{
  "id": 19848,
  "label": "double outlet right ventricle with non-committed subpulmonary ventricular septal defect",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020388",
  "properties": {
    "xrefs": [
      "GARD:0019617",
      "MEDGEN:365501",
      "Orphanet:99046",
      "UMLS:C1956410",
      "icd11.foundation:2032277111"
    ],
    "synonyms": [
      "DORV with non-committed subpulmonary VSD"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18249,
      "label": "double outlet right ventricle",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4213,
        17072
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:6406",
          "GARD:0001908",
          "ICD10CM:Q20.1",
          "MEDGEN:41649",
          "MESH:D004310",
          "MedDRA:10013611",
          "NANDO:1200710",
          "NANDO:2100076",
          "NANDO:2200256",
          "NCIT:C98916",
          "Orphanet:3426",
          "SCTID:204299009",
          "UMLS:C0013069",
          "icd11.foundation:141717788"
        ],
        "synonyms": [
          "DORV",
          "double outlet right ventricle"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Double outlet right ventricle (DORV) is a rare cono-truncal anomaly in which both the aorta and pulmonary artery originate, either entirely or predominantly, from the morphologic right ventricle."
      },
      "child_count": 10,
      "reference_id": "MONDO:0018089"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18249,
      "label": "double outlet right ventricle"
    }
  ]
}