{
  "id": 16706,
  "label": "congenital aortopulmonary window",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016077",
  "properties": {
    "xrefs": [
      "GARD:0000738",
      "MEDGEN:419119",
      "MESH:C537782",
      "Orphanet:2037",
      "UMLS:C2931610",
      "icd11.foundation:1988278118"
    ],
    "synonyms": [
      "congenital aortopulmonary artery fistula",
      "congenital aortopulmonary septal defect",
      "aorta-pulmonary artery fistula",
      "aorto-pulmonary artery fistula",
      "aortopulmonary fistula"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17072,
      "label": "conotruncal heart malformations",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19327
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0008189",
          "ICD9:747.11",
          "MEDGEN:341803",
          "NANDO:2200275",
          "OMIM:217095",
          "Orphanet:2445",
          "SCTID:218728005",
          "UMLS:C1857586"
        ],
        "synonyms": [
          "Taussig-Bing syndrome or defect",
          "conotruncal heart malformations",
          "conotruncal heart malformations, variable",
          "CTHM",
          "Double-outlet right ventricle",
          "conotruncal anomaly face syndrome",
          "conotruncal cardiac defects",
          "interrupted aortic Arch",
          "persistent truncus arteriosus",
          "truncus arteriosus communis"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Conotruncal heart malformations are a group of congenital cardiac outflow tract anomalies that include such defects as tetralogy of Fallot, pulmonary atresia with ventricular septal defect, double-outlet right ventricle (DORV), double-outlet left ventricle, truncus arteriosus and transposition of the great arteries (TGA), among others. This group of defects is frequently found in patients with 22q11.2 deletion syndrome. A deletion of chromosome 22q11.2 has equally been associated in a subset of patients with various types of isolated non-syndromic conotruncal heart malformations (with the exception of DORV and TGA where this is very uncommon)."
      },
      "child_count": 8,
      "reference_id": "MONDO:0016581"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17072,
      "label": "conotruncal heart malformations"
    }
  ]
}