{
  "id": 20260,
  "label": "brachydactyly",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0021004",
  "properties": {
    "xrefs": [
      "DOID:0050581",
      "HP:0001156",
      "MEDGEN:67454",
      "MESH:D059327",
      "SCTID:43476002",
      "UMLS:C0221357",
      "icd11.foundation:598200019"
    ],
    "synonyms": [
      "brachydactyly",
      "brachydactyly (disease)"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "A disease characterized by the presence of brachydactyly, including syndromic and non-syndromic forms."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 22,
  "parents": [
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "id": 6893,
      "label": "skeletal system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4222
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0002461",
          "MEDGEN:538042",
          "SCTID:88230002",
          "UMLS:C0263661"
        ],
        "synonyms": [
          "disease of skeletal system",
          "disease or disorder of skeletal system",
          "disorder of skeletal system",
          "skeletal system disease",
          "skeletal system disease or disorder",
          "disease of bone and/or joint",
          "osteoarthropathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A disease involving the skeletal system."
      },
      "child_count": 48,
      "reference_id": "MONDO:0005172"
    },
    {
      "id": 20383,
      "label": "disorder of development or morphogenesis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29380
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD10CM:Q00-Q99",
          "MEDGEN:1843482",
          "UMLS:C0694457"
        ],
        "definition": "Any disease or disorder that disrupts the process development of an anatomical structure. Can be due to genetic or environmental causes. Typically happens during embryogenesis, but also includes post-embryonic development."
      },
      "child_count": 190,
      "reference_id": "MONDO:0021147"
    }
  ],
  "children": [
    {
      "id": 8546,
      "label": "Cooks syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18362,
        18956,
        20260
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0004083",
          "MEDGEN:354848",
          "MESH:C537766",
          "OMIM:106995",
          "Orphanet:1487",
          "SCTID:720747002",
          "UMLS:C1862841"
        ],
        "synonyms": [
          "Cooks syndrome",
          "ODP",
          "anonychia-onychodystrophy with hypoplasia or absence of distal phalanges syndrome",
          "anonychia and absence/hypoplasia of distal phalanges",
          "anonychia-onychodystrophy with hypoplasia or absence of distal phalanges"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Cooks syndrome is a malformation syndrome affecting the apical structures of digits and presenting with hypo/aplasia of nails and distal phalanges. More than half of digits are usually involved and the thumbs may appear digitalized."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007134"
    },
    {
      "id": 8616,
      "label": "brachydactyly-arterial hypertension syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4370,
        18362,
        18956,
        20260
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111247",
          "GARD:0000967",
          "MEDGEN:349445",
          "MESH:C537095",
          "OMIM:112410",
          "Orphanet:1276",
          "SCTID:720568003",
          "UMLS:C1862170"
        ],
        "synonyms": [
          "Bilginturan brachydactyly",
          "Bilginturan syndrome",
          "brachydactyly type E, with short stature and hypertension",
          "HTNB",
          "brachydactyly type E with short stature and hypertension",
          "brachydactyly with hypertension",
          "brachydactyly, type E, with short stature and hypertension",
          "hypertension and brachydactyly syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Brachydactyly - arterial hypertension is a rare genetic brachydactyly syndrome characterized by the association of brachydactyly type E with hypertension (due to vascular or neurovascular anomalies) as well as the additional features of short stature and low birth weight (compared to non-affected family members), stocky build and a round face. The onset of hypertension is often in childhood and, if untreated, most patients will have had a stroke by the age of 50."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007211"
    },
    {
      "id": 8618,
      "label": "Ballard syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20260
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110963",
          "GARD:0000959",
          "MEDGEN:349443",
          "MESH:C537094",
          "OMIM:112440",
          "Orphanet:93395",
          "SCTID:722298001",
          "UMLS:C1862163",
          "icd11.foundation:94436217"
        ],
        "synonyms": [
          "Pitt-Williams brachydactyly",
          "brachydactyly types B and E combined",
          "Pitt Williams brachydactyly",
          "brachydactyly Ballard type",
          "brachydactyly combined B and E types",
          "brachydactyly, Ballard type",
          "brachydactyly, combined B and E types"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Ballard syndrome is characterized by hypoplasia of the distal phalanges of the ulnar side of the hand and shortening of one or more metacarpals. In contrast to brachydactyly type E, patients with Ballard syndrome have normal stature."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007213"
    },
    {
      "id": 8620,
      "label": "brachydactyly type A1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20260,
        26116
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110964",
          "GARD:0000978",
          "MEDGEN:354673",
          "MESH:C537088",
          "OMIM:112500",
          "Orphanet:93388",
          "SCTID:715720006",
          "UMLS:C1862151",
          "icd11.foundation:568452529"
        ],
        "synonyms": [
          "BDA1",
          "brachydactyly, Farabee type",
          "Farabee-type brachydactyly",
          "brachydactyly Farabee type",
          "brachydactyly, type A1"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A rare, congenital limb malformation characterized by shortened or underdeveloped middle phalanges of all digits, that are sometimes fused with the terminal phalanges. The proximal phalanges of the thumbs and big toes are also shortened. Short stature in adulthood has been reported in association."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007215"
    },
    {
      "id": 8621,
      "label": "brachydactyly type A2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4370,
        20260
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110965",
          "GARD:0000979",
          "MEDGEN:318690",
          "MESH:C537089",
          "OMIM:112600",
          "Orphanet:93396",
          "SCTID:720569006",
          "UMLS:C1832702",
          "icd11.foundation:594491464"
        ],
        "synonyms": [
          "BDA2",
          "Mohr-Wriedt type brachydactyly",
          "brachydactyly, Mohr-Wriedt type",
          "Brachymesophalangy 2",
          "Brachymesophalangy type 2",
          "brachydactyly, type A2"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Brachydactyly type A2 (BDA2) is a congenital malformation characterized by shortening (hypoplasia or aplasia) of the middle phalanges of the index finger and, sometimes, of the little finger."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007216"
    },
    {
      "id": 8622,
      "label": "brachydactyly type A3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20260
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110966",
          "GARD:0027353",
          "MEDGEN:354670",
          "MESH:C537090",
          "OMIM:112700",
          "Orphanet:93393",
          "UMLS:C1862140",
          "icd11.foundation:153446585"
        ],
        "synonyms": [
          "BDA3",
          "brachydactyly-clinodactyly",
          "Brachymesophalangy 5",
          "brachydactyly, type A3"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0007217"
    },
    {
      "id": 8623,
      "label": "brachydactyly type A4",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20260
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110967",
          "GARD:0000990",
          "MEDGEN:354669",
          "MESH:C537097",
          "OMIM:112800",
          "Orphanet:93394",
          "SCTID:715721005",
          "UMLS:C1862139",
          "icd11.foundation:10379198"
        ],
        "synonyms": [
          "BDA4",
          "Brachymesophalangy II and V",
          "Temtamy type brachydactyly",
          "brachydactyly, Temtamy type",
          "brachymesophalangy II and V",
          "Brachymesophalangy 2 and 5",
          "brachydactyly Temtamy type",
          "brachydactyly, type A4"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Brachydactyly type A4 (BDA4) is a congenital malformation characterized by brachymesophalangy affecting mainly the 2nd and the 5th digit."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007218"
    },
    {
      "id": 8624,
      "label": "Osebold-Remondini syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19474,
        20260
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110968",
          "GARD:0000983",
          "MEDGEN:350598",
          "MESH:C537092",
          "OMIM:112910",
          "Orphanet:93382",
          "SCTID:715722003",
          "UMLS:C1862130"
        ],
        "synonyms": [
          "BDA6",
          "Osebold-Remondini syndrome",
          "brachydactyly type A6",
          "brachydactyly, type A6",
          "brachymesophalangy with mesomelic short limbs and carpal and tarsal osseous abnormalities",
          "Brachymesophalangy with mesomelic short limbs and carpal and tarsal osseous abnormalities",
          "OSEBOLD-Remondini syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A brachymesophalangy with mesomelic short limbs, and carpal and tarsal bone abnormalities. In general, the affected individuals are of slightly short stature and normal intelligence. The syndrome has been described in a kindred with seven affected members from three generations. Transmission appears to be autosomal dominant."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007219"
    },
    {
      "id": 8626,
      "label": "brachydactyly type C",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20260
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110970",
          "GARD:0000986",
          "MEDGEN:350590",
          "MESH:C537093",
          "OMIM:113100",
          "Orphanet:93384",
          "UMLS:C1862103",
          "icd11.foundation:956707061"
        ],
        "synonyms": [
          "brachydactyly type C",
          "brachydactyly Haws type",
          "brachydactyly, Haws type",
          "brachydactyly, type C"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0007221"
    },
    {
      "id": 8627,
      "label": "brachydactyly type D",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20260
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110971",
          "GARD:0027354",
          "MEDGEN:66313",
          "MESH:C562420",
          "OMIM:113200",
          "Orphanet:93385",
          "UMLS:C0220664",
          "icd11.foundation:642882691"
        ],
        "synonyms": [
          "BDD",
          "brachydactyly, type D",
          "stub thumb"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A brachydactyly characterized by short and broad terminal phalanges of the thumbs and big toes that has material basis in mutation in the HOXD13 gene on chromosome 2q31.1."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007222"
    },
    {
      "id": 8654,
      "label": "camptobrachydactyly",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20260
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0001062",
          "MEDGEN:349399",
          "MESH:C537967",
          "OMIM:114150",
          "Orphanet:1319",
          "SCTID:733045005",
          "UMLS:C1861963"
        ],
        "synonyms": [
          "camptobrachydactyly",
          "short foot/brachydactyly of toes, camptodactyly, brachydactyly"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Camptobrachydactyly is an extremely rare brachydactyly syndrome, characterized by short broad hands and feet with brachydactyly associated with congenital flexion contractures of the proximal and/or distal interphalangeal joints of the fingers, as well as syndactyly of feet. Polydactyly, septate vagina and urinary incontinence were also occasionally reported. Camptobrachydactyly has been described in 18 members of 1 family, suggesting an autosomal dominant inheritance. There have been no further descriptions in the literature since 1972."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007249"
    },
    {
      "id": 12843,
      "label": "brachydactyly type A1B",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20260
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110974",
          "GARD:0015407",
          "MEDGEN:339652",
          "MESH:C564635",
          "OMIM:607004",
          "UMLS:C1846949"
        ],
        "synonyms": [
          "BDA1B",
          "brachydactyly, type A1, B"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0011757"
    },
    {
      "id": 15042,
      "label": "brachydactyly type A1C",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20260
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110977",
          "GARD:0015903",
          "MEDGEN:767360",
          "OMIM:615072",
          "UMLS:C3554446"
        ],
        "synonyms": [
          "BDA1C",
          "GDF5 brachydactyly type A1",
          "brachydactyly type A1 caused by mutation in GDF5",
          "brachydactyly, type A1, C"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Any brachydactyly type A1 in which the cause of the disease is a mutation in the GDF5 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014032"
    },
    {
      "id": 15786,
      "label": "brachydactyly type A1D",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20260
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110978",
          "GARD:0016164",
          "MEDGEN:903193",
          "OMIM:616849",
          "UMLS:C4225183"
        ],
        "synonyms": [
          "BDA1D",
          "BMPR1B brachydactyly type A1",
          "brachydactyly type A1 caused by mutation in BMPR1B",
          "brachydactyly, type A1, D"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Any brachydactyly type A1 in which the cause of the disease is a mutation in the BMPR1B gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014798"
    },
    {
      "id": 17725,
      "label": "non-syndromic brachydactyly",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20260
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "Orphanet:294937"
        ],
        "synonyms": [
          "nonsyndromic brachydactyly",
          "brachydactyly",
          "isolated brachydactyly"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 3,
      "reference_id": "MONDO:0017424"
    },
    {
      "id": 19462,
      "label": "brachydactyly type B",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20260
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0000985",
          "MEDGEN:722046",
          "Orphanet:93383",
          "SCTID:389168002",
          "UMLS:C1300267",
          "icd11.foundation:1534264812"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A condition characterized by incomplete development (hypoplasia) or absence of the outermost bones of the fingers and toes (distal phalanges) and nails. Additional features may include hypoplasia of the middle phalanges, fusion of the joints (symphalangism), broad thumbs, and webbed fingers (syndactyly). The feet are often less severely affected than the hands. There are 2 types of this condition, designated as type 1 and 2. BDB type 1 is caused by mutations in the ROR2 gene. BDB type 2 is caused by mutations in the NOG gene. Inheritance of both types is autosomal dominant. Treatment may include surgery if the condition affects hand function, or for cosmetic reasons."
      },
      "child_count": 2,
      "reference_id": "MONDO:0019676"
    },
    {
      "id": 19463,
      "label": "brachydactyly type E",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20260
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0000987",
          "MEDGEN:939359",
          "Orphanet:93387",
          "UMLS:C4315392",
          "icd11.foundation:712007423"
        ],
        "synonyms": [
          "type E brachydactyly"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Brachydactyly type E (BDE) is a congenital malformation of the digits characterized by variable shortening of the metacarpals with more or less normal length phalanges, although the terminal phalanges are often short."
      },
      "child_count": 3,
      "reference_id": "MONDO:0019677"
    },
    {
      "id": 19464,
      "label": "brachydactyly type A5",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20260
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0000982",
          "MEDGEN:929661",
          "MESH:C537091",
          "OMIM:112900",
          "Orphanet:93389",
          "SCTID:720570007",
          "UMLS:C4303992",
          "icd11.foundation:291957825"
        ],
        "synonyms": [
          "absent middle phalanges of digits 2-5 with nail dysplasia",
          "brachydactyly type A5 nail dysplasia",
          "brachydactyly with absence of middle phalanges and hypoplastic nails"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Brachydactyly type A5 (BDA5) is a very rare congenital malformation of the digits characterized by absence of the middle phalanges (usually of digits 2 to 5), nail dysplasia and duplicated terminal phalanx of the thumb."
      },
      "child_count": 0,
      "reference_id": "MONDO:0019678"
    },
    {
      "id": 19465,
      "label": "brachydactyly type A7",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20260
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0000984",
          "MEDGEN:929660",
          "Orphanet:93397",
          "SCTID:720571006",
          "UMLS:C4303991",
          "icd11.foundation:1487696553"
        ],
        "synonyms": [
          "brachydactyly, Smorgasbord type",
          "brachydactyly Smorgasbord type"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Brachydactyly type A7 (Smorgasbord type) is a form of brachydactyly that presents with the characteristic features of brachydactyly type A2 (shortening of the middle phalanges of the index finger and, sometimes, of the little finger) and type D (shortening of the distal phalanx of the thumb) plus various additional features."
      },
      "child_count": 0,
      "reference_id": "MONDO:0019679"
    },
    {
      "id": 20108,
      "label": "brachydactyly type A1A",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20260
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025215"
        ],
        "synonyms": [
          "BDA1",
          "BRACHYDACTYLY, type A1",
          "Farabee-type Brachydactyly"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0020701"
    },
    {
      "id": 20800,
      "label": "Berk-Tabatznik syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20260
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0005109",
          "MEDGEN:443928",
          "MESH:C535432",
          "UMLS:C2930899"
        ],
        "synonyms": [
          "Berk Tabatznik syndrome",
          "cleft nare, brachydactyly, short stature dwarfism",
          "cleft nare, brachydactyly, short stature-dwarfism",
          "congenital optic atrophy and brachytelephalangy",
          "kyphosis brachyphalangy optic atrophy",
          "short stature, congenital optic atrophy, and hypoplasia of the cervical vertebral bodies and distal phalanges"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0021994"
    },
    {
      "id": 25272,
      "label": "preaxial digit brachydactyly-webbed fingers",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18362,
        20260
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026648",
          "MEDGEN:1843425",
          "Orphanet:633211",
          "UMLS:C5816807"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0859005"
    }
  ],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 6893,
      "label": "skeletal system disorder"
    },
    {
      "id": 20383,
      "label": "disorder of development or morphogenesis"
    }
  ]
}