{
  "id": 21763,
  "label": "congenital anomalies of kidney and urinary tract 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0027676",
  "properties": {
    "xrefs": [
      "DOID:0080207",
      "GARD:0025500",
      "MEDGEN:1804316",
      "OMIM:143400",
      "UMLS:C5574705"
    ],
    "synonyms": [
      "TBX18 congenital anomaly of kidney and urinary tract",
      "congenital anomalies of kidney and urinary tract 2",
      "congenital anomalies of kidney and urinary tract type 2",
      "congenital anomaly of kidney and urinary tract caused by mutation in TBX18",
      "CAKUT2",
      "hydronephrosis due to Pujo",
      "multicystic renal dysplasia, bilateral",
      "pelviureteric junction obstruction",
      "ureteropelvic junction obstruction"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ],
    "definition": "Any congenital anomaly of kidney and urinary tract in which the cause of the disease is a mutation in the TBX18 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19481,
      "label": "congenital anomaly of kidney and urinary tract",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19507,
        23932
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080205",
          "GARD:0019216",
          "MEDGEN:369894",
          "MESH:C566906",
          "OMIMPS:610805",
          "Orphanet:93545",
          "UMLS:C1968949"
        ],
        "synonyms": [
          "CAKUT",
          "congenital anomalies of kidney and urinary tract",
          "congenital anomaly of kidney and urinary tract",
          "renal or urinary tract malformation"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "A urinary system disease characterized by structural malformations in the kidney and/or urinary tract containing vesicoureteral reflux."
      },
      "child_count": 6,
      "reference_id": "MONDO:0019719"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19481,
      "label": "congenital anomaly of kidney and urinary tract"
    }
  ]
}