{
  "id": 13177,
  "label": "hypertrophic cardiomyopathy 8",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012111",
  "properties": {
    "xrefs": [
      "DOID:0110314",
      "GARD:0024842",
      "MEDGEN:324806",
      "MESH:C563866",
      "OMIM:608751",
      "UMLS:C1837471"
    ],
    "synonyms": [
      "MYL3 hypertrophic cardiomyopathy",
      "cardiomyopathy, familial hypertrophic, 8",
      "cardiomyopathy, familial hypertrophic, type 8",
      "cardiomyopathy, hypertrophic, 8",
      "hypertrophic cardiomyopathy 8",
      "hypertrophic cardiomyopathy caused by mutation in MYL3",
      "hypertrophic cardiomyopathy type 8",
      "CMH8",
      "cardiomyopathy, hypertrophic, mid-left ventricular chamber type, 1"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYL3 gene."
  },
  "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"
    }
  ]
}