{
  "id": 6757,
  "label": "dilated cardiomyopathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0005021",
  "properties": {
    "xrefs": [
      "DOID:12930",
      "EFO:0000407",
      "GARD:0000221",
      "HP:0001644",
      "ICD10CM:I42.0",
      "ICD9:425.4",
      "MEDGEN:2880",
      "MESH:D002311",
      "MedDRA:10056370",
      "NANDO:2100057",
      "NANDO:2200232",
      "NCIT:C84673",
      "Orphanet:217604",
      "SCTID:195021004",
      "UMLS:C0007193",
      "icd11.foundation:1916294688"
    ],
    "synonyms": [
      "dilated cardiomyopathy",
      "familial dilated cardiomyopathy",
      "idiopathic dilation cardiomyopathy",
      "primary dilated cardiomyopathy"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "Cardiomyopathy which is characterized by dilation and contractile dysfunction of the left and right ventricles. It may be idiopathic, or it may result from a myocardial infarction, myocardial infection, or alcohol abuse. It is a cause of congestive heart failure."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 3007,
      "label": "intrinsic cardiomyopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6735
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060036",
          "GARD:0022809"
        ],
        "synonyms": [
          "intrinsic cardiomyopathy",
          "primary cardiomyopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A cardiomyopathy that is due to abnormalities in heart muscle cells."
      },
      "child_count": 6,
      "reference_id": "MONDO:0000591"
    }
  ],
  "children": [
    {
      "id": 6918,
      "label": "viral dilated cardiomyopathy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6757,
        20721
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0002629",
          "GARD:0024162",
          "MEDGEN:538852",
          "SCTID:30496006",
          "UMLS:C0264797",
          "Wikipedia:Viral_cardiomyopathy"
        ],
        "synonyms": [
          "Viruses caused dilated cardiomyopathy",
          "Viruses dilated cardiomyopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "An dilated cardiomyopathy caused by infection with Viruses."
      },
      "child_count": 0,
      "reference_id": "MONDO:0005200"
    },
    {
      "id": 16878,
      "label": "familial dilated cardiomyopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6757,
        6933
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020525",
          "MEDGEN:90951",
          "MESH:C536231",
          "OMIMPS:115200",
          "Orphanet:217607",
          "UMLS:C0340427",
          "icd11.foundation:423719003"
        ],
        "synonyms": [
          "hereditary dilated cardiomyopathy",
          "DCM",
          "dilated cardiomyopathy, familial",
          "hypokinetic dilated cardiomyopathy, familial",
          "idiopathic dilated cardiomyopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A a genetic form of heart disease that occurs when heart (cardiac) muscle becomes thin and weakened in at least one chamber of the heart, causing the open area of the chamber to become enlarged (dilated). As a result, the heart is unable to pump blood as efficiently as usual. To compensate, the heart attempts to increase the amount of blood being pumped through the heart, leading to further thinning and weakening of the cardiac muscle. Over time, this condition results in heart failure."
      },
      "child_count": 58,
      "reference_id": "MONDO:0016333"
    },
    {
      "id": 16879,
      "label": "non-familial dilated cardiomyopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6757
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020530",
          "MEDGEN:1843057",
          "Orphanet:217629",
          "UMLS:C5681849",
          "icd11.foundation:1782708952"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0016338"
    }
  ],
  "roots": [
    {
      "id": 3007,
      "label": "intrinsic cardiomyopathy"
    }
  ]
}