{
  "id": 9570,
  "label": "polycystic kidney disease 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008263",
  "properties": {
    "xrefs": [
      "DOID:0110858",
      "GARD:0018597",
      "MEDGEN:461191",
      "MESH:C536326",
      "OMIM:173900",
      "SCTID:253878003",
      "UMLS:C3149841"
    ],
    "synonyms": [
      "APKD1",
      "PKD1",
      "PKD1 autosomal dominant polycystic kidney disease",
      "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
      "polycystic kidney disease 1",
      "polycystic kidney disease type 1",
      "Potter type 3 polycystic kidney disease",
      "Potter type 3 polycystic kidney disease, formerly",
      "polycystic kidney disease 1 with or without polycystic liver disease",
      "polycystic kidney disease, adult",
      "polycystic kidney disease, adult, type 1"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ],
    "definition": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 6472,
      "label": "autosomal dominant polycystic kidney disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        20057
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:898",
          "EFO:1001496",
          "ICD9:753.12",
          "ICD9:753.13",
          "MEDGEN:88404",
          "MESH:D016891",
          "NANDO:1200368",
          "NANDO:2200153",
          "NCIT:C84578",
          "NORD:828",
          "Orphanet:730",
          "SCTID:765330003",
          "UMLS:C0085413",
          "icd11.foundation:91220434"
        ],
        "synonyms": [
          "ADPKD",
          "autosomal dominant polycystic kidney disease",
          "polycystic kidney disease, autosomal dominant",
          "congenital biliary ectasias"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "Autosomal dominant form of polycystic kidney disease."
      },
      "child_count": 14,
      "reference_id": "MONDO:0004691"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6472,
      "label": "autosomal dominant polycystic kidney disease"
    }
  ]
}