{
  "id": 11697,
  "label": "dilated cardiomyopathy 3B",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010542",
  "properties": {
    "xrefs": [
      "DOID:0060561",
      "DOID:0081164",
      "DOID:0110461",
      "GARD:0015287",
      "ICD9:425.4",
      "MEDGEN:777148",
      "MESH:C580047",
      "OMIM:302045",
      "SCTID:702424003",
      "UMLS:C3668940"
    ],
    "synonyms": [
      "CMD3B",
      "DMD dilated cardiomyopathy",
      "cardiomyopathy, dilated, type 3B",
      "dilated cardiomyopathy 3B",
      "dilated cardiomyopathy caused by mutation in DMD",
      "dilated cardiomyopathy type 3B",
      "DMD-related dilated cardiomyopathy",
      "X-linked dilated cardiomyopathy",
      "cardiomyopathy, dilated, 3B",
      "cardiomyopathy, dilated, X-linked"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any dilated cardiomyopathy in which the cause of the disease is a mutation in the DMD gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16752,
      "label": "neuromuscular disease caused by qualitative or quantitative defects of dystrophin",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16744
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0002031",
          "MEDGEN:1826053",
          "NANDO:1200487",
          "Orphanet:207085",
          "UMLS:C5679787"
        ],
        "synonyms": [
          "dystrophinopathy",
          "qualitative or quantitative defects of dystrophin"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0016147"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6799
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "neurogenetic disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology characterized by abnormalities in the brain, spinal cord, nerves, or muscles."
      },
      "child_count": 528,
      "reference_id": "MONDO:0100545"
    },
    {
      "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": 16752,
      "label": "neuromuscular disease caused by qualitative or quantitative defects of dystrophin"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    },
    {
      "id": 24709,
      "label": "familial isolated dilated cardiomyopathy"
    }
  ]
}