{
  "id": 25837,
  "label": "Greig cephalopolysyndactyly-contiguous gene syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0958130",
  "properties": {
    "xrefs": [
      "GARD:0026945",
      "MEDGEN:1864335",
      "Orphanet:658805",
      "UMLS:C5925145"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 9593,
      "label": "Greig cephalopolysyndactyly syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        24804
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:14761",
          "GARD:0006550",
          "MEDGEN:120531",
          "MESH:C537300",
          "MedDRA:10053878",
          "NCIT:C35255",
          "NORD:1206",
          "OMIM:175700",
          "Orphanet:380",
          "SCTID:32985001",
          "UMLS:C0265306",
          "icd11.foundation:606500237"
        ],
        "synonyms": [
          "GCPS",
          "Greig cephalopolysyndactyly syndrome",
          "Greig cephalosyndactyly syndrome",
          "Greig's syndrome",
          "Greig syndrome",
          "polysyndactyly with peculiar skull Shape"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Greig cephalopolysyndactyly syndrome (GCPS) is a pleiotropic, multiple congenital anomaly syndrome."
      },
      "child_count": 2,
      "reference_id": "MONDO:0008287"
    },
    {
      "id": 16089,
      "label": "multiple congenital anomalies/dysmorphic syndrome without intellectual disability",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18951
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019833",
          "MEDGEN:1842829",
          "Orphanet:102285",
          "UMLS:C5680373"
        ],
        "synonyms": [
          "MCA without intellectual disability",
          "multiple congenital anomalies without intellectual disability with or without dysmorphism"
        ]
      },
      "child_count": 168,
      "reference_id": "MONDO:0015161"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 9593,
      "label": "Greig cephalopolysyndactyly syndrome"
    },
    {
      "id": 16089,
      "label": "multiple congenital anomalies/dysmorphic syndrome without intellectual disability"
    }
  ]
}