{
  "id": 11223,
  "label": "situs inversus",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010029",
  "properties": {
    "xrefs": [
      "DOID:758",
      "GARD:0004883",
      "HP:0001696",
      "ICD10CM:Q89.3",
      "ICD9:759.3",
      "ICD9:759.89",
      "MEDGEN:1642262",
      "MESH:D012857",
      "NCIT:C87121",
      "Orphanet:101063",
      "SCTID:24614000",
      "UMLS:C4551493",
      "icd11.foundation:797648408"
    ],
    "synonyms": [
      "complete situs inversus",
      "complete situs inversus viscerum",
      "complete transposition (morphologic abnormality)",
      "situs inversus",
      "situs inversus totalis",
      "situs inversus totalis (disease)",
      "situs ambiguus"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "A congenital condition in which there is complete right-to-left reversal of the position of the major thoracic and abdominal organs (that is, they are arranged in a mirror image of the normal positioning)."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "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": [
    {
      "id": 12464,
      "label": "situs inversus totalis with cystic dysplasia of kidneys and pancreas",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        11223
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0008567",
          "MEDGEN:400349",
          "MESH:C536666",
          "OMIM:603643",
          "UMLS:C1863647"
        ],
        "synonyms": [
          "situs inversus totalis with cystic dysplasia of kidneys and pancreas",
          "situs inversus, cystic dysplastic kidney and pancreas, bowed lower limbs,severe intrauterine growth retardation, and oligohydramnios"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0011354"
    }
  ],
  "roots": [
    {
      "id": 18668,
      "label": "visceral heterotaxy"
    }
  ]
}