{
  "id": 19887,
  "label": "congenital Gerbode defect",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020428",
  "properties": {
    "xrefs": [
      "GARD:0019647",
      "MEDGEN:576645",
      "NANDO:2100090",
      "NANDO:2200274",
      "Orphanet:99095",
      "SCTID:204312002",
      "UMLS:C0344947",
      "icd11.foundation:1370033158"
    ],
    "synonyms": [
      "Gerbode defect",
      "left ventricular-to-right atrial communication"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19327,
      "label": "congenital heart malformation",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        21294
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0005269",
          "MEDGEN:1680993",
          "Orphanet:88991",
          "UMLS:C3649636"
        ],
        "synonyms": [
          "congenital heart malformation",
          "disorder of heart development",
          "heart development disease",
          "congenital non-syndromic heart malformation",
          "rare congenital non-syndromic heart malformation"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A disease that has its basis in the disruption of heart development."
      },
      "child_count": 26,
      "reference_id": "MONDO:0019512"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19327,
      "label": "congenital heart malformation"
    }
  ]
}