{
  "id": 9805,
  "label": "syndactyly type 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008514",
  "properties": {
    "xrefs": [
      "DOID:0111817",
      "GARD:0005088",
      "MEDGEN:396117",
      "MESH:C538154",
      "OMIM:186100",
      "Orphanet:93404",
      "SCTID:715725001",
      "UMLS:C1861366",
      "icd11.foundation:144846004"
    ],
    "synonyms": [
      "GJA1 non-syndromic syndactyly",
      "SD3",
      "non-syndromic syndactyly caused by mutation in GJA1",
      "syndactyly of fingers 4 and 5",
      "Ring and Little finger syndactyly",
      "Sdty3",
      "syndactyly of fingers four and five",
      "syndactyly of the ring and little finger",
      "syndactyly, type 3",
      "syndactyly, type III"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "Syndactyly type 3 (SD3) is a rare congenital distal limb malformation characterized by complete and bilateral syndactyly between the 4th and 5th fingers."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19340,
      "label": "non-syndromic syndactyly",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20258
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1842957",
          "MedDRA:10042778",
          "NCIT:C87125",
          "Orphanet:90025",
          "UMLS:C5681365",
          "icd11.foundation:1736296640"
        ],
        "synonyms": [
          "nonsyndromic syndactyly",
          "chromosome 2q35 duplication syndrome",
          "isolated syndactyly",
          "symphalangism",
          "symphalangy",
          "syndactyly",
          "webbing of digits"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A congenital condition characterized by webbing between the fingers and/or toes, joining the digits together. In rare cases, the joining of the fingers or toes may involve bony fusion between the digits. Common causes include Down Syndrome and hereditary syndactyly."
      },
      "child_count": 8,
      "reference_id": "MONDO:0019530"
    },
    {
      "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": 19340,
      "label": "non-syndromic syndactyly"
    },
    {
      "id": 24804,
      "label": "polydactyly-syndactyly-triphalangism"
    }
  ]
}