{
  "id": 2732,
  "label": "congenital heart defects, multiple types",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0000119",
  "properties": {
    "synonyms": [
      "CHTD"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 8,
  "parents": [
    {
      "id": 7116,
      "label": "congenital heart disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6967,
        21294
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1682",
          "EFO:0005207",
          "ICD9:746.84",
          "ICD9:746.89",
          "ICD9:746.9",
          "MEDGEN:57501",
          "MESH:D006330",
          "NCIT:C95834",
          "SCTID:13213009",
          "UMLS:C0152021",
          "icd11.foundation:2004408087"
        ],
        "synonyms": [
          "heart malformation",
          "congenital anomaly of heart",
          "congenital heart defect",
          "congenital heart defects",
          "Abnormality, heart",
          "abnormalities, heart",
          "defect, congenital heart",
          "defects, congenital heart",
          "heart abnormalities",
          "heart abnormality",
          "heart defect, congenital",
          "heart, malformation Of"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A heart disease that is present at birth. Representative examples include atrial septal defect, ventricular septal defect, tetralogy of Fallot, and patent foramen ovale."
      },
      "child_count": 46,
      "reference_id": "MONDO:0005453"
    }
  ],
  "children": [
    {
      "id": 14494,
      "label": "congenital heart defects, multiple types, 6",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2732,
        19269
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060772",
          "GARD:0024928",
          "MEDGEN:462571",
          "OMIM:613854",
          "UMLS:C3151221"
        ],
        "synonyms": [
          "DTGA3",
          "GDF1 dextro-looped transposition of the great arteries",
          "congenital heart defects, multiple types, 6",
          "dextro-looped transposition of the great arteries caused by mutation in GDF1",
          "dextro-looped transposition of the great arteries type 3",
          "transposition of the great arteries, dextro-looped type 3",
          "CHTD6",
          "transposition of the great arteries, dextro-looped 3",
          "transposition of the great arteries, dextro-looped 3, formerly"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any dextro-looped transposition of the great arteries in which the cause of the disease is a mutation in the GDF1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013463"
    },
    {
      "id": 14998,
      "label": "congenital heart defects, multiple types, 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2732,
        24272
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:767108",
          "OMIM:614954",
          "UMLS:C3554194"
        ],
        "synonyms": [
          "CHTD3",
          "congenital heart defects, multiple types, 3",
          "congenital heart defects, multiple types, with Cardiac rhythm and conduction disturbances"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0013988"
    },
    {
      "id": 15010,
      "label": "congenital heart defects, multiple types, 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2732,
        19327,
        24272
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0024964",
          "MEDGEN:767193",
          "OMIM:614980",
          "UMLS:C3554279"
        ],
        "synonyms": [
          "TAB2 congenital heart malformation",
          "TAB2-related syndromic congenital heart disease",
          "congenital heart defects, multiple types, 2",
          "congenital heart malformation caused by mutation in TAB2",
          "CHTD2"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any congenital heart disease characterized by variable features including polyvalvular heart disease, growth failure, joint hypermobility, hypotonia, and hearing loss due to a variation in the TAB2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014000"
    },
    {
      "id": 15346,
      "label": "congenital heart defects, multiple types, 4",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2732,
        19775
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014344"
    },
    {
      "id": 23722,
      "label": "congenital heart defects, multiple types, 5",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2732,
        24266,
        24272
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1636547",
          "OMIM:617912",
          "UMLS:C4693563"
        ],
        "synonyms": [
          "CHTD5",
          "CONGENITAL heart defects, multiple types, 5"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0060663"
    },
    {
      "id": 25030,
      "label": "MYH-6 related congenital heart defects",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2732,
        24272
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "MYH6 related congenital heart defects"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A heart disease that is present at birth that is caused by a variation in MYH-6. Representative examples include atrial septal defect, ventricular septal defect, tetralogy of Fallot and hypoplastic left heart syndrome."
      },
      "child_count": 0,
      "reference_id": "MONDO:0800442"
    },
    {
      "id": 25356,
      "label": "congenital heart defects, multiple types, 8, with or without heterotaxy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2732,
        24272
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1794252",
          "OMIM:619657",
          "UMLS:C5562042"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0859213"
    },
    {
      "id": 25532,
      "label": "congenital heart defects, multiple types, 9",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2732,
        24272
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1841003",
          "OMIM:620294",
          "UMLS:C5830367"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0859532"
    }
  ],
  "roots": [
    {
      "id": 7116,
      "label": "congenital heart disease"
    }
  ]
}