{
    "disease_id": "DOID:0060977",
    "recommended_name": {
        "id": "DOID:0060977",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060977",
        "name": "polycystic liver disease 4",
        "description": "A liver disease characterized by adult-onset of liver cysts arising from the bile duct epithelium that has_material_basis_in heterozygous mutation in the LRP5 gene on chromosome 11q13."
    },
    "synonyms": [
        {
            "id": "MONDO:0044327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044327",
            "name": "polycystic liver disease 4 with or without kidney cysts",
            "description": "An autosomal dominant disease characterized by adult-onset of liver cysts arising from the bile duct epithelium, caused by heterozygous mutation in the LRP5 gene. Some patients may develop a few kidney cysts, but these are often incidental and do not result in renal failure."
        },
        {
            "id": "MONDO:0044327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044327",
            "name": "polycystic liver disease 4 with or without kidney cysts",
            "description": ""
        },
        {
            "id": "MONDO:0044327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044327",
            "name": "PCLD4",
            "description": ""
        },
        {
            "id": "MIM:617875",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617875",
            "name": "Polycystic liver disease 4 with or without kidney cysts",
            "description": "Polycystic liver disease 4 with or without kidney cysts"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060977"
    ],
    "unlinked_id_list": []
}