{
  "id": 9804,
  "label": "synpolydactyly type 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008513",
  "properties": {
    "xrefs": [
      "GARD:0017358",
      "MEDGEN:1809573",
      "OMIM:186000",
      "Orphanet:295195",
      "UMLS:C5574994",
      "icd11.foundation:1701170393"
    ],
    "synonyms": [
      "HOXD13 non-syndromic synpolydactyly",
      "SD2, Vordingborg type",
      "SD2a",
      "SPD, Vordingborg type",
      "SPD1",
      "non-syndromic synpolydactyly caused by mutation in HOXD13",
      "synpolydactyly type 1",
      "synpolydactyly, Vordingborg type",
      "syndactyly, type 2",
      "synpolydactyly 1",
      "synpolydactyly with foot anomalies"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "Any non-syndromic synpolydactyly in which the cause of the disease is a mutation in the HOXD13 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3103,
      "label": "non-syndromic synpolydactyly",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19340,
        20703
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060242",
          "GARD:0022819"
        ],
        "synonyms": [
          "isolated synpolydactyly",
          "nonsyndromic synpolydactyly",
          "synpolydactyly"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A synpolydactyly that is not part of a larger syndrome."
      },
      "child_count": 8,
      "reference_id": "MONDO:0000722"
    },
    {
      "id": 12458,
      "label": "non-syndromic polydactyly",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20259
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MedDRA:10036063",
          "Orphanet:2913",
          "icd11.foundation:1534380955"
        ],
        "synonyms": [
          "isolated polydactyly (disease)",
          "nonsyndromic polydactyly",
          "nonsyndromic polydactyly (disease)",
          "Extra digits",
          "isolated polydactyly",
          "polydactylia",
          "supernumerary digits"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A congenital anomaly of the hand or foot, marked by the presence of supernumerary digits."
      },
      "child_count": 10,
      "reference_id": "MONDO:0011348"
    },
    {
      "id": 24804,
      "label": "polydactyly-syndactyly-triphalangism",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18360,
        20258,
        20259
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026428"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Any skeletal dysplasia that is characterizedby polydactyly, syndactyly and triphalangism, where a digit has three phalanges instead of two."
      },
      "child_count": 84,
      "reference_id": "MONDO:0800066"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3103,
      "label": "non-syndromic synpolydactyly"
    },
    {
      "id": 12458,
      "label": "non-syndromic polydactyly"
    },
    {
      "id": 24804,
      "label": "polydactyly-syndactyly-triphalangism"
    }
  ]
}