{
  "id": 16879,
  "label": "non-familial dilated cardiomyopathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016338",
  "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"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 6757,
      "label": "dilated cardiomyopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3007
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 3,
      "reference_id": "MONDO:0005021"
    }
  ],
  "children": [
    {
      "id": 18844,
      "label": "peripartum cardiomyopathy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16879,
        21520
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9997",
          "EFO:0002628",
          "GARD:0000220",
          "ICD10CM:O90.3",
          "ICD9:674.5",
          "ICD9:674.54",
          "MEDGEN:163756",
          "MedDRA:10049430",
          "NCIT:C171602",
          "Orphanet:563",
          "SCTID:62377009",
          "UMLS:C0877208",
          "icd11.foundation:1218807936"
        ],
        "synonyms": [
          "peripartum cardiomyopathy",
          "postpartum cardiomyopathy",
          "Meadows' syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Peripartum cardiomyopathy (PPCM) is an idiopathic, potentially fatal form of dilated cardiomyopathy that develops during the final month of pregnancy or within five months after delivery."
      },
      "child_count": 0,
      "reference_id": "MONDO:0018920"
    },
    {
      "id": 18855,
      "label": "cirrhotic cardiomyopathy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16875,
        16879
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018852",
          "MEDGEN:1391593",
          "Orphanet:57777",
          "SCTID:725416005",
          "UMLS:C4511053",
          "icd11.foundation:1268082489"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Cirrhotic cardiomyopathy is the term used to describe a constellation of features indicative of abnormal heart structure and function in patients with cirrhosis. These include systolic and diastolic dysfunction, electrophysiological changes, and macroscopic and microscopic structural changes."
      },
      "child_count": 0,
      "reference_id": "MONDO:0018932"
    }
  ],
  "roots": [
    {
      "id": 6757,
      "label": "dilated cardiomyopathy"
    }
  ]
}