{
    "disease_id": "DOID:0051081",
    "recommended_name": {
        "id": "DOID:0051081",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0051081",
        "name": "polycystic kidney disease 8",
        "description": "An autosomal dominant polycystic kidney disease that is characterized by enlarged kidneys, arterial hypertension, and kidney failure and that has_material_basis_in heterozygous mutation in the NEK8 gene on chromosome 17q11."
    },
    "synonyms": [
        {
            "id": "MONDO:0971178",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0971178",
            "name": "polycystic kidney disease 8",
            "description": ""
        },
        {
            "id": "MIM:620903",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620903",
            "name": "Polycystic kidney disease 8",
            "description": "Polycystic kidney disease 8"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0051081"
    ],
    "unlinked_id_list": []
}