{
    "disease_id": "DOID:0060980",
    "recommended_name": {
        "id": "DOID:0060980",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060980",
        "name": "polycystic liver disease 1",
        "description": "A polycystic disease characterized by the presence of multiple liver cysts of biliary epithelial origin that has_material_basis_in heterozygous mutation in the PRKCSH gene on chromosome 19p13."
    },
    "synonyms": [
        {
            "id": "MONDO:0008265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008265",
            "name": "polycystic liver disease 1",
            "description": "A polycystic liver disease in which the cause of the disease is a mutation in the PRKCSH gene, and is characterized by the appearance of numerous cysts spread throughout the liver."
        },
        {
            "id": "MONDO:0008265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008265",
            "name": "isolated congenital polycystic liver disease",
            "description": ""
        },
        {
            "id": "MONDO:0008265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008265",
            "name": "isolated polycystic liver disease",
            "description": ""
        },
        {
            "id": "MONDO:0008265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008265",
            "name": "PCLD1",
            "description": ""
        },
        {
            "id": "MONDO:0008265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008265",
            "name": "nonsyndromic congenital polycystic liver disease",
            "description": ""
        },
        {
            "id": "MONDO:0008265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008265",
            "name": "nonsyndromic polycystic liver disease (disease)",
            "description": ""
        },
        {
            "id": "MONDO:0008265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008265",
            "name": "polycystic liver disease 1",
            "description": ""
        },
        {
            "id": "MONDO:0008265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008265",
            "name": "polycystic liver disease 1 with or without kidney cysts",
            "description": ""
        },
        {
            "id": "MONDO:0008265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008265",
            "name": "ADPCLD",
            "description": ""
        },
        {
            "id": "MONDO:0008265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008265",
            "name": "PCLD",
            "description": ""
        },
        {
            "id": "MONDO:0008265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008265",
            "name": "isolated autosomal dominant polycystic liver disease",
            "description": ""
        },
        {
            "id": "MONDO:0008265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008265",
            "name": "polycystic liver disease",
            "description": ""
        },
        {
            "id": "MIM:174050",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/174050",
            "name": "Polycystic liver disease 1 with or without kidney cysts",
            "description": "Polycystic liver disease 1 with or without kidney cysts"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060980"
    ],
    "unlinked_id_list": []
}