{
  "id": 10262,
  "label": "heart defect - tongue hamartoma - polysyndactyly syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009008",
  "properties": {
    "xrefs": [
      "DOID:0111591",
      "GARD:0004166",
      "MEDGEN:341804",
      "MESH:C535849",
      "OMIM:217085",
      "Orphanet:1338",
      "UMLS:C1857587"
    ],
    "synonyms": [
      "Ostravik-Lindemann-Solberg syndrome",
      "heart defect - tongue hamartoma - polysyndactyly syndrome",
      "CHDTHP",
      "Orstavik Lindemann Solberg syndrome",
      "congenital heart defects, hamartomas of tongue, and polysyndactyly",
      "heart defect, tongue hamartoma and polysyndactyly"
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "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"
    },
    {
      "id": 24751,
      "label": "WDPCP-related ciliopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7000
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0028033"
        ],
        "synonyms": [
          "WDPCP-related ciliopathy"
        ],
        "definition": "Any ciliopathy caused by variants in the WDPCP gene, including cases diagnosed as Bardet-Biedl syndrome 15 or congenital heart defects, hamartomas of tongue, and polysyndactyly."
      },
      "child_count": 2,
      "reference_id": "MONDO:0700378"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16089,
      "label": "multiple congenital anomalies/dysmorphic syndrome without intellectual disability"
    },
    {
      "id": 24751,
      "label": "WDPCP-related ciliopathy"
    }
  ]
}