                        "UBERON:0001049",
                        "UBERON:0003080",
                        "UPHENO:0026010",
                        "UPHENO:0081313",
                        "UPHENO:0004521",
                        "UBERON:0002616",
                        "UPHENO:0004523",
                        "UPHENO:0003001",
                        "UPHENO:0003004",
                        "UPHENO:0002736",
                        "UPHENO:0076799",
                        "GO:0032501",
                        "GO:0050954",
                        "UPHENO:0002211",
                        "UPHENO:0005513",
                        "UPHENO:0002385",
                        "UPHENO:0002308",
                        "UPHENO:0002386",
                        "GO:0003008",
                        "UBERON:0002105",
                        "UPHENO:0005433",
                        "UPHENO:0002685",
                        "GO:0007605",
                        "UPHENO:0050234",
                        "UPHENO:0005512",
                        "UPHENO:0005437",
                        "UPHENO:0002240",
                        "UPHENO:0052161",
                        "UPHENO:0050625",
                        "UPHENO:0081423",
                        "UPHENO:0069254",
                        "UPHENO:0003056",
                        "UPHENO:0081424",
                        "HP:0000002",
                        "UPHENO:0050065",
                        "HP:0003220",
                        "HP:0025354",
                        "GO:0060255",
                        "HP:0002818",
                        "GO:0009889",
                        "UBERON:0015001",
                        "GO:0010558",
                        "GO:0048519",
                        "GO:0043170",
                        "UPHENO:0049873",
                        "GO:0008152",
                        "UPHENO:0052159",
                        "HP:0001939",
                        "UPHENO:0050007",
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                        "UPHENO:0003163",
                        "UPHENO:0002837",
                        "UPHENO:0005016",
                        "UPHENO:0012274",
                        "UPHENO:0087430",
                        "UPHENO:0087950",
                        "UPHENO:0001025",
                        "UPHENO:0002896",
                        "UBERON:0003050",
                        "UBERON:0001048",
                        "UPHENO:0002715",
                        "UPHENO:0005596",
                        "UPHENO:0002651",
                        "UBERON:0001032",
                        "GO:0010629",
                        "UPHENO:0005008",
                        "HP:0001877",
                        "UBERON:0005497",
                        "UPHENO:0076800",
                        "UBERON:0000004",
                        "UPHENO:0084715",
                        "UBERON:0000076",
                        "HP:0000953",
                        "UPHENO:0052231",
                        "HP:0001574",
                        "HP:0012733",
                        "UBERON:0034923",
                        "UPHENO:0054957",
                        "UPHENO:0080662",
                        "UPHENO:0068848",
                        "UBERON:0002097",
                        "UPHENO:0003811",
                        "UBERON:0001893",
                        "UPHENO:0080377",
                        "UPHENO:0046484",
                        "HP:0000951",
                        "UPHENO:0001303",
                        "UPHENO:0004434",
                        "UPHENO:0086172",
                    ],
                    "has_phenotype_closure_label": [
                        "Vitiligo",
                        "Neoplasm",
                        "aplastic manual digit 1",
                        "absent anatomical structure in the multicellular organism",
                        "absent multicellular anatomical structure in the limb",
                        "absent organism subdivision in the multicellular organism",
                        "number of anatomical enitites of type anatomical entity phenotype",
                        "absent digit",
                        "absent material anatomical entity in the forelimb",
                        "Finger aplasia",
                        "absent anatomical entity",
                        "absent anatomical structure",
                        "absent anatomical entity in the limb bud",
                        "absent multicellular anatomical structure in the multicellular organism",
                        "absent anatomical entity in the multicellular organism",
                        "number of anatomical enitites of type multicellular anatomical structure phenotype",
                        "absent material anatomical entity in the limb",
                        "Absent thumb",
                        "absent material anatomical entity in the limb bud",
                        "Pelvic kidney",
                        "localised trunk region element",
                        "localised cavitated compound organ",
                        "Ectopic kidney",
                        "external genitalia",
                        "male reproductive organ",
                        "reproductive structure phenotype",
                        "reproductive organ phenotype",
                        "Abnormality of the genital system",
                        "localised organ",
                        "absent multicellular anatomical structure",
                        "Abnormality of the male genitalia",
                        "localised anatomical structure",
                        "male reproductive system",
                        "male reproductive system phenotype",
                        "gonad phenotype",
                        "Cryptorchidism",
                        "localised reproductive structure",
                        "external male genitalia",
                        "reproductive structure",
                        "localised gonad",
                        "Abnormal testis morphology",
                        "localised anatomical entity",
                        "reproductive system phenotype",
                        "localised male reproductive organ",
                        "location of anatomical entity phenotype",
                        "arm bone phenotype",
                        "decreased size of the forelimb bone",
                        "forelimb zeugopod bone phenotype",
                        "decreased length of forelimb zeugopod bone",
                        "decreased length of bone of pectoral complex",
                        "decreased size of the mesoderm-derived structure",
                        "decreased size of the endochondral bone",
                        "radius bone",
                        "long bone phenotype",
                        "limb long bone morphology phenotype",
                        "Aplasia/hypoplasia involving forearm bones",
                        "Abnormal long bone morphology",
                        "radius endochondral element",
                        "forelimb zeugopod",
                        "forelimb bone",
                        "forelimb endochondral element phenotype",
                        "decreased length of bone element",
                        "decreased length of forelimb bone",
                        "decreased size of the endochondral element",
                        "forelimb zeugopod skeleton",
                        "forelimb endochondral element",
                        "bone of pectoral complex",
                        "decreased length of organ",
                        "decreased size of the bone of pectoral complex",
                        "zeugopod phenotype",
                        "decreased length of limb bone",
                        "forelimb bone phenotype",
                        "decreased size of the organ",
                        "decreased length of arm bone",
                        "zeugopodial skeleton",
                        "long bone",
                        "Upper limb undergrowth",
                        "decreased length of endochondral bone",
                        "Aplasia/Hypoplasia of the radius",
                        "external genitalia phenotype",
                        "decreased size of the long bone",
                        "decreased length of skeletal element",
                        "decreased size of the forelimb zeugopod bone",
                        "forelimb skeleton phenotype",
                        "decreased size of the skeletal element",
                        "Abnormal upper limb bone morphology",
                        "bone of pectoral complex phenotype",
                        "limb long bone",
                        "long bone morphology phenotype",
                        "Short long bone",
                        "aplasia or hypoplasia of radius bone",
                        "forelimb zeugopod bone hypoplasia",
                        "Abnormality of skull size",
                        "Abnormality of the nervous system",
                        "Aplasia/Hypoplasia involving the central nervous system",
                        "central nervous system",
                        "telencephalon morphology phenotype",
                        "Microcephaly",
                        "Abnormal forebrain morphology",
                        "regional part of nervous system",
                        "regional part of brain",
                        "localised lateral structure",
                        "Abnormal brain morphology",
                        "forebrain morphology phenotype",
                        "decreased size of the forelimb endochondral element",
                        "central nervous system morphology phenotype",
                        "absent anatomical entity in the forelimb",
                        "forebrain",
                        "brain",
                        "Abnormal cerebral morphology",
                        "nervous system morphology phenotype",
                        "epithelial tube",
                        "epithelial tube phenotype",
                        "Squamous cell carcinoma",
                        "neural tube phenotype",
                        "forebrain phenotype",
                        "Abnormal nervous system morphology",
                        "anterior neural tube",
                        "anterior neural tube phenotype",
                        "decreased sensory perception of mechanical stimulus",
                        "Abnormal ear physiology",
                        "material anatomical entity physiology phenotype",
                        "decreased nervous system process",
                        "structure with developmental contribution from neural crest physiology phenotype",
                        "multicellular organismal process",
                        "multicellular anatomical structure physiology phenotype",
                        "decreased biological_process",
                        "Hearing impairment",
                        "nervous system process phenotype",
                        "anatomical structure physiology phenotype",
                        "decreased multicellular organismal process",
                        "organ physiology phenotype",
                        "ear physiology phenotype",
                        "decreased qualitatively system process",
                        "absent multicellular anatomical structure in the forelimb",
                        "sensory perception of sound phenotype",
                        "sensory perception of sound",
                        "number of anatomical enitites of type anatomical structure phenotype",
                        "system process",
                        "decreased qualitatively sensory perception of sound",
                        "sensory perception of mechanical stimulus",
                        "gonad",
                        "sense organ physiology phenotype",
                        "decreased sensory perception",
                        "male organism phenotype",
                        "size of multicellular organism phenotype",
                        "decreased size of the multicellular organism",
                        "anatomical entity height phenotype",
                        "Short stature",
                        "decreased height of the multicellular organism",
                        "programmed DNA elimination by chromosome breakage",
                        "biological regulation phenotype",
                        "Chromosomal breakage induced by crosslinking agents",
                        "regional part of brain phenotype",
                        "regulation of gene expression",
                        "negative regulation of macromolecule biosynthetic process",
                        "cellular process",
                        "cellular process phenotype",
                        "decreased size of the bone element",
                        "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",
                        "Chromosome breakage",
                        "homeostatic process",
                        "biological regulation",
                        "biosynthetic process phenotype",
                        "Abnormality of chromosome stability",
                        "negative regulation of biosynthetic process",
                        "negative regulation of macromolecule metabolic process",
                        "regulation of macromolecule metabolic process",
                        "regulation of biosynthetic process",
                        "negative regulation of metabolic process",
                        "Abnormal morphology of the radius",
                        "gene expression",
                        "abdominal segment of trunk",
                        "trunk",
                        "Abnormality of the kidney",
                        "Abnormality of the genitourinary system",
                        "trunk phenotype",
                        "negative regulation of gene expression phenotype",
                        "trunk region element phenotype",
                        "subdivision of trunk phenotype",
                        "compound organ",
                        "vestibulo-auditory system phenotype",
                        "renal system",
                        "kidney phenotype",
                        "kidney morphology phenotype",
                        "shape of anatomical entity phenotype",
                        "concave 3-D shape anatomical entity",
                        "shape of kidney phenotype",
                        "Abnormal localization of kidney",
                        "U-shaped anatomical entity",
                        "abdomen element",
                        "shape of continuant phenotype",
                        "limb long bone phenotype",
                        "genitourinary system",
                        "excretory system",
                        "abdomen",
                        "trunk region element",
                        "kidney",
                        "upper urinary tract",
                        "abdominal segment element phenotype",
                        "pre-chordal neural plate",
                        "immature eye",
                        "palpebral fissure phenotype",
                        "homeostatic process phenotype",
                        "Short palpebral fissure",
                        "ocular adnexa",
                        "optic cup",
                        "visual system phenotype",
                        "bone of pectoral complex morphology phenotype",
                        "neural tube morphology phenotype",
                        "eyelid",
                        "localised testis",
                        "optic vesicle phenotype",
                        "eyelid phenotype",
                        "eye primordium phenotype",
                        "immature eye phenotype",
                        "Forearm undergrowth",
                        "optic vesicle",
                        "camera-type eye phenotype",
                        "Horseshoe kidney",
                        "decreased length of anatomical conduit",
                        "camera-type eye morphology phenotype",
                        "brain morphology phenotype",
                        "visual system",
                        "decreased length of ectoderm-derived structure",
                        "Abnormality of the palpebral fissures",
                        "eye phenotype",
                        "epithelium",
                        "obsolete cell",
                        "digestive system",
                        "multi-tissue structure phenotype",
                        "forelimb long bone",
                        "facial skeleton phenotype",
                        "material anatomical entity",
                        "autopod region",
                        "decreased length of digit 1",
                        "Hypoplasia of the radius",
                        "negative regulation of gene expression",
                        "future central nervous system phenotype",
                        "telencephalon phenotype",
                        "dermal skeletal element phenotype",
                        "metabolic process phenotype",
                        "phenotype",
                        "ectoderm",
                        "embryonic structure phenotype",
                        "germ layer phenotype",
                        "decreased size of the organism subdivision",
                        "head bone morphology phenotype",
                        "camera-type eye",
                        "skeleton of lower jaw",
                        "organism subdivision phenotype",
                        "postcranial axial skeletal system",
                        "primary subdivision of skull",
                        "digestive system element phenotype",
                        "skull",
                        "jaw skeleton",
                        "paired limb/fin bud phenotype",
                        "Aplasia/Hypoplasia of the cerebrum",
                        "jaw region",
                        "Phenotypic abnormality",
                        "hematopoietic system",
                        "limb skeleton subdivision",
                        "compound organ phenotype",
                        "craniocervical region phenotype",
                        "oxygen accumulating cell",
                        "pectoral appendage",
                        "aplasia or hypoplasia of anatomical entity",
                        "musculoskeletal system phenotype",
                        "localised abdominal segment element",
                        "primary subdivision of cranial skeletal system",
                        "increased volume of anatomical entity",
                        "facial bone",
                        "ear",
                        "Abnormality of the ear",
                        "bone of appendage girdle complex phenotype",
                        "membrane bone",
                        "palpebral fissure",
                        "motile cell",
                        "facial skeleton morphology phenotype",
                        "dermatocranium",
                        "craniocervical region morphology phenotype",
                        "integumental system phenotype",
                        "subdivision of skeletal system",
                        "head",
                        "Abnormal renal morphology",
                        "neurogenic placode phenotype",
                        "decreased length of orifice",
                        "intramembranous bone phenotype",
                        "Hyperpigmentation of the skin",
                        "subdivision of skeleton phenotype",
                        "decreased qualitatively sensory perception",
                        "neural plate",
                        "U-shaped kidney",
                        "Abnormal ocular adnexa morphology",
                        "limb endochondral element",
                        "paired limb/fin bud",
                        "central nervous system phenotype",
                        "pectoral appendage bud",
                        "Abnormality of the orbital region",
                        "sensory system phenotype",
                        "subdivision of tube",
                        "bone marrow",
                        "Abnormality of metabolism/homeostasis",
                        "zone of organ",
                        "neural fold phenotype",
                        "skeleton phenotype",
                        "musculature of body phenotype",
                        "anatomical point",
                        "Pancytopenia",
                        "neural plate morphology phenotype",
                        "mandible morphology phenotype",
                        "paired limb/fin segment",
                        "digit 1 phenotype",
                        "protuberance",
                        "localised multicellular anatomical structure",
                        "digestive system phenotype",
                        "multicellular organism morphology phenotype",
                        "pharyngeal arch 1",
                        "bone of lower jaw",
                        "facial skeleton",
                        "aplasia or hypoplasia of skull",
                        "Abnormality of blood and blood-forming tissues",
                        "Aplasia/Hypoplasia of the thumb",
                        "mandible",
                        "membrane bone phenotype",
                        "Abnormal size of the palpebral fissures",
                        "skull phenotype",
                        "embryonic autopod plate morphology phenotype",
                        "dentary phenotype",
                        "limb bone morphology phenotype",
                        "germ layer / neural crest phenotype",
                        "dermal skeleton",
                        "regional part of nervous system phenotype",
                        "face phenotype",
                        "anatomical entity hypoplasia in face",
                        "jaw skeleton morphology phenotype",
                        "Opisthokonta",
                        "foregut phenotype",
                        "embryo morphology phenotype",
                        "bone of lower jaw phenotype",
                        "pharyngeal arch",
                        "mandibular prominence morphology phenotype",
                        "body proper",
                        "localised kidney",
                        "craniocervical region",
                        "bone cell",
                        "manual digit 1",
                        "main body axis",
                        "bone of craniocervical region phenotype",
                        "axial skeletal system",
                        "multicellular organism",
                        "Blepharophimosis",
                        "Abnormal bone marrow cell morphology",
                        "anatomical entity length phenotype",
                        "Neoplasm by anatomical site",
                        "ecto-epithelium",
                        "neural groove phenotype",
                        "Aplasia/hypoplasia involving the skeleton",
                        "skeletal element phenotype",
                        "presumptive structure phenotype",
                        "skeleton",
                        "decreased size of the ectoderm-derived structure",
                        "anatomical collection",
                        "nucleate cell",
                        "dentary",
                        "decreased length of digit 1 or 5",
                        "neural crest",
                        "musculature phenotype",
                        "immune system",
                        "forelimb bud morphology phenotype",
                        "increased size of the nose",
                        "zeugopod",
                        "decreased length of palpebral fissure",
                        "foregut",
                        "hematopoietic system phenotype",
                        "regulation of biological process",
                        "optic cup morphology phenotype",
                        "Abnormality of the skeletal system",
                        "material entity",
                        "dermal skeleton phenotype",
                        "presumptive ectoderm phenotype",
                        "multi organ part structure phenotype",
                        "neoplasm phenotype",
                        "decreased system process",
                        "biogenic amine secreting cell",
                        "cranial placode",
                        "olfactory placode morphology phenotype",
                        "programmed DNA elimination",
                        "orbital region",
                        "hematopoietic cell",
                        "skull morphology phenotype",
                        "bone of jaw phenotype",
                        "bone of free limb or fin phenotype",
                        "paired limb/fin skeleton phenotype",
                        "head morphology phenotype",
                        "ectoderm-derived structure",
                        "renal/urinary system phenotype",
                        "biological_process phenotype",
                        "sensory system",
                        "subdivision of digestive tract",
                        "developing anatomical structure phenotype",
                        "decreased qualitatively multicellular organismal process",
                        "Abnormality of the ocular adnexa",
                        "neural plate phenotype",
                        "immaterial anatomical entity",
                        "anatomical collection phenotype",
                        "decreased size of the autopodial extension",
                        "reproductive system",
                        "Aplasia/Hypoplasia of the mandible",
                        "size of skull phenotype",
                        "growth phenotype",
                        "embryonic tissue phenotype",
                        "mandibular prominence",
                        "hemolymphoid system",
                        "bone element hypoplasia in face",
                        "musculature",
                        "subdivision of tube phenotype",
                        "surface structure",
                        "radius bone morphology phenotype",
                        "erythroid lineage cell",
                        "germ layer",
                        "absent material anatomical entity",
                        "decreased length of mesoderm-derived structure",
                        "decreased length of bone of appendage girdle complex",
                        "tissue",
                        "bone of craniocervical region",
                        "increased size of the ectoderm-derived structure",
                        "Aplasia/hypoplasia affecting bones of the axial skeleton",
                        "forelimb bud",
                        "taxon specific phenotype",
                        "Abnormality of the upper urinary tract",
                        "secretory cell",
                        "lateral structure phenotype",
                        "Eukaryota",
                        "eukaryotic cell",
                        "upper limb segment phenotype",
                        "anatomical conduit phenotype",
                        "Abnormality of limbs",
                        "Abnormal external genitalia morphology",
                        "digestive system morphology phenotype",
                        "orifice phenotype",
                        "embryonic tissue morphology phenotype",
                        "anatomical entity morphology phenotype",
                        "Hypermelanotic macule",
                        "pigmentation phenotype",
                        "organ part",
                        "size of anatomical entity phenotype",
                        "multicellular anatomical structure phenotype",
                        "nervous system",
                        "subdivision of digestive tract phenotype",
                        "dermal skeletal element",
                        "neural crest phenotype",
                        "skeletal element",
                        "mesoderm phenotype",
                        "cavitated compound organ phenotype",
                        "pharyngeal arch morphology phenotype",
                        "anatomical structure",
                        "negative regulation of cellular process",
                        "Abnormality of the head",
                        "epithelial fold phenotype",
                        "3-D shape anatomical entity",
                        "continuant",
                        "decreased size of the arm bone",
                        "decreased length of endochondral element",
                        "mesoderm-derived structure phenotype",
                        "pharyngeal arch system",
                        "anatomical entity hypoplasia",
                        "disconnected anatomical group",
                        "Abnormality of multiple cell lineages in the bone marrow",
                        "aplastic anatomical entity",
                        "pectoral appendage skeleton",
                        "phenotypic effect",
                        "developing anatomical structure",
                        "facial bone phenotype",
                        "myeloid cell",
                        "nervous system phenotype",
                        "platelet",
                        "independent continuant",
                        "increased size of the sense organ",
                        "epithelium phenotype",
                        "cavitated compound organ",
                        "manual digit phenotype",
                        "growth",
                        "ectodermal placode phenotype",
                        "limb bud",
                        "Growth abnormality",
                        "anatomical system",
                        "absent anatomical structure in the limb",
                        "organ part phenotype",
                        "decreased length of long bone",
                        "pharyngeal region of foregut",
                        "pharyngeal arch 1 morphology phenotype",
                        "Abnormal limb bone morphology",
                        "neurectoderm",
                        "forelimb zeugopod bone",
                        "subdivision of organism along appendicular axis",
                        "bone element",
                        "anucleate cell",
                        "radius bone phenotype",
                        "increased pigmentation in skin of body",
                        "dermal bone phenotype",
                        "subdivision of organism along main body axis phenotype",
                        "facial bone hypoplasia",
                        "protuberance phenotype",
                        "aplasia or hypoplasia of telencephalon",
                        "manual digit plus metapodial segment",
                        "musculoskeletal system",
                        "regulation of macromolecule biosynthetic process",
                        "decreased size of the anatomical entity in the pectoral complex",
                        "manus morphology phenotype",
                        "Abnormality of the musculoskeletal system",
                        "localised reproductive organ",
                        "paired limb/fin phenotype",
                        "arm bone",
                        "neural groove",
                        "Abnormal eyelid morphology",
                        "integument phenotype",
                        "increased size of the organ",
                        "structure with developmental contribution from neural crest phenotype",
                        "neural crest-derived structure",
                        "upper urinary tract phenotype",
                        "nose tip phenotype",
                        "postcranial axial skeleton",
                        "anatomical conduit",
                        "process",
                        "multicellular anatomical structure",
                        "multicellular organism height phenotype",
                        "All",
                        "subdivision of head",
                        "anatomical structure phenotype",
                        "decreased length of forelimb endochondral element",
                        "neurogenic placode",
                        "face",
                        "decreased length of manual digit 1",
                        "absent manual digit",
                        "Metazoa",
                        "non-connected functional system",
                        "anatomical point phenotype",
                        "testis phenotype",
                        "pigmentation",
                        "simple eye",
                        "germ layer / neural crest",
                        "olfactory organ phenotype",
                        "mouth",
                        "embryonic craniocervical region",
                        "cell",
                        "axial skeleton plus cranial skeleton",
                        "aplasia or hypoplasia of mandible",
                        "sensory perception phenotype",
                        "anatomical entity morphology in the pectoral complex phenotype",
                        "skeletal system morphology phenotype",
                        "anatomical entity",
                        "embryonic structure",
                        "radius bone hypoplasia",
                        "mandible hypoplasia",
                        "simple eye phenotype",
                        "multicellular organism phenotype",
                        "zone of organ phenotype",
                        "digit plus metapodial segment",
                        "agenesis of anatomical entity",
                        "size of palpebral fissure phenotype",
                        "craniofacial/craniocervical phenotype",
                        "structure with developmental contribution from neural crest",
                        "increased size of the anatomical structure",
                        "neural crest morphology phenotype",
                        "primary subdivision of skull phenotype",
                        "aplasia or hypoplasia of skeleton",
                        "multi organ part structure",
                        "testis",
                        "cellular organisms",
                        "Abnormal forearm bone morphology",
                        "forelimb",
                        "multi-tissue structure",
                        "organism subdivision",
                        "abdominal segment element",
                        "serotonin secreting cell",
                        "embryo phenotype",
                        "decreased length of organism subdivision",
                        "Neoplasm of the skin",
                        "subdivision of trunk",
                        "ectoderm phenotype",
                        "material anatomical entity phenotype",
                        "tube phenotype",
                        "erythrocyte",
                        "pectoral appendage bud phenotype",
                        "Abnormal jaw morphology",
                        "mesoderm-derived structure",
                        "forelimb skeleton",
                        "germ layer morphology phenotype",
                        "subdivision of organism along main body axis",
                        "decreased size of the anatomical structure in the pectoral complex",
                        "Abnormality of the skin",
                        "head phenotype",
                        "subdivision of skeleton",
                        "Abnormal axial skeleton morphology",
                        "Abnormal facial skeleton morphology",
                        "intramembranous bone",
                        "sensory perception",
                        "future nervous system",
                        "skeletal system",
                        "dermal bone",
                        "mouth phenotype",
                        "Hearing abnormality",
                        "embryonic tissue",
                        "decreased length of manual digit",
                        "presumptive ectoderm",
                        "dense mesenchyme tissue phenotype",
                        "genitourinary system phenotype",
                        "presumptive structure",
                        "male organism",
                        "Morphological central nervous system abnormality",
                        "increased size of the organism subdivision",
                        "anatomical entity phenotype",
                        "system process phenotype",
                        "bone of appendage girdle complex",
                        "Micrognathia",
                        "Abnormal erythrocyte morphology",
                        "pharyngeal arch 1 phenotype",
                        "orifice",
                        "male reproductive organ phenotype",
                        "neurectoderm phenotype",
                        "pharyngeal arch phenotype",
                        "appendage",
                        "anatomical system phenotype",
                        "lower jaw region",
                        "subdivision of head phenotype",
                        "anterior region of body",
                        "Macule",
                        "organ system subdivision",
                        "foregut morphology phenotype",
                        "number of anatomical enitites of type material anatomical entity phenotype",
                        "Short digit",
                        "decreased sensory perception of sound",
                        "bone of jaw",
                        "absent material anatomical entity in the multicellular organism",
                        "digit 1 or 5",
                        "oral opening",
                        "mesenchyme",
                        "digestive tract",
                        "digit 1",
                        "delayed growth",
                        "pre-chordal neural plate phenotype",
                        "skeletal system phenotype",
                        "blastula",
                        "multicellular organismal process phenotype",
                        "gastrula",
                        "skeleton of lower jaw phenotype",
                        "Abnormal skull morphology",
                        "absent anatomical structure in the forelimb",
                        "Abnormality of the nose",
                        "macromolecule metabolic process phenotype",
                        "organ",
                        "external soft tissue zone",
                        "gastrula morphology phenotype",
                        "decreased size of the multicellular anatomical structure in the pectoral complex",
                        "number of anatomical enitites of type organism subdivision phenotype",
                        "Limb undergrowth",
                        "musculature of body",
                        "Cafe-au-lait spot",
                        "root",
                        "bone marrow cell",
                        "lateral structure",
                        "absent organism subdivision",
                        "erythroid lineage cell morphology phenotype",
                        "Eumetazoa",
                        "unilaminar epithelium",
                        "digit 1 or 5 phenotype",
                        "Aplasia/Hypoplasia of fingers",
                        "paired limb/fin skeleton",
                        "paired limb/fin segment phenotype",
                        "absent autopodial extension",
                        "lateral plate mesoderm",
                        "decreased size of the bone of appendage girdle complex",
                        "subdivision of skeletal system phenotype",
                        "appendage girdle complex",
                        "decreased qualitatively nervous system process",
                        "paired limb/fin",
                        "decreased size of the palpebral fissure",
                        "external nose",
                        "decreased size of the limb endochondral element",
                        "digit 1 plus metapodial segment",
                        "decreased qualitatively biological_process",
                        "endochondral element",
                        "multi-limb segment region",
                        "decreased length of anatomical entity",
                        "orbital region phenotype",
                        "eyelid morphology phenotype",
                        "Abnormality of the upper limb",
                        "eye",
                        "head bone phenotype",
                        "decreased length of material anatomical entity",
                        "decreased length of manual digit 1 or 5",
                        "autopodial extension phenotype",
                        "pectoral appendage phenotype",
                        "Abnormal finger morphology",
                        "leukocyte",
                        "appendicular skeleton phenotype",
                        "sense organ phenotype",
                        "limb skeleton subdivision phenotype",
                        "decreased size of the material anatomical entity in the pectoral complex",
                        "Growth delay",
                        "Abnormality of body height",
                        "bone element phenotype",
                        "Abnormal mandible morphology",
                        "mandible phenotype",
                        "digit phenotype",
                        "neural fold",
                        "digit morphology phenotype",
                        "decreased length of multicellular anatomical structure",
                        "appendage phenotype",
                        "Abnormality of the integument",
                        "abdomen element phenotype",
                        "limb segment phenotype",
                        "endochondral element phenotype",
                        "absent anatomical entity in the limb",
                        "decreased size of the anatomical structure",
                        "skeleton of manus",
                        "manual digit",
                        "primary subdivision of cranial skeletal system phenotype",
                        "endochondral bone",
                        "Aplasia/Hypoplasia involving bones of the skull",
                        "limb segment",
                        "Abnormality of limb bone",
                        "arm",
                        "macromolecule biosynthetic process phenotype",
                        "autopodial skeleton",
                        "decreased size of the anatomical entity",
                        "anatomical entity physiology phenotype",
                        "programmed DNA elimination by chromosome breakage phenotype",
                        "decreased length of anatomical structure",
                        "limb bud phenotype",
                        "Aplasia/hypoplasia involving bones of the upper limbs",
                        "ecto-epithelium phenotype",
                        "face morphology phenotype",
                        "autopodial extension",
                        "forelimb zeugopod morphology phenotype",
                        "Abnormal thumb morphology",
                        "forelimb morphology phenotype",
                        "mesenchyme morphology phenotype",
                        "lateral plate mesoderm phenotype",
                        "Decreased head circumference",
                        "tissue phenotype",
                        "Short finger",
                        "manus phenotype",
                        "sensory perception of mechanical stimulus phenotype",
                        "Short thumb",
                        "anatomical entity morphology in the manus phenotype",
                        "external ectoderm",
                        "Abnormal appendicular skeleton morphology",
                        "manual digit morphology in the manus phenotype",
                        "Abnormal digit morphology",
                        "embryonic autopod plate",
                        "ocular adnexa phenotype",
                        "pectoral complex",
                        "decreased size of the anatomical conduit",
                        "limb",
                        "Abnormal hand morphology",
                        "autopod region morphology phenotype",
                        "organ system subdivision phenotype",
                        "increased size of the anatomical entity",
                        "lateral plate mesoderm morphology phenotype",
                        "decreased size of the manual digit",
                        "arm phenotype",
                        "bone of free limb or fin",
                        "decreased length of limb endochondral element",
                        "Abnormality of head or neck",
                        "limb bone",
                        "segment of autopod",
                        "external ectoderm morphology phenotype",
                        "increased biological_process in skin of body",
                        "aplasia or hypoplasia of manual digit",
                        "skeleton of limb phenotype",
                        "forelimb bud phenotype",
                        "surface structure phenotype",
                        "decreased size of the digit",
                        "organ phenotype",
                        "manual digit 1 or 5",
                        "subdivision of organism along appendicular axis phenotype",
                        "anatomical entity morphology in the appendage girdle complex phenotype",
                        "biological_process rate phenotype",
                        "Abnormal forearm morphology",
                        "system",
                        "limb bone phenotype",
                        "biological_process",
                        "multi-limb segment region phenotype",
                        "manual digit 1 plus metapodial segment",
                        "upper limb segment",
                        "decreased length of autopodial extension",
                        "segment of manus",
                        "nose tip",
                        "renal system phenotype",
                        "ectoderm morphology phenotype",
                        "manus",
                        "telencephalon",
                        "Anemia",
                        "tube",
                        "cranial skeletal system phenotype",
                        "digitopodium region",
                        "neural tube",
                        "acropodium region",
                        "decreased size of the bone of free limb or fin",
                        "ear phenotype",
                        "autopod region phenotype",
                        "decreased height of the anatomical entity",
                        "regulation of metabolic process",
                        "aplasia or hypoplasia of manual digit 1",
                        "localised abdomen element",
                        "occurrent",
                        "limb morphology phenotype",
                        "immaterial entity",
                        "skeleton of pectoral complex",
                        "decreased size of the limb bone",
                        "cranial skeletal system",
                        "appendicular skeleton",
                        "forelimb phenotype",
                        "macromolecule biosynthetic process",
                        "neural crest-derived structure phenotype",
                        "mesoderm",
                        "appendicular skeleton morphology phenotype",
                        "vestibulo-auditory system",
                        "erythrocyte morphology phenotype",
                        "Aplasia/hypoplasia involving bones of the extremities",
                        "mesoderm morphology phenotype",
                        "decreased size of the multicellular anatomical structure",
                        "decreased length of bone of free limb or fin",
                        "decreased size of the material anatomical entity",
                        "Aplasia/hypoplasia involving bones of the hand",
                        "mesenchyme phenotype",
                        "negative regulation of biological process",
                        "decreased length of digit",
                        "reproductive organ",
                        "pectoral appendage skeleton phenotype",
                        "Aplasia/hypoplasia of the extremities",
                        "Abnormality of the hand",
                        "nose tip morphology phenotype",
                        "appendicular skeletal system",
                        "external male genitalia phenotype",
                        "Abnormal skin morphology",
                        "limb bud morphology phenotype",
                        "skeleton of limb",
                        "dense mesenchyme tissue",
                        "digit",
                        "delayed biological_process",
                        "Abnormal skeletal morphology",
                        "external soft tissue zone phenotype",
                        "ectodermal placode",
                        "localised compound organ",
                        "sense organ",
                        "metabolic process",
                        "primordium phenotype",
                        "blood cell",
                        "Abnormality of the face",
                        "head bone",
                        "increased size of the olfactory organ",
                        "Abnormal nasal morphology",
                        "manual digit 1 morphology phenotype",
                        "non-neural ectoderm",
                        "decreased size of the orifice",
                        "nose",
                        "digestive system element",
                        "dermatocranium phenotype",
                        "Abnormal nasal tip morphology",
                        "limb phenotype",
                        "external nose phenotype",
                        "Bulbous nose",
                        "forelimb zeugopod phenotype",
                        "mouth morphology phenotype",
                        "limb endochondral element phenotype",
                        "olfactory organ",
                        "olfactory placode phenotype",
                        "entity",
                        "immaterial anatomical entity phenotype",
                        "neural fold morphology phenotype",
                        "increased volume of nose",
                        "nose morphology phenotype",
                        "nervous system process",
                        "increased size of the multicellular anatomical structure",
                        "cell phenotype",
                        "Abnormality of the urinary system",
                        "cranial placode phenotype",
                        "brain phenotype",
                        "external nose morphology phenotype",
                        "unilaminar epithelium phenotype",
                        "manual digitopodium region",
                        "Abnormal external nose morphology",
                        "increased size of the material anatomical entity",
                        "nose phenotype",
                        "entire sense organ system",
                        "forelimb long bone phenotype",
                        "renal system morphology phenotype",
                        "olfactory placode",
                        "Abnormal male external genitalia morphology",
                        "increased biological_process",
                        "endochondral bone phenotype",
                        "non-neural ectoderm phenotype",
                        "localised material anatomical entity",
                        "primordium",
                        "embryo",
                        "Localized skin lesion",
                        "skin of body morphology phenotype",
                        "skin of body phenotype",
                        "increased pigmentation",
                        "Abnormal reproductive system morphology",
                        "increased qualitatively biological_process",
                        "future central nervous system",
                        "Abnormality of skin pigmentation",
                        "Irregular hyperpigmentation",
                        "forelimb zeugopod bone morphology phenotype",
                        "integument",
                        "skin of body",
                        "anatomical entity morphology in the skeleton of pectoral complex phenotype",
                        "ectoderm-derived structure phenotype",
                        "integumental system",
                        "embryonic facial prominence",
                        "blood cell phenotype",
                        "epithelial fold",
                        "eye primordium",
                    ],
                    "highlighting": None,
                },
                {
                    "id": "MONDO:0024525",
                    "category": "biolink:Disease",
                    "name": "Fanconi renotubular syndrome 1",
                    "provided_by": "phenio_nodes",
                    "xref": ["DOID:0080757", "MEDGEN:1635492", "OMIM:134600", "UMLS:C4551503"],
                    "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",
                    ],
                    "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"
                    ],
                    "subsets": ["gard_rare", "nord_rare", "otar", "rare"],
                    "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_count": 16,
                    "has_phenotype_closure": [
                        "HP:0000083",
                        "HP:0001324",
                        "UPHENO:0002359",
                        "HP:0003011",
                        "UPHENO:0003047",
                        "UPHENO:0002320",
                        "CHEBI:33839",
                        "HP:0000093",
                        "CHEBI:32988",
                        "CHEBI:16541",
                        "CHEBI:16670",
                        "CHEBI:33256",
                        "CHEBI:37622",
                        "HP:0020129",
                        "UPHENO:0081423",
                        "UPHENO:0069254",
                        "HP:0001507",
                        "HP:0004322",
                        "UPHENO:0080352",
                        "UPHENO:0081424",
                        "UPHENO:0069062",
                        "HP:0001510",
                        "UPHENO:0003022",
                        "UPHENO:0075195",
                        "UPHENO:0080351",
                        "UPHENO:0068971",
                        "CHEBI:15841",
                        "UPHENO:0000541",
                        "UPHENO:0049874",
                        "UPHENO:0069327",
                        "UPHENO:0068491",
                        "CHEBI:33608",
                        "UPHENO:0080556",
                        "UPHENO:0068565",
                        "CHEBI:24651",
                        "CHEBI:72695",
                        "CHEBI:64709",
                        "CHEBI:35605",
                        "CHEBI:36586",
                        "CHEBI:36587",
                        "CHEBI:33575",
                        "HP:0025745",
                        "UPHENO:0081777",
                        "PR:000003968",
                        "HP:0004379",
                        "UPHENO:0075666",
                        "UPHENO:0075159",
                        "CHEBI:35352",
                        "HP:0003155",
                        "PR:000018263",
                        "PR:000000001",
                        "HP:0034684",
                        "CHEBI:17234",
                        "CHEBI:33917",
                        "CHEBI:15693",
                        "CHEBI:18133",
                        "CHEBI:35381",
                        "CHEBI:33304",
                        "UPHENO:0080658",
                        "HP:6000531",
                        "CHEBI:36963",
                        "CHEBI:33285",
                        "CHEBI:33582",
                        "CHEBI:36962",
                        "CHEBI:25806",
                        "CHEBI:16646",
                        "HP:0003355",
                        "CHEBI:78616",
                        "UPHENO:0068054",
                        "UBERON:0005090",
                        "HP:0003126",
                        "HP:0003076",
                        "GO:0003014",
                        "GO:0003008",
                        "GO:0070293",
                        "UPHENO:0051280",
                        "UPHENO:0050106",
                        "HP:0002748",
                        "UPHENO:0082834",
                        "UPHENO:0076692",
                        "GO:0032501",
                        "HP:0002749",
                        "UBERON:0001474",
                        "UBERON:0001434",
                        "UBERON:0002204",
                        "UPHENO:0084653",
                        "HP:0033127",
                        "UPHENO:0076703",
                        "UPHENO:0084654",
                        "HP:0011842",
                        "UBERON:0004765",
                        "UPHENO:0082835",
                        "UPHENO:0081581",
                        "UPHENO:0079822",
                        "UPHENO:3000004",
                        "HP:0010929",
                        "UBERON:0010000",
                        "HP:0011038",
                        "UPHENO:0002269",
                        "UBERON:0001008",
                        "UBERON:0000062",
                        "BFO:0000004",
                        "UPHENO:0066921",
                        "UBERON:0006555",
                        "UPHENO:0002636",
                        "UBERON:0001015",
                        "HP:0012599",
                        "UPHENO:0003088",
                        "HP:0011277",
                        "UPHENO:0002532",
                        "HP:0033354",
                        "UBERON:0004111",
                        "HP:0000924",
                        "UPHENO:0082875",
                        "CHEBI:36914",
                        "GO:0042592",
                        "HP:0004348",
                        "UPHENO:0002536",
                        "UPHENO:0066950",
                        "UBERON:0000174",
                        "UPHENO:0046348",
                        "UBERON:0000489",
                        "UPHENO:0002963",
                        "UBERON:0005177",
                        "BFO:0000001",
                        "UBERON:0005172",
                        "HP:0004360",
                        "UPHENO:0069266",
                        "PR:000064867",
                        "UPHENO:0002976",
                        "CHEBI:26079",
                        "CHEBI:33302",
                        "CHEBI:50047",
                        "UBERON:0000923",
                        "CHEBI:36360",
                        "UPHENO:0004459",
                        "CHEBI:22314",
                        "UBERON:0005173",
                        "UPHENO:0002541",
                        "CHEBI:26020",
                        "HP:0012211",
                        "CHEBI:24867",
                        "HP:0001941",
                        "HP:0003648",
                        "UPHENO:0002542",
                        "CHEBI:33238",
                        "UPHENO:0002668",
                        "HP:0003111",
                        "UPHENO:0003432",
                        "UBERON:0000467",
                        "UPHENO:0002525",
                        "UPHENO:0002531",
                        "UBERON:0000383",
                        "UBERON:0004120",
                        "UPHENO:0002564",
                        "CHEBI:33241",
                        "HP:0001942",
                        "UPHENO:0005092",
                        "UPHENO:0005141",
                        "UPHENO:0002530",
                        "UPHENO:0000543",
                        "HP:0000002",
                        "UPHENO:0002949",
                        "UPHENO:0003381",
                        "UBERON:0006314",
                        "UBERON:0001630",
                        "UBERON:0007688",
                        "CHEBI:33674",
                        "UBERON:0000922",
                        "HP:0000118",
                        "HP:0034359",
                        "UPHENO:0002252",
                        "HP:0032180",
                        "UPHENO:0080555",
                        "GO:0009987",
                        "HP:0001939",
                        "UBERON:0009569",
                        "UBERON:0000468",
                        "UPHENO:0046284",
                        "UBERON:0003081",
                        "BFO:0000015",
                        "UPHENO:0001003",
                        "UBERON:0007524",
                        "UBERON:0000475",
                        "UBERON:0003104",
                        "UPHENO:0005201",
                        "UPHENO:0002567",
                        "UPHENO:0002964",
                        "UPHENO:0049904",
                        "UPHENO:0051763",
                        "UPHENO:0004892",
                        "GO:0008150",
                        "UPHENO:0002422",
                        "UPHENO:0003159",
                        "UPHENO:0034522",
                        "GO:0040007",
                        "HP:0012337",
                        "UPHENO:0003093",
                        "UBERON:0005423",
                        "UPHENO:0066946",
                        "UBERON:0000465",
                        "UBERON:0000463",
                        "UBERON:0000179",
                        "UBERON:0004211",
                        "UPHENO:0002554",
                        "UBERON:0001231",
                        "CHEBI:23367",
                        "GO:0008152",
                        "CHEBI:33559",
                        "UPHENO:0052002",
                        "UPHENO:0051960",
                        "UPHENO:0024906",
                        "UPHENO:0051191",
                        "UPHENO:0001002",
                        "UPHENO:0002559",
                        "UPHENO:0002870",
                        "UPHENO:0002754",
                        "HP:0000079",
                        "UBERON:0001062",
                        "CHEBI:37577",
                        "UBERON:0004122",
                        "HP:0004349",
                        "UPHENO:0002311",
                        "CHEBI:59999",
                        "UPHENO:0005285",
                        "CHEBI:36357",
                        "UPHENO:0046383",
                        "UBERON:0000061",
                        "UPHENO:0066739",
                        "UPHENO:0002577",
                        "UBERON:0003103",
                        "HP:0100529",
                        "BFO:0000040",
                        "CHEBI:26082",
                        "UPHENO:0002411",
                        "CHEBI:33521",
                        "UBERON:0002100",
                        "UPHENO:0051709",
                        "UPHENO:0051804",
                        "UPHENO:0003050",
                        "HP:0002148",
                        "UBERON:0013702",
                        "UPHENO:0004680",
                        "UPHENO:0002816",
                        "CHEBI:24870",
                        "UPHENO:0002571",
                        "UBERON:0005291",
                        "UBERON:0000916",
                        "UBERON:0006598",
                        "UBERON:0001088",
                        "UBERON:0000178",
                        "UPHENO:0034253",
                        "UBERON:0002417",
                        "CHEBI:60242",
                        "BFO:0000003",
                        "UPHENO:0002386",
                        "UPHENO:0066959",
                        "UPHENO:0002859",
                        "UPHENO:0003025",
                        "UPHENO:0046286",
                        "UPHENO:0004505",
                        "HP:0002900",
                        "UPHENO:0051686",
                        "CHEBI:24431",
                        "UPHENO:0081547",
                        "UBERON:0000479",
                        "CHEBI:33579",
                        "UPHENO:0049587",
                        "CHEBI:28358",
                        "CHEBI:33259",
                        "UPHENO:0066960",
                        "UBERON:0003061",
                        "UPHENO:0066943",
                        "UBERON:0010316",
                        "UPHENO:0003430",
                        "UPHENO:0002210",
                        "CHEBI:51143",
                        "UPHENO:0002803",
                        "UBERON:8450002",
                        "HP:0000124",
                        "HP:0011804",
                        "UPHENO:0002832",
                        "UBERON:0011143",
                        "UBERON:0002113",
                        "UBERON:0000025",
                        "UBERON:0000926",
                        "HP:0000077",
                        "UPHENO:0002287",
                        "UPHENO:0002909",
                        "UPHENO:0003207",
                        "UPHENO:0075902",
                        "UPHENO:0002526",
                        "UPHENO:0002731",
                        "UPHENO:0002426",
                        "UPHENO:0068169",
                        "UPHENO:0002267",
                        "BFO:0000002",
                        "HP:0000119",
                        "UPHENO:0004503",
                        "UPHENO:0081544",
                        "HP:0012072",
                        "UPHENO:0002926",
                        "UPHENO:0068144",
                        "UPHENO:0066939",
                        "UPHENO:0002248",
                        "UPHENO:0002360",
                        "CHEBI:36359",
                        "UPHENO:0003941",
                        "HP:0003330",
                        "UPHENO:0001001",
                        "UPHENO:0002442",
                        "UPHENO:0051739",
                        "UPHENO:0004885",
                        "HP:0000001",
                        "UPHENO:0003094",
                        "CHEBI:25367",
                        "UPHENO:0066925",
                        "UPHENO:0068352",
                        "UPHENO:0003413",
                        "UPHENO:0066954",
                        "UPHENO:0049703",
                        "UPHENO:0048707",
                        "UPHENO:0034351",
                        "UPHENO:0066951",
                        "UPHENO:0002308",
                        "HP:0012379",
                        "UPHENO:0002427",
                        "UPHENO:0002385",
                        "UBERON:0007684",
                        "UBERON:0009773",
                        "UPHENO:0051645",
                        "HP:0011849",
                        "UPHENO:0002346",
                        "UPHENO:0004791",
                        "CHEBI:24835",
                        "UPHENO:0066927",
                        "UPHENO:0002642",
                        "CHEBI:50860",
                        "UPHENO:0002568",
                        "UPHENO:0005277",
                        "UBERON:0002390",
                        "UBERON:0011216",
                        "CHEBI:24833",
                        "UPHENO:0004360",
                        "UBERON:0000064",
                        "HP:0032943",
                        "UPHENO:0002377",
                        "HP:0010935",
                        "UPHENO:0002246",
                        "UPHENO:0066964",
                        "CHEBI:36916",
                        "UBERON:0015212",
                        "UPHENO:0004969",
                        "CHEBI:26216",
                        "UBERON:0011676",
                        "CHEBI:33709",
                        "UPHENO:0003163",
                        "UBERON:0007503",
                        "UPHENO:0034199",
                        "UBERON:0004819",
                        "UBERON:0003914",
                        "UBERON:0001285",
                        "UPHENO:0046283",
                        "UPHENO:0051900",
                        "UPHENO:0068110",
                        "HP:0003109",
                        "HP:0003110",
                        "HP:0012591",
                        "UPHENO:0068511",
                        "UBERON:0003918",
                        "UPHENO:0004418",
                        "UPHENO:0004900",
                        "CHEBI:60911",
                        "UPHENO:0066913",
                        "CHEBI:33250",
                        "CHEBI:60004",
                        "UPHENO:0089294",
                        "CHEBI:33675",
                        "UBERON:0013701",
                        "UPHENO:0076286",
                        "UBERON:0002193",
                        "UPHENO:0089770",
                        "CHEBI:33318",
                        "UPHENO:0089756",
                        "GO:0001503",
                        "UPHENO:0066903",
                        "HP:0010930",
                        "UBERON:0002050",
                        "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",
                    ],
                    "highlighting": None,
                },
                {
                    "id": "MONDO:0014985",
                    "category": "biolink:Disease",
                    "name": "Fanconi anemia complementation group V",
                    "description": "Any Fanconi anemia in which the cause of the disease is a mutation in the MAD2L2 gene.",
                    "provided_by": "phenio_nodes",
                    "xref": ["DOID:0111080", "GARD:16213", "MEDGEN:934619", "OMIM:617243", "UMLS:C4310652"],
                    "synonym": [
                        "FANCV",
                        "Fanconi Anemia, complementation Group 5",
                        "Fanconi Anemia, complementation group V",
                        "Fanconi Anemia, complementation group type V",
                        "Fanconi anaemia caused by mutation in MAD2L2",
                        "Fanconi anaemia complementation group type V",
                        "Fanconi anemia caused by mutation in MAD2L2",
                        "Fanconi anemia complementation group type V",
                        "Fanconi anemia, complementation GROUP V",
                        "MAD2L2 Fanconi anaemia",
                        "MAD2L2 Fanconi anemia",
                    ],
                    "exact_synonyms": [
                        "FANCV|Fanconi Anemia, complementation group V|Fanconi Anemia, complementation group type V|Fanconi anaemia caused by mutation in MAD2L2|Fanconi anaemia complementation group type V|Fanconi anemia caused by mutation in MAD2L2|Fanconi anemia complementation group type V|MAD2L2 Fanconi anaemia|MAD2L2 Fanconi anemia"
                    ],
                    "related_synonyms": [
                        "Fanconi Anemia, complementation Group 5|Fanconi anemia, complementation GROUP V"
                    ],
                    "subsets": ["gard_rare", "nord_rare", "rare"],
                    "namespace": "MONDO",
                    "has_phenotype": [
                        "HP:0001875",
                        "HP:0001873",
                        "HP:0005528",
                        "HP:0006254",
                        "HP:0003221",
                        "HP:0001903",
                        "HP:0004322",
                        "HP:0000252",
                    ],
                    "has_phenotype_label": [
                        "Decreased total neutrophil count",
                        "Thrombocytopenia",
                        "Bone marrow hypocellularity",
                        "Elevated circulating alpha-fetoprotein concentration",
                        "Chromosomal breakage induced by crosslinking agents",
                        "Anemia",
                        "Short stature",
                        "Microcephaly",
                    ],
                    "has_phenotype_count": 8,
                    "has_phenotype_closure": [
                        "UBERON:0011676",
                        "NCBITaxon:33208",
                        "UBERON:0001890",
                        "UBERON:0000955",
                        "UBERON:0001893",
                        "UPHENO:0087518",
                        "UPHENO:0076791",
                        "UPHENO:0004704",
                        "UPHENO:0087661",
                        "HP:0002060",
                        "UBERON:0010314",
                        "UPHENO:0002553",
                        "UPHENO:0004802",
                        "UPHENO:0004615",
                        "HP:0000929",
                        "UBERON:0006601",
                        "UPHENO:0002548",
                        "UPHENO:0002859",
                        "UPHENO:0003025",
                        "UPHENO:0076805",
                        "HP:0000252",
                        "UPHENO:0080079",
                        "NCBITaxon:6072",
                        "HP:0002977",
                        "UBERON:0010912",
                        "UPHENO:0005141",
                        "UBERON:0034925",
                        "UPHENO:0005092",
                        "UPHENO:0075804",
                        "HP:0012443",
                        "UPHENO:0002816",
                        "NCBITaxon:33154",
                        "UPHENO:0005285",
                        "UBERON:0007811",
                        "UPHENO:0004621",
                        "HP:0000234",
                        "HP:0100547",
                        "UBERON:0010323",
                        "UBERON:0011138",
                        "UBERON:0003129",
                        "UBERON:0011137",
                        "HP:0000707",
                        "HP:0033127",
                        "HP:0009121",
                        "NCBITaxon:1",
                        "HP:0002011",
                        "UPHENO:0076703",
                        "UPHENO:0002526",
                        "UBERON:0001049",
                        "UBERON:0003075",
                        "UBERON:0003080",
                        "HP:0000152",
                        "UBERON:0016879",
                        "NCBITaxon:2759",
                        "HP:0011842",
                        "UPHENO:0086485",
                        "UBERON:0000153",
                        "UBERON:0004288",
                        "UPHENO:0003004",
                        "UBERON:0000924",
                        "UPHENO:0002736",
                        "UBERON:0003056",
                        "UPHENO:0004484",
                        "UBERON:0004111",
                        "UPHENO:0076799",
                        "UBERON:0004734",
                        "UBERON:0000475",
                        "UPHENO:0005055",
                        "UPHENO:0086589",
                        "UPHENO:0087660",
                        "UBERON:0003061",
                        "UPHENO:0004523",
                        "UPHENO:0051804",
                        "CL:0000988",
                        "UPHENO:0048707",
                        "UPHENO:0051612",
                        "UBERON:0001015",
                        "UPHENO:0004888",
                        "HP:0011873",
                        "UPHENO:0002844",
                        "UBERON:0001434",
                        "GO:0019222",
                        "UPHENO:0003177",
                        "UPHENO:0003207",
                        "UPHENO:0080200",
                        "BFO:0000003",
                        "HP:0011017",
                        "UPHENO:0087907",
                        "UPHENO:0004503",
                        "UPHENO:0004519",
                        "HP:0032309",
                        "UPHENO:0077373",
                        "UPHENO:0088170",
                        "UPHENO:0004892",
                        "UPHENO:0002964",
                        "UPHENO:0049904",
                        "UPHENO:0051763",
                        "HP:0012145",
                        "CL:0000457",
                        "UPHENO:0002536",
                        "GO:0010558",
                        "UBERON:0002204",
                        "CL:0000151",
                        "NCBITaxon:131567",
                        "UBERON:0002090",
                        "CL:0000763",
                        "UPHENO:0003163",
                        "GO:0040007",
                        "UBERON:0004765",
                        "UPHENO:0081566",
                        "HP:0011875",
                        "UPHENO:0002564",
                        "BFO:0000004",
                        "UBERON:0003104",
                        "GO:0009059",
                        "UBERON:0001474",
                        "UPHENO:0086173",
                        "HP:0001873",
                        "CL:0000458",
                        "HP:0001507",
                        "HP:0001872",
                        "UPHENO:0087123",
                        "UPHENO:0081581",
                        "UBERON:0016880",
                        "UPHENO:0088176",
                        "HP:0001911",
                        "UPHENO:0052002",
                        "UPHENO:0003186",
                        "CL:0000775",
                        "UPHENO:0080010",
                        "HP:0001874",
                        "UPHENO:0002948",
                        "UBERON:0013702",
                        "UPHENO:0004680",
                        "UPHENO:0076675",
                        "BFO:0000002",
                        "CHEBI:16541",
                        "HP:0045056",
                        "UBERON:0000073",
                        "UBERON:0002405",
                        "UPHENO:0077826",
                        "HP:0012639",
                        "CHEBI:33302",
                        "HP:0001510",
                        "CL:0000738",
                        "UPHENO:0085344",
                        "UBERON:0010000",
                        "HP:0032251",
                        "CL:0000000",
                        "CHEBI:51143",
                        "CL:0000766",
                        "UPHENO:0085371",
                        "UBERON:0004121",
                        "UBERON:0000062",
                        "UPHENO:0011498",
                        "UBERON:0000483",
                        "UBERON:0002050",
                        "UBERON:0001016",
                        "UPHENO:0001001",
                        "UBERON:0000465",
                        "CHEBI:33304",
                        "UBERON:0005944",
                        "UBERON:0005423",
                        "UBERON:0000481",
                        "HP:0007364",
                        "UPHENO:0004521",
                        "UPHENO:0086019",
                        "UBERON:0001062",
                        "UPHENO:0077391",
                        "UPHENO:0088123",
                        "CL:0000255",
                        "CL:0000219",
                        "GO:0010467",
                        "UPHENO:0086176",
                        "UPHENO:0085330",
                        "CL:0000094",
                        "UBERON:0015203",
                        "UPHENO:0003159",
                        "GO:0060255",
                        "UBERON:0002346",
                        "UPHENO:0063787",
                        "UBERON:0000383",
                        "UBERON:0004120",
                        "UPHENO:0002926",
                        "UPHENO:0063794",
                        "UPHENO:0087363",
                        "PR:000018263",
                        "HP:0001881",
                        "UBERON:0000479",
                        "CHEBI:33579",
                        "UPHENO:0003236",
                        "UBERON:0000075",
                        "HP:0001903",
                        "UPHENO:0002668",
                        "HP:0001871",
                        "UBERON:0011216",
                        "UBERON:0002390",
                        "UPHENO:0086172",
                        "GO:0008150",
                        "UPHENO:0004459",
                        "UPHENO:0077399",
                        "UBERON:0000468",
                        "UPHENO:0075195",
                        "HP:0010987",
                        "HP:0011991",
                        "GO:0050794",
                        "BFO:0000001",
                        "UPHENO:3000000",
                        "UPHENO:0002530",
                        "UPHENO:0086016",
                        "UBERON:0002193",
                        "CL:0000233",
                        "UPHENO:0087665",
                        "UPHENO:0003432",
                        "UBERON:0000467",
                        "UPHENO:0002525",
                        "UBERON:0002371",
                        "UPHENO:0001003",
                        "UPHENO:0088166",
                        "UPHENO:0001002",
                        "UPHENO:0006894",
                        "UPHENO:0085302",
                        "HP:0011893",
                        "CL:0000081",
                        "UBERON:0007524",
                        "UPHENO:0077418",
                        "UPHENO:0003001",
                        "UPHENO:0049587",
                        "HP:0010974",
                        "BFO:0000040",
                        "UPHENO:0085356",
                        "UPHENO:0049835",
                        "UPHENO:0077348",
                        "HP:0002715",
                        "CL:0000225",
                        "UBERON:0003914",
                        "HP:0001875",
                        "UPHENO:0085354",
                        "UBERON:0034923",
                        "UBERON:0003081",
                        "CL:0002242",
                        "UPHENO:0002963",
                        "UBERON:0010316",
                        "UPHENO:0002554",
                        "UBERON:0000179",
                        "UPHENO:0002902",
                        "UBERON:0000463",
                        "HP:0000924",
                        "GO:0042592",
                        "HP:0000118",
                        "UBERON:0000922",
                        "GO:0009058",
                        "GO:0048519",
                        "UBERON:0013701",
                        "UPHENO:0076286",
                        "CHEBI:33675",
                        "UPHENO:0004505",
                        "UBERON:0010371",
                        "PR:000000001",
                        "HP:0000001",
                        "UPHENO:0004885",
                        "UBERON:0006598",
                        "HP:0005528",
                        "CHEBI:37622",
                        "CL:0001035",
                        "HP:0010876",
                        "UBERON:0000923",
                        "CHEBI:50047",
                        "CHEBI:33256",
                        "CHEBI:16670",
                        "CHEBI:36357",
                        "UPHENO:0049870",
                        "HP:0001877",
                        "UPHENO:0002542",
                        "CHEBI:33839",
                        "UBERON:0001017",
                        "UPHENO:0002568",
                        "CHEBI:50860",
                        "CL:0002092",
                        "GO:0031052",
                        "UPHENO:0076702",
                        "CHEBI:25806",
                        "UPHENO:0002567",
                        "UPHENO:0002976",
                        "PR:000064867",
                        "UPHENO:0069266",
                        "UPHENO:0002764",
                        "UBERON:0000061",
                        "UPHENO:0046383",
                        "HP:0001939",
                        "CHEBI:23367",
                        "GO:0008152",
                        "UPHENO:0049652",
                        "UPHENO:0046284",
                        "UPHENO:0089759",
                        "UPHENO:0050121",
                        "HP:0040195",
                        "UBERON:0000025",
                        "UPHENO:0088162",
                        "UBERON:0005291",
                        "UPHENO:0002571",
                        "CHEBI:32988",
                        "CHEBI:33285",
                        "UPHENO:0011531",
                        "UPHENO:0050007",
                        "CL:0000764",
                        "UPHENO:0075220",
                        "CHEBI:36963",
                        "HP:0003220",
                        "UPHENO:0077817",
                        "UPHENO:0002541",
                        "BFO:0000015",
                        "UPHENO:0089764",
                        "UPHENO:0048751",
                        "HP:0032180",
                        "HP:0006254",
                        "UPHENO:0011536",
                        "UPHENO:0069062",
                        "UPHENO:0004900",
                        "UPHENO:0004418",
                        "UPHENO:0000541",
                        "CHEBI:15841",
                        "UPHENO:0086679",
                        "CHEBI:36962",
                        "UPHENO:0077822",
                        "CHEBI:33582",
                        "PR:000003809",
                        "UPHENO:0081547",
                        "CHEBI:24431",
                        "GO:0009987",
                        "UPHENO:0046378",
                        "UBERON:0000178",
                        "HP:0003221",
                        "UPHENO:0049873",
                        "UPHENO:0068971",
                        "UPHENO:0049837",
                        "HP:0000240",
                        "UPHENO:0002577",
                        "UPHENO:0078606",
                        "UPHENO:0076692",
                        "GO:0005623",
                        "GO:0048523",
                        "GO:0010629",
                        "GO:0031049",
                        "HP:0040012",
                        "UPHENO:0081424",
                        "UBERON:0000033",
                        "UBERON:0000926",
                        "GO:0010605",
                        "GO:0009890",
                        "GO:0010556",
                        "GO:0043170",
                        "GO:0010468",
                        "UPHENO:0002532",
                        "GO:0050789",
                        "UPHENO:0080351",
                        "HP:0005561",
                        "GO:0009892",
                        "UBERON:0002616",
                        "GO:0009889",
                        "HP:0025354",
                        "GO:0065007",
                        "UPHENO:0063722",
                        "UPHENO:0050065",
                        "CL:0000329",
                        "UPHENO:0005030",
                        "UBERON:0000307",
                        "CL:0000232",
                        "UPHENO:0069327",
                        "UPHENO:0000543",
                        "UBERON:0006314",
                        "UPHENO:0002949",
                        "HP:0000002",
                        "UPHENO:0049874",
                        "CHEBI:35352",
                        "UPHENO:0075159",
                        "UPHENO:0080352",
                        "HP:0004322",
                        "UPHENO:0069254",
                        "UPHENO:0081423",
                        "UPHENO:0002746",
                    ],
                    "has_phenotype_closure_label": [
                        "root",
                        "gastrula morphology phenotype",
                        "Abnormal skull morphology",
                        "Decreased head circumference",
                        "gastrula",
                        "blastula",
                        "embryonic tissue morphology phenotype",
                        "Abnormal skeletal morphology",
                        "nervous system phenotype",
                        "aplasia or hypoplasia of telencephalon",
                        "multi-tissue structure phenotype",
                        "Aplasia/Hypoplasia involving the central nervous system",
                        "epithelium",
                        "head phenotype",
                        "axial skeleton plus cranial skeleton",
                        "cranial skeletal system",
                        "postcranial axial skeletal system",
                        "skull",
                        "subdivision of skeleton",
                        "pre-chordal neural plate",
                        "musculature",
                        "subdivision of skeletal system",
                        "telencephalon morphology phenotype",
                        "neural plate phenotype",
                        "Metazoa",
                        "epithelium phenotype",
                        "tube",
                        "ectoderm morphology phenotype",
                        "regional part of nervous system",
                        "musculature of body phenotype",
                        "central nervous system phenotype",
                        "regional part of brain",
                        "neural tube morphology phenotype",
                        "forebrain morphology phenotype",
                        "tube phenotype",
                        "body proper",
                        "craniocervical region",
                        "presumptive ectoderm phenotype",
                        "neurectoderm",
                        "Abnormal cerebral morphology",
                        "Eukaryota",
                        "neurectoderm phenotype",
                        "ectoderm",
                        "neural plate morphology phenotype",
                        "craniofacial/craniocervical phenotype",
                        "future nervous system",
                        "brain phenotype",
                        "Abnormal axial skeleton morphology",
                        "embryo morphology phenotype",
                        "epithelial tube",
                        "main body axis",
                        "subdivision of organism along main body axis",
                        "central nervous system morphology phenotype",
                        "structure with developmental contribution from neural crest",
                        "multi-tissue structure",
                        "skeletal system phenotype",
                        "Morphological central nervous system abnormality",
                        "nervous system",
                        "forebrain phenotype",
                        "Abnormal nervous system morphology",
                        "central nervous system",
                        "organ phenotype",
                        "anterior neural tube phenotype",
                        "Abnormality of the musculoskeletal system",
                        "subdivision of organism along main body axis phenotype",
                        "regional part of nervous system phenotype",
                        "organism subdivision phenotype",
                        "homeostatic process",
                        "blood organic amino compound level phenotype",
                        "mesenchyme phenotype",
                        "Abnormality of skull size",
                        "presumptive ectoderm",
                        "dense mesenchyme tissue phenotype",
                        "ecto-epithelium phenotype",
                        "phenotype",
                        "structure with developmental contribution from neural crest phenotype",
                        "molecular entity",
                        "bodily fluid phenotype",
                        "pnictogen molecular entity",
                        "protein-containing molecular entity",
                        "polypeptide",
                        "Abnormal circulating protein concentration",
                        "organ",
                        "haemolymphatic fluid phenotype",
                        "bone marrow cell",
                        "myeloid leukocyte",
                        "tissue",
                        "head",
                        "musculature of body",
                        "organ system subdivision phenotype",
                        "neural tube phenotype",
                        "Bone marrow hypocellularity",
                        "ectoderm-derived structure phenotype",
                        "Abnormal bone marrow cell morphology",
                        "Opisthokonta",
                        "motile cell",
                        "epithelial tube phenotype",
                        "musculoskeletal system",
                        "bone element",
                        "regulation of biosynthetic process",
                        "blood protein polypeptide chain level phenotype",
                        "Abnormality of multiple cell lineages in the bone marrow",
                        "Elevated circulating alpha-fetoprotein concentration",
                        "platelet",
                        "myeloid cell",
                        "decreased number of anatomical structure",
                        "bone marrow",
                        "macromolecule biosynthetic process",
                        "neutrophil phenotype",
                        "independent continuant",
                        "Abnormal platelet morphology",
                        "decreased height of the multicellular organism",
                        "future central nervous system",
                        "leukocyte morphology phenotype",
                        "anatomical system",
                        "craniocervical region morphology phenotype",
                        "skeletal system",
                        "Abnormal circulating metabolite concentration",
                        "nitrogen molecular entity",
                        "obsolete cell",
                        "mesoderm-derived structure phenotype",
                        "decreased number of hematopoietic cell",
                        "disconnected anatomical group",
                        "skeletal element",
                        "heteroorganic entity",
                        "Abnormal leukocyte count",
                        "anatomical structure",
                        "number of leukocyte phenotype",
                        "negative regulation of gene expression phenotype",
                        "telencephalon phenotype",
                        "Abnormality of the immune system",
                        "oxygen molecular entity",
                        "number of myeloid cell phenotype",
                        "ectoderm phenotype",
                        "material anatomical entity phenotype",
                        "cell phenotype",
                        "decreased size of the multicellular organism",
                        "material anatomical entity",
                        "anatomical entity phenotype",
                        "presumptive structure",
                        "Abnormal total neutrophil count",
                        "germ layer phenotype",
                        "embryonic structure phenotype",
                        "Abnormal brain morphology",
                        "Chromosomal breakage induced by crosslinking agents",
                        "alpha-fetoprotein level phenotype",
                        "anatomical system phenotype",
                        "anatomical entity morphology phenotype",
                        "decreased number of granulocyte",
                        "number of anatomical enitites of type neutrophil phenotype",
                        "Aplasia/Hypoplasia of the cerebrum",
                        "multicellular organism morphology phenotype",
                        "decreased size of the anatomical entity",
                        "number of anatomical enitites of type anatomical entity phenotype",
                        "Abnormality of the nervous system",
                        "multicellular anatomical structure",
                        "subdivision of skeletal system phenotype",
                        "growth phenotype",
                        "organism substance",
                        "ecto-epithelium",
                        "number of cell phenotype",
                        "myeloid leukocyte phenotype",
                        "dense mesenchyme tissue",
                        "germ layer / neural crest",
                        "eukaryotic cell",
                        "regulation of metabolic process",
                        "serotonin secreting cell",
                        "Microcephaly",
                        "embryo phenotype",
                        "Abnormality of thrombocytes",
                        "Thrombocytopenia",
                        "mesoderm-derived structure",
                        "Abnormal immune system morphology",
                        "organic molecular entity",
                        "gene expression",
                        "continuant",
                        "Abnormal cellular immune system morphology",
                        "Abnormality of neutrophils",
                        "multicellular anatomical structure phenotype",
                        "peptide",
                        "decreased size of the multicellular anatomical structure",
                        "metabolic process",
                        "haemolymphatic fluid",
                        "Abnormal forebrain morphology",
                        "number of anatomical enitites of type material anatomical entity phenotype",
                        "Abnormal erythrocyte morphology",
                        "Phenotypic abnormality",
                        "hematopoietic system",
                        "non-connected functional system",
                        "brain",
                        "mesenchyme",
                        "immune system morphology phenotype",
                        "Anemia",
                        "alpha-fetoprotein",
                        "p-block molecular entity",
                        "platelet phenotype",
                        "regional part of brain phenotype",
                        "regulation of gene expression",
                        "Abnormal myeloid leukocyte morphology",
                        "amide",
                        "Growth delay",
                        "Abnormal granulocyte morphology",
                        "organic amino compound",
                        "biogenic amine secreting cell",
                        "blood chemical entity level phenotype",
                        "hematopoietic cell",
                        "germ layer morphology phenotype",
                        "Abnormality of chromosome stability",
                        "future central nervous system phenotype",
                        "decreased number of material anatomical entity",
                        "blood cell",
                        "Abnormality of blood and blood-forming tissues",
                        "negative regulation of biological process",
                        "postcranial axial skeleton",
                        "anatomical conduit",
                        "metabolic process phenotype",
                        "aplasia or hypoplasia of anatomical entity",
                        "musculoskeletal system phenotype",
                        "organ system subdivision",
                        "organochalcogen compound",
                        "number of anatomical enitites of type anatomical structure phenotype",
                        "carbon group molecular entity",
                        "hemolymphoid system",
                        "embryonic tissue phenotype",
                        "taxon specific phenotype",
                        "secretory cell",
                        "cranial skeletal system phenotype",
                        "cellular process phenotype",
                        "decreased size of the anatomical structure",
                        "axial skeletal system",
                        "nervous system morphology phenotype",
                        "multicellular organism",
                        "Abnormality of the head",
                        "Abnormality of metabolism/homeostasis",
                        "protein polypeptide chain",
                        "granulocyte",
                        "neutrophil",
                        "decreased number of myeloid cell",
                        "leukocyte",
                        "erythrocyte morphology phenotype",
                        "Abnormal platelet count",
                        "Eumetazoa",
                        "immune system phenotype",
                        "neural plate",
                        "Abnormality of body height",
                        "bone cell",
                        "decreased number of cell",
                        "decreased number of anatomical entity",
                        "regulation of biological process",
                        "skull morphology phenotype",
                        "chalcogen molecular entity",
                        "material entity",
                        "organooxygen compound",
                        "number of hematopoietic cell phenotype",
                        "Abnormal granulocyte count",
                        "number of platelet phenotype",
                        "Abnormality of head or neck",
                        "granulocyte morphology phenotype",
                        "anatomical structure phenotype",
                        "Abnormality of the skeletal system",
                        "hematopoietic system phenotype",
                        "musculature phenotype",
                        "negative regulation of cellular process",
                        "immune system",
                        "embryonic structure",
                        "tissue phenotype",
                        "craniocervical region phenotype",
                        "oxygen accumulating cell",
                        "tissue chemical entity level phenotype",
                        "phenotypic effect",
                        "developing anatomical structure",
                        "carboxamide",
                        "amino acid chain",
                        "size of multicellular organism phenotype",
                        "skeleton",
                        "presumptive structure phenotype",
                        "blood island",
                        "anterior region of body",
                        "protein",
                        "lateral plate mesoderm phenotype",
                        "decreased number of neutrophil",
                        "chemical entity level phenotype",
                        "anterior neural tube",
                        "biological_process",
                        "neural tube",
                        "Abnormal circulating alpha-fetoprotein concentration",
                        "polyatomic entity",
                        "Chromosome breakage",
                        "decreased number of leukocyte",
                        "entity",
                        "growth",
                        "main group molecular entity",
                        "developing anatomical structure phenotype",
                        "blood organic molecular entity level phenotype",
                        "role blood level phenotype",
                        "negative regulation of macromolecule metabolic process",
                        "increased level of chemical entity",
                        "decreased number of platelet",
                        "blood island phenotype",
                        "embryo",
                        "erythrocyte",
                        "decreased height of the anatomical entity",
                        "macromolecule",
                        "occurrent",
                        "chemical entity",
                        "cellular process",
                        "size of skull phenotype",
                        "anatomical collection",
                        "increased level of alpha-fetoprotein",
                        "blood phenotype",
                        "All",
                        "mesoderm phenotype",
                        "role bodily fluid level phenotype",
                        "forebrain",
                        "blood nitrogen molecular entity level phenotype",
                        "Abnormal leukocyte morphology",
                        "homeostatic process phenotype",
                        "skull phenotype",
                        "gene expression phenotype",
                        "anatomical conduit phenotype",
                        "organism substance phenotype",
                        "lateral plate mesoderm",
                        "organonitrogen compound",
                        "mesoderm",
                        "Decreased total neutrophil count",
                        "germ layer / neural crest phenotype",
                        "negative regulation of biosynthetic process",
                        "regulation of cellular process",
                        "skeletal system morphology phenotype",
                        "blood oxygen molecular entity level phenotype",
                        "blood alpha-fetoprotein level phenotype",
                        "biosynthetic process phenotype",
                        "blood",
                        "embryonic tissue",
                        "process",
                        "delayed biological_process",
                        "multicellular organism chemical entity level phenotype",
                        "nitrogen molecular entity level phenotype",
                        "head morphology phenotype",
                        "ectoderm-derived structure",
                        "biological_process phenotype",
                        "blood cell phenotype",
                        "bodily fluid",
                        "negative regulation of metabolic process",
                        "number of anatomical enitites of type granulocyte phenotype",
                        "regulation of macromolecule metabolic process",
                        "regulation of macromolecule biosynthetic process",
                        "primary amide",
                        "biological regulation",
                        "germ layer",
                        "erythroid lineage cell",
                        "cellular organisms",
                        "macromolecule metabolic process",
                        "macromolecule biosynthetic process phenotype",
                        "biosynthetic process",
                        "negative regulation of gene expression",
                        "Abnormal cellular phenotype",
                        "negative regulation of macromolecule biosynthetic process",
                        "pre-chordal neural plate phenotype",
                        "delayed growth",
                        "telencephalon",
                        "macromolecule metabolic process phenotype",
                        "programmed DNA elimination by chromosome breakage phenotype",
                        "programmed DNA elimination",
                        "biological regulation phenotype",
                        "brain morphology phenotype",
                        "anucleate cell",
                        "programmed DNA elimination by chromosome breakage",
                        "erythroid lineage cell morphology phenotype",
                        "multicellular organism height phenotype",
                        "anatomical entity",
                        "size of anatomical entity phenotype",
                        "organism subdivision",
                        "anatomical entity height phenotype",
                        "nucleate cell",
                        "Short stature",
                        "multicellular organism phenotype",
                        "Growth abnormality",
                        "cell",
                        "Abnormal cellular physiology",
                        "decreased size of the material anatomical entity",
                    ],
                    "highlighting": None,
                },
                {
                    "id": "MONDO:0014986",
                    "category": "biolink:Disease",
                    "name": "Fanconi anemia complementation group R",
                    "description": "Any Fanconi anemia in which the cause of the disease is a mutation in the RAD51 gene.",
                    "provided_by": "phenio_nodes",
                    "xref": ["DOID:0111090", "GARD:16214", "MEDGEN:924579", "OMIM:617244", "UMLS:C4284093"],
                    "synonym": [
                        "FANCR",
                        "Fanconi Anemia, complementation group R",
                        "Fanconi Anemia, complementation group type R",
                        "Fanconi anaemia caused by mutation in RAD51",
                        "Fanconi anaemia complementation group type R",
                        "Fanconi anemia caused by mutation in RAD51",
                        "Fanconi anemia complementation group type R",
                        "Fanconi anemia, complementation GROUP R",
                        "RAD51 Fanconi anaemia",
                        "RAD51 Fanconi anemia",
                    ],
                    "exact_synonyms": [
                        "FANCR|Fanconi Anemia, complementation group R|Fanconi Anemia, complementation group type R|Fanconi anaemia caused by mutation in RAD51|Fanconi anaemia complementation group type R|Fanconi anemia caused by mutation in RAD51|Fanconi anemia complementation group type R|RAD51 Fanconi anaemia|RAD51 Fanconi anemia"
                    ],
                    "related_synonyms": ["Fanconi anemia, complementation GROUP R"],
                    "subsets": ["gard_rare", "nord_rare", "rare"],
                    "namespace": "MONDO",
                    "has_phenotype": [
                        "HP:0006349",
                        "HP:0001249",
                        "HP:0001510",
                        "HP:0000125",
                        "HP:0005528",
                        "HP:0006433",
                        "HP:0009777",
                        "HP:0000568",
                        "HP:0000238",
                        "HP:0007099",
                        "HP:0001903",
                        "HP:0003221",
                        "HP:0031936",
                        "HP:0002144",
                        "HP:0002650",
                        "HP:0002023",
                        "HP:0003764",
                        "HP:0000252",
                    ],
                    "has_phenotype_label": [
                        "Agenesis of permanent teeth",
                        "Intellectual disability",
                        "Growth delay",
                        "Pelvic kidney",
                        "Bone marrow hypocellularity",
                        "Radial dysplasia",
                        "Absent thumb",
                        "Microphthalmia",
                        "Hydrocephalus",
                        "Chiari type I malformation",
                        "Anemia",
                        "Chromosomal breakage induced by crosslinking agents",
                        "Delayed ability to walk",
                        "Tethered cord",
                        "Scoliosis",
                        "Anal atresia",
                        "Nevus",
                        "Microcephaly",
                    ],
                    "has_phenotype_count": 18,
                    "has_phenotype_closure": [
                        "HP:0000240",
                        "HP:0002060",
                        "UPHENO:0075804",
                        "HP:0040195",
                        "UPHENO:0081566",
                        "UPHENO:0076799",
                        "HP:0000951",
                        "HP:0011355",
                        "HP:0011121",
                        "UPHENO:0003811",
                        "UBERON:0002097",
                        "UBERON:0002199",
                        "UPHENO:0004064",
                        "UBERON:0002416",
                        "HP:0001574",
                        "UPHENO:0002812",
                        "HP:0034915",
                        "UPHENO:0086644",
                        "HP:0004378",
                        "UPHENO:0074229",
                        "HP:0002023",
                        "UBERON:0000161",
                        "UBERON:0001245",
                        "UPHENO:0074230",
                        "HP:0025031",
                        "UPHENO:0074228",
                        "UPHENO:0063562",
                        "UPHENO:0074227",
                        "UBERON:0005856",
                        "UPHENO:0002543",
                        "UPHENO:0003182",
                        "HP:0000925",
                        "UBERON:0005944",
                        "UBERON:0002090",
                        "UBERON:0001130",
                        "UPHENO:0002547",
                        "HP:0009121",
                        "UBERON:0003059",
                        "UBERON:0003077",
                        "UBERON:0007285",
                        "UBERON:0011585",
                        "UPHENO:0003234",
                        "UBERON:0007530",
                        "UBERON:0005256",
                        "UBERON:0002329",
                        "UPHENO:0004969",
                        "UPHENO:0087858",
                        "UBERON:0001137",
                        "UBERON:0005174",
                        "HP:0012758",
                        "UPHENO:0050065",
                        "HP:0003220",
                        "HP:0025354",
                        "GO:0060255",
                        "GO:0048519",
                        "GO:0043170",
                        "GO:0008152",
                        "HP:0001939",
                        "UPHENO:0050007",
                        "GO:0031049",
                        "GO:0005623",
                        "UPHENO:0078606",
                        "HP:0040012",
                        "UPHENO:0049837",
                        "HP:0003221",
                        "UPHENO:0049652",
                        "CL:0000232",
                        "UPHENO:0086172",
                        "UPHENO:0049870",
                        "CL:0000081",
                        "UPHENO:0080010",
                        "CL:0000764",
                        "HP:0001903",
                        "UPHENO:0003237",
                        "UBERON:0004733",
                        "UPHENO:0081601",
                        "UPHENO:0071325",
                        "UPHENO:0087363",
                        "UPHENO:0086932",
                        "UPHENO:0071339",
                        "HP:0007099",
                        "UPHENO:0071310",
                        "UPHENO:0075948",
                        "GO:0010629",
                        "HP:0001877",
                        "HP:0002308",
                        "UPHENO:0071315",
                        "UBERON:0003057",
                        "HP:0002438",
                        "UBERON:0004732",
                        "GO:0010468",
                        "UPHENO:0076720",
                        "UPHENO:0071344",
                        "UPHENO:0071317",
                        "UBERON:0011138",
                        "UPHENO:0003459",
                        "UPHENO:0002813",
                        "UBERON:0001895",
                        "UPHENO:0015184",
                        "UPHENO:0056230",
                        "UBERON:0000955",
                        "UPHENO:0076791",
                        "UPHENO:0076805",
                        "HP:0000238",
                        "UBERON:0004923",
                        "UBERON:0003947",
                        "UPHENO:0005029",
                        "UPHENO:0063599",
                        "UPHENO:0004418",
                        "UPHENO:0003571",
                        "UPHENO:0014351",
                        "UPHENO:0088162",
                        "UPHENO:0002987",
                        "UPHENO:0076702",
                        "UPHENO:0005230",
                        "UPHENO:0056250",
                        "UPHENO:0014320",
                        "UPHENO:0063577",
                        "UPHENO:0085410",
                        "UPHENO:0056237",
                        "UBERON:0005629",
                        "UBERON:0006876",
                        "UBERON:0036302",
                        "UPHENO:0005285",
                        "UBERON:0003914",
                        "HP:0012639",
                        "UPHENO:0002704",
                        "UPHENO:0049873",
                        "UPHENO:0011538",
                        "UPHENO:0002576",
                        "UPHENO:0056150",
                        "UBERON:0000178",
                        "UPHENO:0085938",
                        "UBERON:0004535",
                        "UBERON:0001893",
                        "UPHENO:0004788",
                        "UPHENO:0004507",
                        "UPHENO:0004484",
                        "UBERON:0001049",
                        "UBERON:0000179",
                        "UBERON:0003080",
                        "UPHENO:0056242",
                        "UPHENO:0014291",
                        "UPHENO:0014761",
                        "UBERON:0001009",
                        "UBERON:0007798",
                        "UBERON:0000477",
                        "UPHENO:0003391",
                        "UPHENO:0002839",
                        "UPHENO:0003004",
                        "UPHENO:0088047",
                        "UPHENO:0002736",
                        "GO:0009059",
                        "UPHENO:0056251",
                        "HP:0002977",
                        "UPHENO:0081598",
                        "UPHENO:9002003",
                        "UPHENO:0087518",
                        "UPHENO:0014285",
                        "UPHENO:0004956",
                        "UBERON:0000490",
                        "NCBITaxon:33208",
                        "UBERON:0001048",
                        "UPHENO:0005141",
                        "UBERON:0004128",
                        "UBERON:0003089",
                        "UBERON:0002346",
                        "UBERON:0001032",
                        "UBERON:0007503",
                        "UPHENO:0005097",
                        "UBERON:0000481",
                        "UPHENO:0003191",
                        "UBERON:0002049",
                        "NCBITaxon:131567",
                        "UPHENO:0002866",
                        "UPHENO:0004757",
                        "UPHENO:0056158",
                        "HP:0008056",
                        "UPHENO:0003186",
                        "UBERON:0000060",
                        "UPHENO:0076718",
                        "UBERON:0011143",
                        "UBERON:0003076",
                        "UPHENO:0005214",
                        "HP:0012145",
                        "UPHENO:0087347",
                        "UPHENO:0080079",
                        "GO:0009892",
                        "HP:0011017",
                        "UBERON:0012140",
                        "UBERON:0000479",
                        "UBERON:0034923",
                        "HP:0001871",
                        "UBERON:0004086",
                        "UPHENO:0002668",
                        "UPHENO:0063581",
                        "HP:0012443",
                        "UPHENO:0084763",
                        "UPHENO:0053633",
                        "UPHENO:0011845",
                        "CL:0001035",
                        "UPHENO:0084448",
                        "HP:0005528",
                        "UPHENO:0005284",
                        "UPHENO:0002861",
                        "UBERON:0003460",
                        "UBERON:0004120",
                        "UPHENO:0063558",
                        "UPHENO:0086956",
                        "UBERON:0000383",
                        "UBERON:0002390",
                        "UBERON:0002616",
                        "UPHENO:0047287",
                        "UPHENO:0002554",
                        "UPHENO:0047419",
                        "HP:0010935",
                        "UPHENO:0081451",
                        "UPHENO:0003092",
                        "UPHENO:0087501",
                        "UBERON:0001555",
                        "UBERON:0001008",
                        "UPHENO:0002642",
                        "UPHENO:0047344",
                        "UPHENO:0087472",
                        "UPHENO:0053580",
                        "UPHENO:0003093",
                        "GO:0040007",
                        "UPHENO:0080209",
                        "UBERON:0003913",
                        "HP:0000001",
                        "UPHENO:0004885",
                        "UPHENO:0053566",
                        "UPHENO:0003936",
                        "UBERON:0003103",
                        "UPHENO:0002648",
                        "UBERON:0002386",
                        "UBERON:0004375",
                        "UPHENO:0002731",
                        "UPHENO:0053561",
                        "HP:0007364",
                        "UBERON:0004381",
                        "HP:0000077",
                        "UBERON:0000033",
                        "UPHENO:0002635",
                        "UPHENO:0004143",
                        "UBERON:0000926",
                        "HP:0000086",
                        "UPHENO:0076957",
                        "UPHENO:0003049",
                        "UPHENO:0074245",
                        "UPHENO:0002909",
                        "UPHENO:0002944",
                        "GO:0031052",
                        "UBERON:0002193",
                        "UPHENO:0026183",
                        "UBERON:8450002",
                        "UBERON:0000026",
                        "HP:0040064",
                        "UPHENO:0053643",
                        "UPHENO:3000004",
                        "UBERON:0002417",
                        "UPHENO:0075220",
                        "BFO:0000015",
                        "GO:0003008",
                        "UPHENO:0002593",
                        "UPHENO:0047355",
                        "UPHENO:0071308",
                        "BFO:0000003",
                        "UBERON:0001016",
                        "UPHENO:0001001",
                        "UPHENO:0063594",
                        "HP:0003330",
                        "HP:0009804",
                        "HP:0000125",
                        "UBERON:0005173",
                        "UPHENO:0087349",
                        "UBERON:0009569",
                        "UPHENO:0002733",
                        "HP:0000707",
                        "UBERON:0003466",
                        "GO:0050890",
                        "UPHENO:0076800",
                        "HP:0011446",
                        "GO:0065007",
                        "UBERON:0008785",
                        "GO:0009889",
                        "UBERON:0005282",
                        "HP:0002818",
                        "UPHENO:0087427",
                        "UPHENO:0047285",
                        "HP:0000924",
                        "UPHENO:0002433",
                        "UBERON:0001474",
                        "UPHENO:0000543",
                        "GO:0050789",
                        "UPHENO:0002949",
                        "UPHENO:0080114",
                        "UPHENO:0002905",
                        "UBERON:0000165",
                        "UPHENO:0002859",
                        "UPHENO:0003025",
                        "UBERON:0004122",
                        "UPHENO:0063849",
                        "CL:0002092",
                        "UPHENO:0002945",
                        "UPHENO:0002525",
                        "UPHENO:0087665",
                        "UPHENO:0008548",
                        "HP:0011282",
                        "UPHENO:0002967",
                        "UBERON:0000466",
                        "UPHENO:0086679",
                        "UPHENO:0002531",
                        "HP:0001167",
                        "UPHENO:0004621",
                        "UPHENO:0002536",
                        "UBERON:0000075",
                        "UBERON:0005358",
                        "UBERON:0013522",
                        "UPHENO:0011536",
                        "UPHENO:0069062",
                        "UPHENO:0049835",
                        "UBERON:0001091",
                        "UPHENO:0026078",
                        "UPHENO:0014971",
                        "UPHENO:0049874",
                        "UPHENO:0080325",
                        "UPHENO:0002558",
                        "UBERON:0003071",
                        "UPHENO:0047376",
                        "UPHENO:0056226",
                        "UPHENO:3000000",
                        "UPHENO:0002267",
                        "UPHENO:0049587",
                        "HP:0000163",
                        "UPHENO:3000007",
                        "UPHENO:0003088",
                        "UPHENO:0087663",
                        "UPHENO:0053588",
                        "GO:0009987",
                        "HP:0005561",
                        "UBERON:0005291",
                        "UBERON:0010312",
                        "UPHENO:0002844",
                        "GO:0010467",
                        "UPHENO:0002826",
                        "UPHENO:0049904",
                        "UPHENO:0002764",
                        "UBERON:0000061",
                        "UPHENO:0011531",
                        "UPHENO:0035151",
                        "UPHENO:0076803",
                        "UPHENO:0002269",
                        "UPHENO:0053619",
                        "UPHENO:0003189",
                        "GO:0050877",
                        "UBERON:0013702",
                        "UBERON:0005281",
                        "UPHENO:0004680",
                        "UPHENO:0076703",
                        "UPHENO:0014292",
                        "UPHENO:0002988",
                        "HP:0009777",
                        "GO:0008150",
                        "UBERON:0006601",
                        "HP:0040068",
                        "UPHENO:0004505",
                        "HP:0000234",
                        "GO:0010605",
                        "UBERON:0015061",
                        "UPHENO:0063731",
                        "UBERON:0000475",
                        "UBERON:0000468",
                        "UBERON:0016880",
                        "UPHENO:0053632",
                        "UPHENO:0076786",
                        "UPHENO:0002928",
                        "UPHENO:0002527",
                        "CL:0000255",
                        "HP:0002143",
                        "UBERON:0001062",
                        "UBERON:0000153",
                        "UPHENO:0011586",
                        "UBERON:0034925",
                        "UBERON:0000467",
                        "UPHENO:0005092",
                        "UPHENO:0002385",
                        "HP:0031816",
                        "UPHENO:0011589",
                        "UPHENO:0004459",
                        "UBERON:0001460",
                        "UPHENO:0011568",
                        "UPHENO:0002833",
                        "GO:0009058",
                        "UBERON:0003102",
                        "UPHENO:0002637",
                        "UBERON:0002371",
                        "UBERON:0012141",
                        "UPHENO:0088123",
                        "UBERON:0005423",
                        "UPHENO:0004615",
                        "HP:0000079",
                        "UPHENO:0002870",
                        "UPHENO:0025509",
                        "UPHENO:0004519",
                        "UBERON:0002050",
                        "UBERON:0000483",
                        "UPHENO:0002976",
                        "UPHENO:0002530",
                        "UPHENO:0003334",
                        "UPHENO:0003069",
                        "UPHENO:0069266",
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                        "UBERON:0010708",
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                        "UPHENO:0075902",
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                        "UPHENO:0056333",
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                        "UBERON:0004088",
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                        "UPHENO:0002785",
                        "UPHENO:0004494",
                        "UPHENO:0047299",
                        "UPHENO:0011509",
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                        "HP:0033127",
                        "UBERON:0010316",
                        "UPHENO:0075219",
                        "UBERON:0002102",
                        "UPHENO:0002767",
                        "UPHENO:0047411",
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                        "UPHENO:0035160",
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                        "UBERON:0004357",
                        "UBERON:0010000",
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                        "HP:0002817",
                        "HP:0031938",
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                        "UPHENO:0047425",
                        "UBERON:0013701",
                        "UBERON:0008962",
                        "UPHENO:0026108",
                        "GO:0010558",
                        "UBERON:0015001",
                        "UPHENO:0002816",
                        "UBERON:0001017",
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                        "HP:0010674",
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                        "UPHENO:0008668",
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                        "HP:0040070",
                        "UPHENO:0068914",
                        "HP:0001155",
                        "UPHENO:0004888",
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                        "UBERON:0001423",
                        "CL:0000329",
                        "UPHENO:0082875",
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                        "UBERON:0010538",
                        "UBERON:0001463",
                        "UBERON:0010363",
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                        "HP:0002813",
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                        "UBERON:0000063",
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                        "HP:0000929",
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                        "UPHENO:0047409",
                        "HP:0000478",
                        "UPHENO:0086635",
                        "UPHENO:0002571",
                        "UPHENO:0003005",
                        "RO:0002577",
                        "UBERON:0002389",
                        "BFO:0000004",
                        "UBERON:0000019",
                        "UPHENO:0002567",
                        "UPHENO:0076779",
                        "UPHENO:0004482",
                        "UBERON:0000167",
                        "UPHENO:0002891",
                        "UPHENO:0087849",
                        "UBERON:0009142",
                        "UPHENO:0005110",
                        "UBERON:0000073",
                        "UPHENO:0002594",
                        "GO:0009890",
                        "UBERON:0011216",
                        "UBERON:0004347",
                        "UPHENO:0002719",
                        "UBERON:0005417",
                        "UPHENO:0002526",
                        "UPHENO:0002964",
                        "UBERON:0004456",
                        "UPHENO:0026181",
                        "UPHENO:0026146",
                        "UBERON:0012354",
                        "HP:0012638",
                        "UPHENO:0086700",
                        "UPHENO:0002803",
                        "UPHENO:0002782",
                        "UPHENO:0080099",
                        "UPHENO:0002678",
                        "UPHENO:0009382",
                        "UPHENO:0009163",
                        "UPHENO:0027017",
                        "GO:0050794",
                        "UPHENO:0009209",
                        "UPHENO:0081466",
                        "UBERON:0000307",
                        "UPHENO:0004909",
                        "UPHENO:0005030",
                        "UBERON:5002389",
                        "UPHENO:0088185",
                        "UPHENO:0086486",
                        "HP:0009601",
                        "UPHENO:0002765",
                        "UPHENO:0084761",
                        "UBERON:0002513",
                        "HP:0011297",
                        "UPHENO:0009020",
                        "UBERON:0010130",
                        "UBERON:0001015",
                        "HP:0009815",
                        "UBERON:5001463",
                        "UPHENO:0087661",
                        "UBERON:0019221",
                        "UBERON:0006717",
                        "UPHENO:0011825",
                        "UPHENO:0026640",
                        "UPHENO:0002577",
                        "HP:0006496",
                        "UBERON:0000047",
                        "HP:0009115",
                        "UBERON:0005451",
                        "UBERON:0004708",
                        "UBERON:0002398",
                        "UBERON:0002091",
                        "UPHENO:0004476",
                        "CL:0000763",
                        "UPHENO:0086485",
                        "UPHENO:0076739",
                        "UPHENO:0050121",
                        "UPHENO:0088170",
                        "UPHENO:0076692",
                        "HP:0009380",
                        "UPHENO:0025587",
                        "HP:0040072",
                        "UBERON:5006048",
                        "GO:0042592",
                        "UPHENO:0001003",
                        "UBERON:0002470",
                        "UPHENO:0075997",
                        "UPHENO:0002659",
                        "HP:0045060",
                        "UPHENO:0004433",
                        "UBERON:0001442",
                        "UPHENO:0002559",
                        "UPHENO:0002902",
                        "HP:0002973",
                        "UBERON:0003607",
                        "UPHENO:0076723",
                        "UPHENO:0026506",
                        "HP:0001172",
                        "HP:0003764",
                        "UPHENO:0003181",
                        "UPHENO:0053601",
                        "HP:0006265",
                        "UBERON:5002544",
                        "GO:0048523",
                        "UPHENO:0025507",
                        "UPHENO:0086589",
                        "HP:0000568",
                        "UPHENO:0005055",
                        "UPHENO:0018390",
                        "UPHENO:0002553",
                        "NCBITaxon:33154",
                        "UPHENO:0002926",
                        "UPHENO:0004892",
                        "UBERON:0010230",
                        "UBERON:0010740",
                        "UPHENO:0068971",
                        "UBERON:0012139",
                        "UBERON:0003056",
                        "NCBITaxon:2759",
                        "UBERON:0016879",
                        "UPHENO:0047289",
                        "NCBITaxon:1",
                        "UBERON:0001890",
                        "HP:0011044",
                        "UBERON:0003072",
                        "HP:0100547",
                        "CL:0000988",
                        "UPHENO:0075195",
                        "UPHENO:0005058",
                        "UBERON:0002553",
                        "NCBITaxon:6072",
                        "UPHENO:0069523",
                        "GO:0019222",
                        "UPHENO:0002963",
                        "UPHENO:0087924",
                    ],
                    "has_phenotype_closure_label": [
                        "Abnormal skull morphology",
                        "Aplasia/Hypoplasia involving the central nervous system",
                        "Microcephaly",
                        "Abnormal forebrain morphology",
                        "skull phenotype",
                        "forebrain morphology phenotype",
                        "Abnormal cerebral morphology",
                        "integument phenotype",
                        "Nevus",
                        "integumental system phenotype",
                        "skin of body",
                        "Abnormal skin morphology",
                        "skin of body morphology phenotype",
                        "Abnormal digestive system morphology",
                        "closing of the anatomical conduit",
                        "ectoderm-derived structure atresia",
                        "closing of the ectoderm-derived structure",
                        "anus morphology phenotype",
                        "Abnormality of the anus",
                        "orifice",
                        "orifice atresia",
                        "Anal atresia",
                        "anus atresia",
                        "closing of the anatomical structure",
                        "closing of the multicellular anatomical structure",
                        "developing mesenchymal condensation",
                        "axial skeleton plus cranial skeleton",
                        "closing of the material anatomical entity",
                        "postcranial axial skeleton",
                        "postcranial axial skeletal system",
                        "presumptive paraxial mesoderm phenotype",
                        "presomitic mesoderm phenotype",
                        "somite phenotype",
                        "migrating mesenchyme population phenotype",
                        "presumptive paraxial mesoderm",
                        "Abnormal curvature of the vertebral column",
                        "epithelial vesicle",
                        "multicellular anatomical structure atresia",
                        "cell condensation",
                        "paraxial mesoderm",
                        "vertebral column phenotype",
                        "presomitic mesoderm",
                        "skull",
                        "cell condensation phenotype",
                        "Abnormality of the integument",
                        "dorsal region element phenotype",
                        "spinal cord",
                        "Tethered cord",
                        "Abnormal conus terminalis morphology",
                        "Abnormal spinal cord morphology",
                        "spinal cord morphology phenotype",
                        "dorsal region element",
                        "Neurodevelopmental delay",
                        "Motor delay",
                        "Delayed gross motor development",
                        "programmed DNA elimination by chromosome breakage",
                        "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",
                        "gene expression phenotype",
                        "regulation of cellular process",
                        "biosynthetic process",
                        "macromolecule metabolic process",
                        "anatomical entity atresia",
                        "Chromosome breakage",
                        "homeostatic process",
                        "biological regulation",
                        "biosynthetic process phenotype",
                        "Abnormality of chromosome stability",
                        "regulation of macromolecule biosynthetic process",
                        "negative regulation of macromolecule metabolic process",
                        "Abnormality of metabolism/homeostasis",
                        "regulation of macromolecule metabolic process",
                        "trunk mesenchyme",
                        "regulation of biosynthetic process",
                        "negative regulation of metabolic process",
                        "blood cell phenotype",
                        "myeloid cell",
                        "Abnormal erythrocyte morphology",
                        "cell phenotype",
                        "oxygen accumulating cell",
                        "Chiari type I malformation",
                        "segmental subdivision of hindbrain phenotype",
                        "hindbrain phenotype",
                        "segmental subdivision of hindbrain",
                        "posterior neural tube phenotype",
                        "organ subunit",
                        "formed cerebellum",
                        "skin of body phenotype",
                        "Cerebellar malformation",
                        "formed regional part of nervous system",
                        "hindbrain morphology phenotype",
                        "formed multicellular anatomical structure",
                        "Abnormal metencephalon morphology",
                        "metencephalon morphology phenotype",
                        "metencephalon",
                        "Abnormal cerebellum morphology",
                        "chordal neural plate phenotype",
                        "anatomical entity morphology in the brain phenotype",
                        "Abnormal hindbrain morphology",
                        "chordal neural plate",
                        "bodily fluid",
                        "increased number of organ part in the cerebrospinal fluid",
                        "increased number of organ component layer",
                        "vascular system",
                        "segmental subdivision of nervous system phenotype",
                        "increased number of brain ventricle in the cerebrospinal fluid",
                        "Abnormal cerebrospinal fluid morphology",
                        "number of anatomical entities of type anatomical entity in blood phenotype",
                        "increased number of ectoderm-derived structure in the cerebrospinal fluid",
                        "vasculature",
                        "increased number of anatomical entity",
                        "Aplasia/Hypoplasia of the cerebrum",
                        "increased number of material anatomical entity in the cerebrospinal fluid",
                        "central nervous system",
                        "brain ventricle morphology phenotype",
                        "increased number of ectoderm-derived structure",
                        "increased number of anatomical structure",
                        "increased number of brain ventricle/choroid plexus",
                        "cerebrospinal fluid morphology phenotype",
                        "brain ventricle/choroid plexus phenotype",
                        "number of anatomical enitites of type organ part phenotype",
                        "vasculature phenotype",
                        "anatomical wall",
                        "organ component layer",
                        "regional part of nervous system",
                        "increased number of anatomical entity in the blood",
                        "ventricle of nervous system",
                        "regional part of brain",
                        "anatomical conduit atresia",
                        "Scoliosis",
                        "cerebrospinal fluid",
                        "blood island",
                        "organ component layer phenotype",
                        "nervous system morphology phenotype",
                        "vascular plexus phenotype",
                        "Abnormal cellular physiology",
                        "increased number of anatomical entity in the cerebrospinal fluid",
                        "increased number of multicellular anatomical structure in the cerebrospinal fluid",
                        "central nervous system morphology phenotype",
                        "brain",
                        "Anemia",
                        "telencephalon",
                        "sclerotome phenotype",
                        "formed material anatomical entity",
                        "brain phenotype",
                        "epithelial tube",
                        "regulation of gene expression",
                        "regional part of brain phenotype",
                        "brain ventricle/choroid plexus morphology phenotype",
                        "increased number of organ part",
                        "vascular plexus",
                        "vasculature of central nervous system plus retina",
                        "epithelial tube phenotype",
                        "increased number of ventricle of nervous system in the cerebrospinal fluid",
                        "cerebrospinal fluid phenotype",
                        "increased number of anatomical structure in the cerebrospinal fluid",
                        "brain ventricle phenotype",
                        "neural tube phenotype",
                        "anatomical cluster",
                        "Abnormal nervous system morphology",
                        "Abnormal cerebral ventricle morphology",
                        "paraxial mesoderm phenotype",
                        "erythrocyte morphology phenotype",
                        "haemolymphatic fluid",
                        "transudate",
                        "anterior neural tube",
                        "organism substance",
                        "anatomical wall phenotype",
                        "increased number of ventricle of nervous system",
                        "telencephalon phenotype",
                        "pre-chordal neural plate",
                        "Eumetazoa",
                        "immature eye",
                        "root",
                        "haemolymphatic fluid phenotype",
                        "gastrula morphology phenotype",
                        "size of eyeball of camera-type eye phenotype",
                        "gastrula",
                        "eye",
                        "epithelium",
                        "entire sense organ system",
                        "multi-tissue structure phenotype",
                        "Microphthalmia",
                        "craniocervical region morphology phenotype",
                        "anus",
                        "unilaminar epithelium phenotype",
                        "ectoderm",
                        "neural plate",
                        "negative regulation of gene expression",
                        "future central nervous system phenotype",
                        "optic cup",
                        "paired limb/fin segment",
                        "anatomical structure physiology phenotype",
                        "blood island phenotype",
                        "decreased number of anatomical entity",
                        "digit 1 phenotype",
                        "anatomical space",
                        "paired limb/fin segment phenotype",
                        "mesoderm-derived structure phenotype",
                        "negative regulation of gene expression phenotype",
                        "vasculature of organ",
                        "trunk region element phenotype",
                        "bone of appendage girdle complex",
                        "absent multicellular anatomical structure in the limb",
                        "Abnormal bone marrow cell morphology",
                        "forebrain phenotype",
                        "nervous system physiology phenotype",
                        "obsolete cell",
                        "digestive system",
                        "paired limb/fin bud phenotype",
                        "eukaryotic cell",
                        "upper limb segment phenotype",
                        "skeleton",
                        "skeletal element phenotype",
                        "presumptive structure phenotype",
                        "disconnected anatomical group",
                        "Abnormality of multiple cell lineages in the bone marrow",
                        "cerebellum morphology phenotype",
                        "bone marrow cell",
                        "lateral structure",
                        "absent anatomical structure",
                        "Abnormality of the genitourinary system",
                        "localised abdominal segment element",
                        "anatomical structure phenotype",
                        "Abnormality of the digestive system",
                        "bone marrow",
                        "ventricular system of central nervous system",
                        "subdivision of tube",
                        "localised anatomical structure",
                        "autopod region phenotype",
                        "subdivision of trunk phenotype",
                        "localised trunk region element",
                        "ventricular system of brain",
                        "compound organ",
                        "kidney phenotype",
                        "Abnormality of the upper urinary tract",
                        "Abnormal brain morphology",
                        "localised lateral structure",
                        "organism substance phenotype",
                        "Abnormality of the urinary system",
                        "localised anatomical entity",
                        "absent anatomical structure in the multicellular organism",
                        "renal system",
                        "lateral structure phenotype",
                        "upper urinary tract",
                        "aplastic secondary dentition",
                        "trunk phenotype",
                        "Ectopic kidney",
                        "trunk region element",
                        "abdominal segment element phenotype",
                        "excretory system",
                        "head morphology phenotype",
                        "sensory system",
                        "Growth abnormality",
                        "limb bud",
                        "size of skull phenotype",
                        "growth phenotype",
                        "appendage girdle complex",
                        "subdivision of skeletal system phenotype",
                        "growth",
                        "cavitated compound organ",
                        "manual digit phenotype",
                        "trunk",
                        "skeleton phenotype",
                        "material anatomical entity physiology phenotype",
                        "Abnormality of the nervous system",
                        "number of anatomical enitites of type organ component layer phenotype",
                        "process",
                        "multicellular anatomical structure",
                        "aplasia or hypoplasia of telencephalon",
                        "manual digit plus metapodial segment",
                        "telencephalon morphology phenotype",
                        "cardiovascular system phenotype",
                        "anatomical system physiology phenotype",
                        "hematopoietic system phenotype",
                        "Morphological central nervous system abnormality",
                        "cognition",
                        "number of anatomical enitites of type ectoderm-derived structure phenotype",
                        "pectoral appendage",
                        "delayed biological_process",
                        "decreased number of structure with developmental contribution from neural crest",
                        "Abnormal nervous system physiology",
                        "nervous system process",
                        "dentition",
                        "organism subdivision phenotype",
                        "dysgenesis of the forelimb zeugopod bone",
                        "appendicular skeleton phenotype",
                        "sense organ phenotype",
                        "location of anatomical entity phenotype",
                        "Abnormality of skull size",
                        "anatomical cavity phenotype",
                        "nervous system phenotype",
                        "decreased number of calcareous tooth",
                        "blastula",
                        "skeletal system phenotype",
                        "decreased number of anatomical structure",
                        "Abnormal number of teeth",
                        "forelimb zeugopod",
                        "Chiari malformation",
                        "aplasia or hypoplasia of manual digit",
                        "Abnormal oral cavity morphology",
                        "arm bone phenotype",
                        "segmental subdivision of nervous system",
                        "oral cavity phenotype",
                        "abdominal segment of trunk",
                        "Abnormal renal morphology",
                        "subdivision of digestive tract",
                        "developing anatomical structure phenotype",
                        "calcareous tooth phenotype",
                        "abdominal segment element",
                        "closing of the anatomical entity",
                        "number of anatomical enitites of type skeletal element phenotype",
                        "material anatomical entity",
                        "circulatory system",
                        "autopod region",
                        "mesoderm phenotype",
                        "epithelial vesicle phenotype",
                        "decreased number of organ",
                        "increased number of brain ventricle/choroid plexus in the cerebrospinal fluid",
                        "forelimb endochondral element phenotype",
                        "spinal cord phenotype",
                        "craniofacial/craniocervical phenotype",
                        "agenesis of anatomical entity",
                        "Finger aplasia",
                        "ecto-epithelium",
                        "dorsum",
                        "vasculature of central nervous system plus retina phenotype",
                        "nervous system",
                        "subdivision of digestive tract phenotype",
                        "body proper",
                        "structure with developmental contribution from neural crest phenotype",
                        "bone element",
                        "subdivision of organism along appendicular axis",
                        "forelimb zeugopod bone",
                        "somite",
                        "decreased size of the multicellular anatomical structure",
                        "mesoderm morphology phenotype",
                        "Abnormal number of permanent teeth",
                        "material anatomical entity phenotype",
                        "absent material anatomical entity in the limb",
                        "number of anatomical enitites of type multicellular anatomical structure phenotype",
                        "segment of autopod",
                        "kidney morphology phenotype",
                        "cerebellum",
                        "dysgenesis of the endochondral element",
                        "metabolic process phenotype",
                        "phenotype",
                        "Tooth agenesis",
                        "aplasia or hypoplasia of anatomical entity",
                        "musculoskeletal system phenotype",
                        "organ system subdivision",
                        "circulatory system phenotype",
                        "absent anatomical structure in the limb",
                        "organ part phenotype",
                        "anatomical system",
                        "Abnormal bone structure",
                        "number of anatomical enitites of type tooth-like structure phenotype",
                        "Growth delay",
                        "bone of free limb or fin phenotype",
                        "paired limb/fin skeleton phenotype",
                        "anatomical entity",
                        "embryonic structure",
                        "limb phenotype",
                        "non-connected functional system",
                        "forelimb long bone",
                        "structure with developmental contribution from neural crest",
                        "tooth-like structure",
                        "Absent thumb",
                        "Delayed ability to walk",
                        "blood",
                        "embryonic structure phenotype",
                        "number of anatomical enitites of type material anatomical entity phenotype",
                        "Hydrocephalus",
                        "secondary dentition",
                        "taxon specific phenotype",
                        "multicellular organism",
                        "vertebral column",
                        "axial skeletal system",
                        "limb endochondral element",
                        "paired limb/fin bud",
                        "phenotypic effect",
                        "immune system",
                        "forelimb bud morphology phenotype",
                        "decreased number of ectoderm-derived structure",
                        "size of anatomical entity phenotype",
                        "organ part",
                        "surface structure",
                        "limb long bone morphology phenotype",
                        "cell",
                        "dysgenesis of the anatomical entity",
                        "trunk mesenchyme phenotype",
                        "head",
                        "Bone marrow hypocellularity",
                        "Localized skin lesion",
                        "embryo",
                        "Pelvic kidney",
                        "optic vesicle phenotype",
                        "anterior region of body",
                        "subdivision of head phenotype",
                        "manual digitopodium region",
                        "decreased number of tooth-like structure",
                        "endochondral element",
                        "Abnormality of the eye",
                        "Abnormality of the kidney",
                        "Abnormality of the upper limb",
                        "orbital region phenotype",
                        "pectoral complex",
                        "blood cell",
                        "Abnormality of the face",
                        "programmed DNA elimination by chromosome breakage phenotype",
                        "anatomical entity physiology phenotype",
                        "subdivision of organism along main body axis phenotype",
                        "number of anatomical enitites of type anatomical collection phenotype",
                        "anatomical entity morphology in the appendage girdle complex phenotype",
                        "pre-chordal neural plate phenotype",
                        "hematopoietic system",
                        "Phenotypic abnormality",
                        "limb skeleton subdivision",
                        "Abnormality of the skin",
                        "anatomical space phenotype",
                        "dysgenesis of the long bone",
                        "dentition phenotype",
                        "number of anatomical enitites of type dentition phenotype",
                        "vasculature of organ phenotype",
                        "neural plate morphology phenotype",
                        "localised organ",
                        "number of anatomical enitites of type organ phenotype",
                        "Abnormality of mental function",
                        "epithelium phenotype",
                        "neural tube morphology phenotype",
                        "bone of pectoral complex morphology phenotype",
                        "decreased size of the anatomical entity",
                        "skeletal system morphology phenotype",
                        "manus morphology phenotype",
                        "Abnormality of the musculoskeletal system",
                        "dysgenesis of the bone of appendage girdle complex",
                        "Agenesis of permanent teeth",
                        "paired limb/fin phenotype",
                        "musculoskeletal system",
                        "decreased number of skeletal element",
                        "Abnormal localization of kidney",
                        "Radial dysplasia",
                        "metabolic process",
                        "primordium phenotype",
                        "cerebellum phenotype",
                        "tooth-like structure phenotype",
                        "increased number of material anatomical entity",
                        "face",
                        "regional part of nervous system phenotype",
                        "face phenotype",
                        "vision/eye phenotype",
                        "aplasia or hypoplasia of eyeball of camera-type eye",
                        "abdomen",
                        "brain ventricle/choroid plexus",
                        "dysgenesis of the limb long bone",
                        "surface structure phenotype",
                        "anatomical entity morphology in the manus phenotype",
                        "independent continuant",
                        "system process",
                        "number of anatomical enitites of type anatomical structure phenotype",
                        "hemolymphoid system",
                        "main body axis",
                        "upper urinary tract phenotype",
                        "localised kidney",
                        "craniocervical region",
                        "blood phenotype",
                        "bone cell",
                        "manual digit 1",
                        "formed ectoderm-derived structure",
                        "number of anatomical enitites of type anatomical entity phenotype",
                        "All",
                        "subdivision of head",
                        "calcareous tooth",
                        "dysgenesis of the bone element",
                        "anatomical cavity",
                        "number of anatomical enitites of type calcareous tooth phenotype",
                        "decreased number of multicellular anatomical structure",
                        "multi-limb segment region",
                        "decreased number of anatomical entity in the multicellular organism",
                        "skeletal element",
                        "compound organ phenotype",
                        "craniocervical region phenotype",
                        "central nervous system phenotype",
                        "pectoral appendage bud",
                        "formed multi-tissue structure",
                        "sensory system phenotype",
                        "anatomical conduit phenotype",
                        "Abnormality of limbs",
                        "macromolecule metabolic process phenotype",
                        "organ",
                        "organism subdivision",
                        "absent multicellular anatomical structure",
                        "anatomical conduit",
                        "hindbrain",
                        "multicellular organismal process",
                        "dysgenesis of the mesoderm-derived structure",
                        "digit plus metapodial segment",
                        "material anatomical entity atresia",
                        "camera-type eye phenotype",
                        "material entity",
                        "Abnormality of globe size",
                        "anatomical entity phenotype",
                        "genitourinary system phenotype",
                        "presumptive structure",
                        "number of anatomical enitites of type secondary dentition phenotype",
                        "regulation of biological process",
                        "Abnormality of the skeletal system",
                        "optic cup morphology phenotype",
                        "embryo phenotype",
                        "decreased number of multicellular anatomical structure in the multicellular organism",
                        "subdivision of skeletal system",
                        "mouth",
                        "dysgenesis of the endochondral bone",
                        "embryonic tissue",
                        "negative regulation of biological process",
                        "Abnormal oral morphology",
                        "number of anatomical enitites of type structure with developmental contribution from neural crest phenotype",
                        "limb bone morphology phenotype",
                        "Abnormality of the mouth",
                        "dysgenesis of the arm bone",
                        "renal/urinary system phenotype",
                        "biological_process phenotype",
                        "oral cavity",
                        "localised compound organ",
                        "sense organ",
                        "erythrocyte",
                        "increased number of organ component layer in the cerebrospinal fluid",
                        "tube phenotype",
                        "orifice phenotype",
                        "digestive system morphology phenotype",
                        "negative regulation of cellular process",
                        "Abnormality of the head",
                        "digestive system phenotype",
                        "localised multicellular anatomical structure",
                        "multicellular organism morphology phenotype",
                        "continuant",
                        "anus phenotype",
                        "entity",
                        "immaterial anatomical entity phenotype",
                        "kidney",
                        "zeugopodial skeleton",
                        "dysgenesis of the forelimb bone",
                        "anatomical entity morphology phenotype",
                        "anatomical system phenotype",
                        "zeugopod",
                        "negative regulation of biosynthetic process",
                        "decreased size of the sense organ",
                        "malformed anatomical entity",
                        "cavitated compound organ phenotype",
                        "anatomical structure",
                        "mouth phenotype",
                        "skeletal system",
                        "head phenotype",
                        "localised cavitated compound organ",
                        "immaterial entity",
                        "localised abdomen element",
                        "occurrent",
                        "limb morphology phenotype",
                        "ectoderm phenotype",
                        "subdivision of trunk",
                        "Intellectual disability",
                        "segment of manus",
                        "pectoral appendage skeleton",
                        "aplastic anatomical entity",
                        "paired limb/fin",
                        "brain ventricle",
                        "limb skeleton subdivision phenotype",
                        "increased number of multicellular anatomical structure",
                        "endochondral bone phenotype",
                        "digit morphology phenotype",
                        "radius bone phenotype",
                        "dysgenesis of the skeletal element",
                        "forelimb skeleton phenotype",
                        "ectoderm-derived structure",
                        "dysgenesis of the radius endochondral element",
                        "integumental system",
                        "organ subunit phenotype",
                        "anatomical cluster phenotype",
                        "ectoderm-derived structure phenotype",
                        "anatomical entity morphology in the skeleton of pectoral complex phenotype",
                        "forelimb bud",
                        "Abnormal anus morphology",
                        "appendage phenotype",
                        "germ layer phenotype",
                        "abdomen element phenotype",
                        "limb segment phenotype",
                        "endochondral element phenotype",
                        "forelimb zeugopod phenotype",
                        "mouth morphology phenotype",
                        "limb endochondral element phenotype",
                        "bone of pectoral complex phenotype",
                        "Abnormal upper limb bone morphology",
                        "bodily fluid phenotype",
                        "endochondral bone",
                        "long bone",
                        "limb segment",
                        "Abnormality of limb bone",
                        "dysgenesis of the organ",
                        "arm",
                        "decreased size of the eyeball of camera-type eye",
                        "Decreased head circumference",
                        "tissue phenotype",
                        "pectoral appendage bud phenotype",
                        "long bone phenotype",
                        "anatomical collection phenotype",
                        "dysgenesis of the forelimb long bone",
                        "anatomical entity morphology in the pectoral complex phenotype",
                        "appendage",
                        "neurectoderm phenotype",
                        "germ layer / neural crest phenotype",
                        "forelimb morphology phenotype",
                        "mesenchyme morphology phenotype",
                        "lateral plate mesoderm phenotype",
                        "primordium",
                        "localised material anatomical entity",
                        "dysgenesis of the limb bone",
                        "forelimb bone phenotype",
                        "Abnormal appendicular skeleton morphology",
                        "lateral plate mesoderm",
                        "absent autopodial extension",
                        "germ layer",
                        "limb",
                        "erythroid lineage cell",
                        "radius bone morphology phenotype",
                        "metencephalon phenotype",
                        "mesoderm-derived structure",
                        "forelimb skeleton",
                        "zeugopod phenotype",
                        "musculature of body phenotype",
                        "delayed growth",
                        "digit 1",
                        "arm phenotype",
                        "bone of pectoral complex",
                        "bone of free limb or fin",
                        "anatomical structure atresia",
                        "formed regional part of brain",
                        "Abnormality of head or neck",
                        "limb bone",
                        "long bone morphology phenotype",
                        "limb long bone",
                        "embryo morphology phenotype",
                        "Opisthokonta",
                        "forelimb endochondral element",
                        "dysgenesis of the material anatomical entity",
                        "forelimb zeugopod skeleton",
                        "bone of appendage girdle complex phenotype",
                        "embryonic tissue phenotype",
                        "subdivision of organism along main body axis",
                        "germ layer morphology phenotype",
                        "subdivision of skeleton phenotype",
                        "dysgenesis of the forelimb endochondral element",
                        "genitourinary system",
                        "limb long bone phenotype",
                        "skeleton of limb phenotype",
                        "forelimb bud phenotype",
                        "simple eye",
                        "germ layer / neural crest",
                        "dysgenesis of the radius bone",
                        "absent material anatomical entity in the forelimb",
                        "Abnormal forearm morphology",
                        "Neurodevelopmental abnormality",
                        "system",
                        "limb bone phenotype",
                        "biological_process",
                        "multi-limb segment region phenotype",
                        "forelimb bone",
                        "radius endochondral element",
                        "musculature phenotype",
                        "dysgenesis of the bone of pectoral complex",
                        "increased number of brain ventricle",
                        "ecto-epithelium phenotype",
                        "face morphology phenotype",
                        "autopodial extension",
                        "dysgenesis of the multicellular anatomical structure",
                        "multicellular organism phenotype",
                        "simple eye phenotype",
                        "subdivision of tube phenotype",
                        "musculature",
                        "Abnormal axial skeleton morphology",
                        "subdivision of skeleton",
                        "skeleton of pectoral complex",
                        "cranial skeletal system",
                        "appendicular skeleton",
                        "radius bone",
                        "arm bone",
                        "developing anatomical structure",
                        "dysgenesis of the bone of free limb or fin",
                        "gene expression",
                        "Abnormal morphology of the radius",
                        "forelimb phenotype",
                        "absent digit",
                        "sclerotome",
                        "paired limb/fin skeleton",
                        "Aplasia/Hypoplasia of fingers",
                        "macromolecule biosynthetic process",
                        "mesoderm",
                        "decreased number of material anatomical entity in the multicellular organism",
                        "oral cavity morphology phenotype",
                        "Abnormal forearm bone morphology",
                        "forelimb",
                        "cellular organisms",
                        "appendicular skeleton morphology phenotype",
                        "entire embryonic mesenchyme",
                        "abdomen element",
                        "dysgenesis of the limb endochondral element",
                        "renal system morphology phenotype",
                        "forelimb long bone phenotype",
                        "Abnormality of the dentition",
                        "manus phenotype",
                        "mesenchyme phenotype",
                        "dense mesenchyme tissue phenotype",
                        "presumptive ectoderm",
                        "forelimb zeugopod bone phenotype",
                        "limb bud phenotype",
                        "digestive tract",
                        "mesenchyme",
                        "Abnormal skeletal morphology",
                        "absent material anatomical entity in the limb bud",
                        "embryonic tissue morphology phenotype",
                        "integument",
                        "forelimb zeugopod bone morphology phenotype",
                        "appendicular skeletal system",
                        "anterior neural tube phenotype",
                        "dysgenesis of the anatomical structure",
                        "formed anatomical structure",
                        "limb bud morphology phenotype",
                        "organ system subdivision phenotype",
                        "lateral plate mesoderm morphology phenotype",
                        "autopod region morphology phenotype",
                        "Abnormality of the vertebral column",
                        "decreased size of the organ",
                        "skeleton of limb",
                        "dense mesenchyme tissue",
                        "aplasia or hypoplasia of skeleton",
                        "unilaminar epithelium",
                        "digit 1 or 5 phenotype",
                        "digit 1 plus metapodial segment",
                        "autopodial extension phenotype",
                        "pectoral appendage phenotype",
                        "Abnormal finger morphology",
                        "bone element phenotype",
                        "digit phenotype",
                        "posterior neural tube",
                        "Abnormality of blood and blood-forming tissues",
                        "Aplasia/Hypoplasia of the thumb",
                        "absent anatomical structure in the forelimb",
                        "absent multicellular anatomical structure in the multicellular organism",
                        "absent anatomical entity in the multicellular organism",
                        "absent anatomical entity in the limb bud",
                        "upper limb segment",
                        "manual digit 1 plus metapodial segment",
                        "optic vesicle",
                        "absent material anatomical entity in the multicellular organism",
                        "digit 1 or 5",
                        "macromolecule biosynthetic process phenotype",
                        "autopodial skeleton",
                        "Abnormal eye morphology",
                        "absent anatomical entity",
                        "Aplasia/hypoplasia involving bones of the upper limbs",
                        "Aplasia/hypoplasia involving the skeleton",
                        "eyeball of camera-type eye",
                        "forelimb zeugopod morphology phenotype",
                        "Abnormal thumb morphology",
                        "eye primordium phenotype",
                        "absent multicellular anatomical structure in the forelimb",
                        "manual digit morphology in the manus phenotype",
                        "Abnormal digit morphology",
                        "embryonic autopod plate",
                        "Abnormal hand morphology",
                        "migrating mesenchyme population",
                        "organ phenotype",
                        "subdivision of organism along appendicular axis phenotype",
                        "manual digit 1 or 5",
                        "decreased size of the anatomical structure",
                        "absent anatomical entity in the limb",
                        "manual digit",
                        "skeleton of manus",
                        "erythroid lineage cell morphology phenotype",
                        "absent organism subdivision",
                        "forebrain",
                        "decreased number of anatomical structure in the multicellular organism",
                        "absent anatomical entity in the forelimb",
                        "tissue",
                        "absent material anatomical entity",
                        "tube",
                        "cranial skeletal system phenotype",
                        "digitopodium region",
                        "neural tube",
                        "acropodium region",
                        "regulation of metabolic process",
                        "aplasia or hypoplasia of manual digit 1",
                        "manual digit 1 morphology phenotype",
                        "absent organism subdivision in the multicellular organism",
                        "Aplasia/hypoplasia involving bones of the extremities",
                        "decreased size of the material anatomical entity",
                        "Aplasia/hypoplasia involving bones of the hand",
                        "musculature of body",
                        "number of anatomical enitites of type organism subdivision phenotype",
                        "pectoral appendage skeleton phenotype",
                        "Aplasia/hypoplasia of the extremities",
                        "Abnormality of the hand",
                        "embryonic autopod plate morphology phenotype",
                        "aplastic manual digit 1",
                        "Abnormal limb bone morphology",
                        "neurectoderm",
                        "digit",
                        "eyeball of camera-type eye phenotype",
                        "eye primordium",
                        "camera-type eye",
                        "skull morphology phenotype",
                        "programmed DNA elimination",
                        "hematopoietic cell",
                        "orbital region",
                        "cardiovascular system",
                        "eye phenotype",
                        "multi-tissue structure",
                        "brain morphology phenotype",
                        "visual system",
                        "camera-type eye morphology phenotype",
                        "ventricle of nervous system phenotype",
                        "future nervous system",
                        "Eukaryota",
                        "presumptive ectoderm phenotype",
                        "future central nervous system",
                        "immature eye phenotype",
                        "developing mesenchymal condensation phenotype",
                        "anatomical collection",
                        "decreased size of the ectoderm-derived structure",
                        "renal system phenotype",
                        "manus",
                        "ectoderm morphology phenotype",
                        "multicellular anatomical structure phenotype",
                        "Aplasia/Hypoplasia affecting the eye",
                        "absent manual digit",
                        "Metazoa",
                        "decreased number of material anatomical entity",
                        "visual system phenotype",
                        "immaterial anatomical entity",
                        "neural plate phenotype",
                    ],
                    "highlighting": None,
                },
            ],
        },
        "facet_counts": {"facet_fields": {}, "facet_queries": {}},
        "highlighting": {},
    }
