{
  "id": 6919,
  "label": "restrictive cardiomyopathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0005201",
  "properties": {
    "xrefs": [
      "DOID:397",
      "EFO:0002630",
      "GARD:0020531",
      "ICD9:425.4",
      "MEDGEN:40111",
      "MESH:D002313",
      "MedDRA:10038748",
      "NANDO:1200292",
      "NANDO:1200293",
      "NANDO:2100058",
      "NANDO:2200233",
      "NCIT:C62798",
      "Orphanet:217632",
      "SCTID:415295002",
      "UMLS:C0007196",
      "icd11.foundation:316495940"
    ],
    "synonyms": [
      "restrictive cardiomyopathy",
      "familial restrictive cardiomyopathy"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "A type of heart disorder referring to the inability of the ventricles to fill with blood because the myocardium (heart muscle) stiffens and looses its flexibility. Causes include replacement of the myocardium with scar tissue, abnormal cellular infiltration of the myocardium, or deposition of a substance (e.g., amyloid) in the myocardium."
  },
  "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": 8203,
      "label": "endomyocardial fibrosis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6919
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12932",
          "EFO:1000921",
          "GARD:0006340",
          "ICD9:425.0",
          "MEDGEN:107513",
          "MESH:D004719",
          "MedDRA:10014800",
          "NCIT:C34585",
          "NORD:1092",
          "UMLS:C0553980",
          "icd11.foundation:365224859"
        ],
        "synonyms": [
          "African endomyocardial fibrosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A disease characterized by fibrotic thickening of the endocardium, particularly the right and/or left inflow tracts. The disease often involves the atrioventricular valves, leading to valvular regurgitaion. It most commonly occurs in children living within 15 degrees of the equator."
      },
      "child_count": 0,
      "reference_id": "MONDO:0006746"
    },
    {
      "id": 16880,
      "label": "familial restrictive cardiomyopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6919,
        6933
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020532",
          "ICD9:425.4",
          "MEDGEN:468561",
          "OMIMPS:115210",
          "Orphanet:217635",
          "SCTID:233878008",
          "UMLS:C0340429"
        ],
        "synonyms": [
          "hereditary restrictive cardiomyopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "An instance of restrictive cardiomyopathy that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 20,
      "reference_id": "MONDO:0016340"
    },
    {
      "id": 16883,
      "label": "non-familial restrictive cardiomyopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6919
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020535",
          "MEDGEN:1843079",
          "NANDO:1200294",
          "Orphanet:217720",
          "UMLS:C5680885",
          "icd11.foundation:2097520643"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 7,
      "reference_id": "MONDO:0016345"
    }
  ],
  "roots": [
    {
      "id": 3007,
      "label": "intrinsic cardiomyopathy"
    }
  ]
}