{
  "id": 23722,
  "label": "congenital heart defects, multiple types, 5",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0060663",
  "properties": {
    "xrefs": [
      "MEDGEN:1636547",
      "OMIM:617912",
      "UMLS:C4693563"
    ],
    "synonyms": [
      "CHTD5",
      "CONGENITAL heart defects, multiple types, 5"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ]
  },
  "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": 24266,
      "label": "GATA5-related congenital heart defects",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7116
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "GATA5 related congenital heart defects"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A congenital heart disease that is present at birth. Representative examples include tetralogy of fallot, bicuspid aortic valve, atrial septal defect, double outlet right ventricle, ventricular septal defect, and coarctation of the aorta, and atrioventricular canal."
      },
      "child_count": 1,
      "reference_id": "MONDO:0100541"
    },
    {
      "id": 24272,
      "label": "cardiogenetic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6967
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "hereditary heart disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions, with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology that are characterized by abnormalities in the cardiovascular system."
      },
      "child_count": 146,
      "reference_id": "MONDO:0100547"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2732,
      "label": "congenital heart defects, multiple types"
    },
    {
      "id": 24266,
      "label": "GATA5-related congenital heart defects"
    },
    {
      "id": 24272,
      "label": "cardiogenetic disease"
    }
  ]
}