{
  "id": 14444,
  "label": "hypertrophic cardiomyopathy 9",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013412",
  "properties": {
    "xrefs": [
      "DOID:0110315",
      "GARD:0024921",
      "MEDGEN:348780",
      "MESH:C566044",
      "OMIM:613765",
      "UMLS:C1861065"
    ],
    "synonyms": [
      "CMH9",
      "TTN hypertrophic cardiomyopathy",
      "cardiomyopathy, familial hypertrophic, 9",
      "cardiomyopathy, familial hypertrophic, type 9",
      "hypertrophic cardiomyopathy caused by mutation in TTN",
      "hypertrophic cardiomyopathy type 9"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TTN 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"
    },
    {
      "id": 24220,
      "label": "autosomal dominant titinopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        23917
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026247"
        ],
        "synonyms": [
          "TTN-related myopathy, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Autosomal dominant form of TTN-related myopathy."
      },
      "child_count": 8,
      "reference_id": "MONDO:0100494"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 21518,
      "label": "familial hypertrophic cardiomyopathy"
    },
    {
      "id": 24220,
      "label": "autosomal dominant titinopathy"
    }
  ]
}