{
  "id": 12584,
  "label": "dilated cardiomyopathy 1I",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011482",
  "properties": {
    "xrefs": [
      "DOID:0110431",
      "GARD:0015372",
      "MEDGEN:387998",
      "MESH:C565752",
      "OMIM:604765",
      "UMLS:C1858154"
    ],
    "synonyms": [
      "CMD1I",
      "DES familial isolated dilated cardiomyopathy",
      "cardiomyopathy, dilated, type 1I",
      "dilated cardiomyopathy type 1I",
      "familial isolated dilated cardiomyopathy caused by mutation in DES",
      "cardiomyopathy, dilated, 1I"
    ],
    "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 DES gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16774,
      "label": "qualitative or quantitative defects of desmin",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16773,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020426",
          "MEDGEN:1842905",
          "Orphanet:209041",
          "UMLS:C5680839"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 10,
      "reference_id": "MONDO:0016187"
    },
    {
      "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": 16774,
      "label": "qualitative or quantitative defects of desmin"
    },
    {
      "id": 24709,
      "label": "familial isolated dilated cardiomyopathy"
    }
  ]
}