{
  "id": 9924,
  "label": "VACTERL/vater association",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008642",
  "properties": {
    "xrefs": [
      "DOID:14679",
      "GARD:0005443",
      "ICD9:759.89",
      "MEDGEN:902479",
      "MedDRA:10053665",
      "MedDRA:10066022",
      "NANDO:1200657",
      "NANDO:2200983",
      "NCIT:C99105",
      "NORD:1818",
      "OMIM:192350",
      "Orphanet:887",
      "SCTID:27742002",
      "UMLS:C4225671",
      "icd11.foundation:1452617987"
    ],
    "synonyms": [
      "VACTERL Association",
      "VACTERL association",
      "VATER association",
      "vertebral abnormalities, anal atresia, Cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects syndrome",
      "VATER/VACTERL association"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "VACTERL/VATER is an association of congenital malformations typically characterized by the presence of at least three of the following: vertebral defects, anal atresia, cardiac defects, tracheo-esophageal fistula, renal anomalies, and limb abnormalities."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    }
  ],
  "children": [
    {
      "id": 11892,
      "label": "VACTERL association, X-linked, with or without hydrocephalus",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        5714,
        9924,
        11354
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111766",
          "GARD:0015309",
          "MEDGEN:419019",
          "OMIM:314390",
          "UMLS:C2931228"
        ],
        "synonyms": [
          "VACTERL association, X-linked, X-linked recessive",
          "VACTERL association, X-linked, with or without hydrocephalus",
          "VACTERL association with hydrocephaly, X-linked",
          "VACTERL-H, X-linked",
          "VACTERLX",
          "X-linked VACTERL-H syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010752"
    }
  ],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    }
  ]
}