{
  "id": 9928,
  "label": "hypertrophic cardiomyopathy 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008647",
  "properties": {
    "xrefs": [
      "DOID:0110307",
      "GARD:0024636",
      "MEDGEN:501195",
      "OMIM:192600",
      "UMLS:C3495498"
    ],
    "synonyms": [
      "CMH1",
      "MYH7 hypertrophic cardiomyopathy",
      "cardiomyopathy, familial hypertrophic, Autosomal dominant, Digenic dominant",
      "cardiomyopathy, familial hypertrophic, type 1",
      "cardiomyopathy, hypertrophic, 1, Autosomal dominant, Digenic dominant",
      "cardiomyopathy, hypertrophic, 1, digenic, Autosomal dominant, Digenic dominant",
      "hypertrophic cardiomyopathy 1",
      "hypertrophic cardiomyopathy caused by mutation in MYH7",
      "hypertrophic cardiomyopathy type 1",
      "Cmh",
      "asymmetric septal Hypertrophy",
      "cardiomyopathy, familial hypertrophic, 1",
      "hypertrophic subaortic stenosis, idiopathic",
      "ventricular Hypertrophy, hereditary"
    ],
    "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 MYH7 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"
    }
  ]
}