{
  "id": 12643,
  "label": "heterotaxy, visceral, 2, autosomal",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011546",
  "properties": {
    "xrefs": [
      "DOID:0051017",
      "GARD:0024805",
      "MEDGEN:237904",
      "OMIM:605376",
      "UMLS:C1415817"
    ],
    "synonyms": [
      "DTGA2",
      "heterotaxy, visceral, 2, autosomal",
      "transposition of the great arteries, dextro-looped 2",
      "HTX2",
      "Htx"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2746,
      "label": "transposition of the great arteries",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19327
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0007795",
          "MEDGEN:21245",
          "MESH:D014188",
          "NANDO:2200258",
          "NCIT:C84742",
          "Orphanet:216675",
          "UMLS:C0040761",
          "icd11.foundation:429190257"
        ],
        "synonyms": [
          "TGA",
          "TGV",
          "complete transposition",
          "great vessels transposition",
          "transposition of great vessels",
          "transposition of the great vessels"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A congenital cardiac defect in which two heart vessels are reversed (transposed)."
      },
      "child_count": 3,
      "reference_id": "MONDO:0000153"
    },
    {
      "id": 18668,
      "label": "visceral heterotaxy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        5714,
        19327
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050545",
          "GARD:0010875",
          "MEDGEN:465273",
          "MedDRA:10059119",
          "MedDRA:10067265",
          "NCIT:C117273",
          "OMIMPS:306955",
          "Orphanet:157769",
          "Orphanet:450",
          "SCTID:14821001",
          "UMLS:C3178805",
          "icd11.foundation:780273165"
        ],
        "synonyms": [
          "heterotaxia",
          "heterotaxia syndrome",
          "heterotaxy syndrome",
          "heterotaxy, visceral",
          "incomplete situs inversus",
          "lateralization defect",
          "partial situs inversus",
          "situs ambiguous",
          "situs ambiguus",
          "visceral heterotaxy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A rare, genetic disorder in which symptoms are generally secondary to the abnormal location of the organs within the thoracic, abdominal, or peritoneal cavities. Anatomic and functional problems can include cardiac defects, intestinal malrotation leading to volvulus, biliary atresia, and various defects of the central nervous system, urinary tract, and skeleton."
      },
      "child_count": 57,
      "reference_id": "MONDO:0018677"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2746,
      "label": "transposition of the great arteries"
    },
    {
      "id": 18668,
      "label": "visceral heterotaxy"
    }
  ]
}