{
    "disease_id": "DOID:0060976",
    "recommended_name": {
        "id": "DOID:0060976",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060976",
        "name": "polycystic liver disease 3",
        "description": "A liver disease characterized by the development of multiple liver cysts that usually becomes apparent in adulthood that has_material_basis_in heterozygous mutation in the ALG8 gene on chromosome 11q14."
    },
    "synonyms": [
        {
            "id": "MONDO:0054743",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054743",
            "name": "polycystic liver disease 3 with or without kidney cysts",
            "description": "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."
        },
        {
            "id": "MONDO:0054743",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054743",
            "name": "polycystic liver disease 3 with or without kidney cysts",
            "description": ""
        },
        {
            "id": "MONDO:0054743",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054743",
            "name": "PCLD3",
            "description": ""
        },
        {
            "id": "MIM:617874",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617874",
            "name": "Polycystic liver disease 3 with or without kidney cysts",
            "description": "Polycystic liver disease 3 with or without kidney cysts"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060976"
    ],
    "unlinked_id_list": []
}