{
  "id": 15346,
  "label": "congenital heart defects, multiple types, 4",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014344",
  "properties": {
    "xrefs": [
      "GARD:0024987",
      "MEDGEN:862747",
      "OMIM:615779",
      "UMLS:C4014310"
    ],
    "synonyms": [
      "NR2F2 congenital heart defects, multiple types",
      "congenital heart defects, multiple types caused by mutation in NR2F2",
      "congenital heart defects, multiple types, 4",
      "CHTD4"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "Any congenital heart defects, multiple types in which the cause of the disease is a mutation in the NR2F2 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2732,
      "label": "congenital heart defects, multiple types",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7116
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "CHTD"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 8,
      "reference_id": "MONDO:0000119"
    },
    {
      "id": 19775,
      "label": "familial atrioventricular septal defect",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4221,
        24272
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050651",
          "GARD:0000802",
          "ICD10CM:Q21.2",
          "ICD9:745.6",
          "ICD9:745.60",
          "ICD9:745.69",
          "NCIT:C101029",
          "NORD:821",
          "OMIMPS:606215",
          "Orphanet:98722",
          "SCTID:15459006"
        ],
        "synonyms": [
          "Atrioventricular Septal Defect",
          "AV septal defect",
          "AVCD",
          "AVSD",
          "ECD",
          "atrioventricular canal defect",
          "atrioventricular septal defect",
          "common AV canal",
          "common atrioventricular canal",
          "endocardial cushion defect"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A spectrum of septal defects involving the atrial septum; ventricular septum; and the atrioventricular valves (tricuspid valve; bicuspid valve). These defects are due to incomplete growth and fusion of the endocardial cushions which are important in the formation of two atrioventricular canals, site of future atrioventricular valves."
      },
      "child_count": 12,
      "reference_id": "MONDO:0020290"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2732,
      "label": "congenital heart defects, multiple types"
    },
    {
      "id": 19775,
      "label": "familial atrioventricular septal defect"
    }
  ]
}