{
  "id": 15806,
  "label": "autosomal dominant Robinow syndrome 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014819",
  "properties": {
    "xrefs": [
      "DOID:0060767",
      "GARD:0018549",
      "MEDGEN:907878",
      "OMIM:616894",
      "UMLS:C4225164"
    ],
    "synonyms": [
      "DRS3",
      "DVL3 Robinow syndrome",
      "Robinow syndrome caused by mutation in DVL3",
      "Robinow syndrome, autosomal dominant 3",
      "Robinow syndrome, autosomal dominant type 3",
      "autosomal dominant Robinow syndrome type 3"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Any Robinow syndrome in which the cause of the disease is a mutation in the DVL3 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 9688,
      "label": "autosomal dominant Robinow syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        19689
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016620",
          "ICD9:759.89",
          "MEDGEN:1675001",
          "Orphanet:3107",
          "SCTID:76520005",
          "UMLS:C5200540",
          "icd11.foundation:807338758"
        ],
        "synonyms": [
          "Robinow syndrome, autosomal dominant",
          "Robinow syndrome, autosomal dominant type",
          "autosomal dominant Robinow syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Autosomal dominant Robinow syndrome (DRS) is the more common type of Robinow syndrome (RS) characterized by mild to moderate limb shortening and abnormalities of the head, face and external genitalia."
      },
      "child_count": 6,
      "reference_id": "MONDO:0008389"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 9688,
      "label": "autosomal dominant Robinow syndrome"
    }
  ]
}