{
  "id": 6735,
  "label": "cardiomyopathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0004994",
  "properties": {
    "xrefs": [
      "DOID:0050700",
      "EFO:0000318",
      "ICD10CM:I42",
      "ICD10WHO:I42",
      "ICD9:425",
      "ICD9:425.4",
      "ICD9:425.9",
      "MEDGEN:209232",
      "MESH:D009202",
      "MedDRA:10007636",
      "NCIT:C34830",
      "Orphanet:167848",
      "SCTID:85898001",
      "UMLS:C0878544",
      "icd11.foundation:282225286"
    ],
    "synonyms": [
      "Cardiomyopathies",
      "cardiomyopathy"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "A disease of the heart muscle or myocardium proper. Cardiomyopathies may be classified as either primary or secondary, on the basis of etiology, or on the pathophysiology of the lesion: hypertrophic, dilated, or restrictive."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 12,
  "parents": [
    {
      "id": 5798,
      "label": "muscle tissue disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4222
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080000",
          "DOID:66",
          "ICD10CM:M60-M63",
          "MESH:D009135"
        ],
        "synonyms": [
          "disease of muscle organ",
          "disease of muscle tissue",
          "disease or disorder of muscle organ",
          "disease or disorder of muscle tissue",
          "disorder of muscle organ",
          "disorder of muscle tissue",
          "muscle organ disease",
          "muscle organ disease or disorder",
          "muscle tissue disease",
          "muscle tissue disease or disorder",
          "muscular disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A disease involving the muscle tissue."
      },
      "child_count": 13,
      "reference_id": "MONDO:0003939"
    },
    {
      "id": 6967,
      "label": "heart disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6736
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:114",
          "EFO:0003777",
          "ICD9:429.89",
          "ICD9:429.9",
          "ICD9:V47.2",
          "MEDGEN:5458",
          "MESH:D006331",
          "NCIT:C3079",
          "SCTID:56265001",
          "UMLS:C0018799",
          "icd11.foundation:1512587470"
        ],
        "synonyms": [
          "cardiac disease",
          "disease of heart",
          "disease or disorder of heart",
          "disorder of heart",
          "disorder of heart/pericardium",
          "heart disease",
          "heart disease or disorder",
          "heart disorder",
          "heart trouble",
          "heart/pericardial disease",
          "heart/pericardial disease or disorder",
          "heart/pericardial disorder",
          "heart/pericardial trouble"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A disease involving the heart and/or pericardium."
      },
      "child_count": 34,
      "reference_id": "MONDO:0005267"
    }
  ],
  "children": [
    {
      "id": 2788,
      "label": "Keshan disease",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6735,
        7349,
        8312
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050083",
          "GARD:0008761",
          "ICD9:269.3",
          "MEDGEN:78639",
          "MESH:C536166",
          "SCTID:46939000",
          "UMLS:C0268095",
          "icd11.foundation:1307765114"
        ],
        "synonyms": [
          "congestive cardiomyopathy due to selenium deficiency",
          "enlarged heart and poor heart function"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A congestive cardiomyopathy caused by a combination of dietary deficiency of selenium and the presence of a mutated strain of Coxsackievirus."
      },
      "child_count": 0,
      "reference_id": "MONDO:0000241"
    },
    {
      "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"
    },
    {
      "id": 4846,
      "label": "extrinsic cardiomyopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6735
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3978",
          "GARD:0023255",
          "ICD9:425.8",
          "MEDGEN:739084",
          "SCTID:195029002",
          "UMLS:C1689817"
        ],
        "synonyms": [
          "secondary cardiomyopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A cardiomyopathy that is not due to abnormalities in heart muscle cells."
      },
      "child_count": 1,
      "reference_id": "MONDO:0002824"
    },
    {
      "id": 6836,
      "label": "idiopathic cardiomyopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6735,
        24405
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0000767",
          "GARD:0024149",
          "MEDGEN:18634",
          "NCIT:C53654",
          "UMLS:C0033141"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A disease of the heart muscle or myocardium proper whose cause is unknown."
      },
      "child_count": 4,
      "reference_id": "MONDO:0005110"
    },
    {
      "id": 6933,
      "label": "familial cardiomyopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6735,
        24272
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0002945",
          "GARD:0024166",
          "ICD9:425.4",
          "MEDGEN:538845",
          "SCTID:35728003",
          "UMLS:C0264789",
          "icd11.foundation:1018022925"
        ],
        "synonyms": [
          "hereditary cardiomyopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "An instance of cardiomyopathy that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 18,
      "reference_id": "MONDO:0005217"
    },
    {
      "id": 7091,
      "label": "non-compaction cardiomyopathy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6735
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0004686",
          "GARD:0024182",
          "MEDGEN:1843481",
          "UMLS:C4324548"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Left ventricular non-compaction (LVNC) is characterized by prominent left ventricular trabeculae and deep inter-trabecular recesses. The myocardial wall is often thickened with a thin, compacted epicardial layer and a thickened endocardial layer. In some patients, LVNC is associated with left ventricular dilatation and systolic dysfunction, which can be transient in neonates."
      },
      "child_count": 0,
      "reference_id": "MONDO:0005418"
    },
    {
      "id": 7147,
      "label": "Chagas cardiomyopathy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6735,
        20718
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0005529",
          "GARD:0024193",
          "ICD9:086.0",
          "MEDGEN:868",
          "MESH:D002598",
          "SCTID:998008",
          "UMLS:C0007930"
        ],
        "synonyms": [
          "Trypanosoma cruzi cardiomyopathy",
          "Trypanosoma cruzi caused cardiomyopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A disease of the cardiac muscle developed subsequent to the initial protozoan infection by trypanosoma cruzi. After infection, less than 10% develop acute illness such as myocarditis (mostly in children). The disease then enters a latent phase without clinical symptoms until about 20 years later. Myocardial symptoms of advanced chagas disease include conduction defects (heart block) and cardiomegaly."
      },
      "child_count": 0,
      "reference_id": "MONDO:0005491"
    },
    {
      "id": 18244,
      "label": "Uhl anomaly",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6735
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0005393",
          "MEDGEN:78576",
          "MESH:C536932",
          "MedDRA:10048951",
          "Orphanet:3403",
          "UMLS:C0265857",
          "icd11.foundation:240652322"
        ],
        "synonyms": [
          "Uhl's anomaly",
          "parchment right ventricle"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Uhl anomaly is characterized by an almost complete absence of the myocardium in the right ventricle resulting in a thin walled nonfunctional right ventricle manifesting with cardiac arrhythmias and right ventricular failure. Cases of partial absence of right ventricular myocardium which remains asymptomatic or mildly symptomatic until adulthood have also been reported. Patients presenting with complete Uhl anomaly should be considered for cardiac transplantation."
      },
      "child_count": 0,
      "reference_id": "MONDO:0018084"
    },
    {
      "id": 18932,
      "label": "Tako-tsubo cardiomyopathy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6735
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:1002000",
          "GARD:0009400",
          "ICD10CM:I51.81",
          "ICD9:429.83",
          "MEDGEN:366029",
          "MESH:D054549",
          "NCIT:C85181",
          "NORD:2006",
          "Orphanet:66529",
          "SCTID:441541008",
          "UMLS:C1739395",
          "icd11.foundation:478139552"
        ],
        "synonyms": [
          "Tako-Tsubo syndrome",
          "Takotsubo Cardiomyopathy",
          "Takotsubo cardiomyopathy",
          "Takotsubo syndrome",
          "ampulla cardiomyopathy",
          "apical ballooning syndrome",
          "ballooning cardiomyopathy",
          "broken heart syndrome",
          "stress cardiomyopathy",
          "transient left ventricular apical ballooning syndrome",
          "ASC",
          "Tako tsubo syndrome",
          "acute stress cardiomyopathy",
          "broken-heart syndrome",
          "left ventricular transient apical ballooning",
          "stress-induced cardiomyopathy",
          "transient antero-apical dyskinesia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Takotsubo cardiomyopathy (TC) is a recently described acute cardiac syndrome that mimics acute myocardial infarction and is characterized by ischemic chest symptoms, an elevated ST segment on electrocardiogram, and elevated levels of cardiac disease markers."
      },
      "child_count": 0,
      "reference_id": "MONDO:0019018"
    },
    {
      "id": 20929,
      "label": "cardiomyopathy due to anthracyclines",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6735
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0001107",
          "MEDGEN:1755373",
          "UMLS:C5437452"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0022653"
    },
    {
      "id": 21092,
      "label": "doxorubicin induced cardiomyopathy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6735
      ],
      "type_id": 0,
      "properties": {
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0023006"
    },
    {
      "id": 22008,
      "label": "autoimmune cardiomyopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3005,
        3017,
        6735
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0040095",
          "GARD:0025617"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An autoimmune form of cardiomyopathy."
      },
      "child_count": 3,
      "reference_id": "MONDO:0030701"
    }
  ],
  "roots": [
    {
      "id": 5798,
      "label": "muscle tissue disorder"
    },
    {
      "id": 6967,
      "label": "heart disorder"
    }
  ]
}