{
  "id": 22595,
  "label": "polycystic kidney disease 4",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0033004",
  "properties": {
    "xrefs": [
      "DOID:0080212",
      "GARD:0006168",
      "MEDGEN:1621793",
      "OMIM:263200",
      "UMLS:C4540575"
    ],
    "synonyms": [
      "polycystic kidney disease 4, with or without hepatic disease",
      "PKD3",
      "PKD3, formerly",
      "PKD4",
      "hepatic fibrosis, congenital",
      "polycystic kidney and hepatic disease 1",
      "polycystic kidney disease 4 with or without hepatic disease",
      "polycystic kidney disease 4 with or without polycystic liver disease",
      "polycystic kidney disease, autosomal recessive",
      "polycystic kidney disease, infantile, type 1"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ],
    "definition": "A autosomal dominant polycystic kidney disease that has material basis in mutation in the PKD4 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 11092,
      "label": "autosomal recessive polycystic kidney disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7611,
        20057
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110861",
          "GARD:0008378",
          "ICD9:753.14",
          "MEDGEN:39076",
          "MedDRA:10036047",
          "NANDO:1200369",
          "NANDO:2200154",
          "NCIT:C84579",
          "NORD:831",
          "Orphanet:731",
          "SCTID:28770003",
          "UMLS:C0085548",
          "icd11.foundation:1424110943"
        ],
        "synonyms": [
          "AR-PKD",
          "ARPKD",
          "autosomal recessive polycystic kidney",
          "polycystic kidney disease, autosomal recessive",
          "polycystic kidney disease, infantile type",
          "polycystic kidney and hepatic disease 1",
          "polycystic kidney disease, infantile, type I",
          "PKHD1"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "An inherited disorder characterized by the development of cysts affecting the collecting ducts. It is frequently associated with hepatic involvement."
      },
      "child_count": 4,
      "reference_id": "MONDO:0009889"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 11092,
      "label": "autosomal recessive polycystic kidney disease"
    }
  ]
}