{
  "id": 18244,
  "label": "Uhl anomaly",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018084",
  "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."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 6735,
      "label": "cardiomyopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5798,
        6967
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 24,
      "reference_id": "MONDO:0004994"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6735,
      "label": "cardiomyopathy"
    }
  ]
}