{
  "id": 8670,
  "label": "hypertrophic cardiomyopathy 4",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007268",
  "properties": {
    "xrefs": [
      "DOID:0110310",
      "GARD:0024542",
      "MEDGEN:350526",
      "MESH:C566169",
      "NCIT:C133725",
      "OMIM:115197",
      "UMLS:C1861862"
    ],
    "synonyms": [
      "CMH4",
      "MYBPC3 hypertrophic cardiomyopathy",
      "cardiomyopathy, familial hypertrophic, 4",
      "cardiomyopathy, familial hypertrophic, type 4",
      "cardiomyopathy, hypertrophic, 4",
      "familial hypertrophic cardiomyopathy type 4",
      "hypertrophic cardiomyopathy 4",
      "hypertrophic cardiomyopathy caused by mutation in MYBPC3",
      "hypertrophic cardiomyopathy type 4",
      "cardiomyopathy, familial hypertrophic, 4, susceptibility to"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "An autosomal dominant condition caused by mutation(s) in the MYBPC3 gene, encoding MYBPC3 protein. It is characterized by severe neonatal hypertrophic cardiomyopathy."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 21518,
      "label": "familial hypertrophic cardiomyopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6777,
        6933
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080326",
          "MEDGEN:183649",
          "MESH:D024741",
          "NCIT:C84773",
          "OMIMPS:192600",
          "Orphanet:155",
          "SCTID:471885006",
          "UMLS:C0949658",
          "icd11.foundation:1408928442"
        ],
        "synonyms": [
          "cardiomyopathy, familial hypertrophic",
          "familial hypertrophic cardiomyopathy",
          "familila or idiopathic hypertrophic obstructive cardiomyopathy",
          "hereditary hypertrophic cardiomyopathy",
          "hypertrophic familial cardiomyopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Hypertrophic cardiomyopathy caused by mutations in the genes encoding components of the sarcomere, in the absence of predisposing conditions."
      },
      "child_count": 80,
      "reference_id": "MONDO:0024573"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 21518,
      "label": "familial hypertrophic cardiomyopathy"
    }
  ]
}