{
    "disease_id": "DOID:0110858",
    "recommended_name": {
        "id": "DOID:0110858",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110858",
        "name": "polycystic kidney disease 1",
        "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
    },
    "synonyms": [
        {
            "id": "DOID:0110858",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110858",
            "name": "Polycystic Kidney Disease, Adult, Type I",
            "description": ""
        },
        {
            "id": "DOID:0110858",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110858",
            "name": "APKD1",
            "description": ""
        },
        {
            "id": "DOID:0110858",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110858",
            "name": "PKD1",
            "description": ""
        },
        {
            "id": "MONDO:0008263",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008263",
            "name": "polycystic kidney disease 1",
            "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
        },
        {
            "id": "MONDO:0008263",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008263",
            "name": "APKD1",
            "description": ""
        },
        {
            "id": "MONDO:0008263",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008263",
            "name": "PKD1",
            "description": ""
        },
        {
            "id": "MONDO:0008263",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008263",
            "name": "PKD1 autosomal dominant polycystic kidney disease",
            "description": ""
        },
        {
            "id": "MONDO:0008263",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008263",
            "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
            "description": ""
        },
        {
            "id": "MONDO:0008263",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008263",
            "name": "polycystic kidney disease 1",
            "description": ""
        },
        {
            "id": "MONDO:0008263",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008263",
            "name": "polycystic kidney disease type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008263",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008263",
            "name": "Potter type 3 polycystic kidney disease",
            "description": ""
        },
        {
            "id": "MIM:173900",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/173900",
            "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
            "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110858"
    ],
    "unlinked_id_list": []
}