{
  "id": 12505,
  "label": "dilated cardiomyopathy 1G",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011400",
  "properties": {
    "xrefs": [
      "DOID:0110430",
      "GARD:0015363",
      "MEDGEN:347714",
      "MESH:C565824",
      "OMIM:604145",
      "UMLS:C1858763"
    ],
    "synonyms": [
      "CMD1G",
      "TTN familial isolated dilated cardiomyopathy",
      "cardiomyopathy, dilated, type 1G",
      "dilated cardiomyopathy type 1G",
      "familial isolated dilated cardiomyopathy caused by mutation in TTN",
      "cardiomyopathy, dilated, 1G"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the TTN gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "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"
    },
    {
      "id": 24709,
      "label": "familial isolated dilated cardiomyopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16878
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027293",
          "MEDGEN:1826005",
          "Orphanet:154",
          "UMLS:C5679590",
          "icd11.foundation:949016860"
        ],
        "synonyms": [
          "familial isolated dilated cardiomyopathy",
          "familial or idiopathic dilated cardiomyopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A rare familial cardiomyopathy characterized by the dilation of left ventricle and progressively impairing of systolic ventricular function, in the absence of abnormal loading conditions or coronary artery disease sufficient to cause global systolic impairment. The disease may cause heart failure or arrhythmia. The disease is isolated when no additional atypical cardiac or extracardiac manifestations are present."
      },
      "child_count": 45,
      "reference_id": "MONDO:0700335"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 24220,
      "label": "autosomal dominant titinopathy"
    },
    {
      "id": 24709,
      "label": "familial isolated dilated cardiomyopathy"
    }
  ]
}