{
  "id": 15042,
  "label": "brachydactyly type A1C",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014032",
  "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."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 20260,
      "label": "brachydactyly",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6893,
        20383
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 66,
      "reference_id": "MONDO:0021004"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 20260,
      "label": "brachydactyly"
    }
  ]
}