{
  "id": 23610,
  "label": "polycystic liver disease 3 with or without kidney cysts",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0054743",
  "properties": {
    "xrefs": [
      "DOID:0060976",
      "GARD:0025967",
      "MEDGEN:1646969",
      "OMIM:617874",
      "UMLS:C4693472"
    ],
    "synonyms": [
      "polycystic liver disease 3 with or without kidney cysts",
      "PCLD3"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Any polycystic kidney disease in which the cause of the disease is a mutation in the ALG8 gene, that presents with or without kidney cysts."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2911,
      "label": "autosomal dominant polycystic liver disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        6878
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050770",
          "GARD:0009457",
          "HP:0006557",
          "ICD10CM:Q44.6",
          "ICD9:751.62",
          "MEDGEN:56388",
          "MedDRA:10010427",
          "MedDRA:10048834",
          "MedDRA:10083939",
          "NCIT:C82833",
          "OMIMPS:174050",
          "Orphanet:2924",
          "SCTID:72925005",
          "UMLS:C0158683",
          "icd11.foundation:1361740083",
          "icd11.foundation:423904268"
        ],
        "synonyms": [
          "AD polycystic liver disease",
          "ADPLD",
          "PCLD",
          "isolated congenital polycystic liver disease",
          "isolated polycystic liver disease",
          "polycystic liver disease",
          "congenital cystic liver disease",
          "congenital hepatic cyst",
          "fibrocystic liver disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "An autosomal dominant inherited condition characterized by many cysts of various sizes scattered throughout the liver."
      },
      "child_count": 10,
      "reference_id": "MONDO:0000447"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2911,
      "label": "autosomal dominant polycystic liver disease"
    }
  ]
}