{
    "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": [],
    "crossref": [
        {
            "id": "DOID:0110858",
            "database": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110858",
            "categories": []
        },
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            "url": "https://monarchinitiative.org/disease/MONDO:0008263",
            "categories": []
        },
        {
            "id": "MIM:173900",
            "database": "MIM",
            "url": "https://www.omim.org/entry/173900",
            "categories": []
        }
    ],
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            "uniprot_ac": "A0A8M9QMX0",
            "uniprot_id": "A0A8M9QMX0_DANRE",
            "refseq_ac": "XP_021335980",
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                }
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                }
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                    "name": "C-Myc1",
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                    "name": "cellular myelocytomatosis oncogene",
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                    "type": "synonym"
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                    "name": "v-myc avian myelocytomatosis viral oncogene homolog a",
                    "type": "synonym"
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                    "name": "myca",
                    "type": "recommended"
                },
                {
                    "name": "MYC",
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                    "id": "0110858",
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                }
            ]
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            "uniprot_ac": "Q7ZVS9",
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                {
                    "name": "C-Myc2",
                    "type": "synonym"
                },
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                    "name": "c-Myc-B",
                    "type": "synonym"
                },
                {
                    "name": "cmycb",
                    "type": "synonym"
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                    "name": "myelocytomatosis oncogene b",
                    "type": "synonym"
                },
                {
                    "name": "transcriptional regulator Myc-B",
                    "type": "synonym"
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                    "name": "v-myc avian myelocytomatosis viral oncogene homolog b",
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                    "name": "mycb",
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                {
                    "name": "mycb",
                    "type": "synonym"
                },
                {
                    "name": "zgc:55680",
                    "type": "synonym"
                }
            ],
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                    "id": "0110858",
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        },
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            "uniprot_canonical_ac": "O08852-1",
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                    "name": "Mus musculus",
                    "taxid": 10090,
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                    "glygen_name": "Mouse",
                    "reference_species": "Mus musculus [10090]"
                }
            ],
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                    "name": "Polycystin-1",
                    "type": "recommended"
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                {
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                    "type": "synonym"
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                {
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                    "type": "synonym"
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                    "name": "polycystin 1, transient receptor poteintial channel interacting",
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                    "name": "polycystin-1 precursor",
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                    "name": "polycystin-1",
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                }
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                {
                    "name": "Pkd1",
                    "type": "recommended"
                },
                {
                    "name": "PC1",
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                },
                {
                    "name": "Pkd1",
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                },
                {
                    "name": "mFLJ00285",
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                    "id": "0110858",
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                    "name": "Mus musculus",
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                    "name": "Myc proto-oncogene protein",
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                    "name": "Proto-oncogene c-Myc",
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                    "name": "myc proto-oncogene protein isoform b",
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                    "name": "myelocytomatosis oncogene",
                    "type": "synonym"
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                    "name": "Niard",
                    "type": "synonym"
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                    "name": "Nird",
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                    "name": "Homo sapiens",
                    "taxid": 9606,
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                    "glygen_name": "Human",
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                    "name": "polycystin-1",
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                    "name": "PKD1",
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                    "name": "Protein diminutive",
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                    "name": "dMyc",
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                    "name": "diminuitive",
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                    "name": "DM",
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                    "name": "Diminutive",
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                    "name": "Dmel\\CG10798",
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                    "name": "Myc",
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                    "name": "anon-WO03040301.171",
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                    "name": "cMyc",
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                    "name": "dMYC",
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                    "name": "dMyc1",
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                    "name": "dm",
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                    "name": "l(1)G0354",
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                    "name": "l(1)G0359",
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    ],
    "glycans": [],
    "biomarkers": [],
    "association_flag": "1000",
    "record_id": "doid.0110858"
}