{
    "disease_id": "DOID:0110034",
    "recommended_name": {
        "id": "DOID:0110034",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110034",
        "name": "X-linked Alport syndrome",
        "description": "An Alport syndrome that has_material_basis_in mutation in the gene encoding the alpha-5 chain of basement membrane collagen type IV (COL4A5)."
    },
    "synonyms": [
        {
            "id": "DOID:0110034",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110034",
            "name": "nephropathy and deafness, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010520",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010520",
            "name": "X-linked Alport syndrome",
            "description": "X-linked form of Alport syndrome."
        },
        {
            "id": "MONDO:0010520",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010520",
            "name": "Alport syndrome 1, X-linked, X-linked dominant",
            "description": ""
        },
        {
            "id": "MONDO:0010520",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010520",
            "name": "Alport syndrome, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010520",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010520",
            "name": "X-linked Alport syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010520",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010520",
            "name": "nephropathy and deafness, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010520",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010520",
            "name": "ATS",
            "description": ""
        },
        {
            "id": "MONDO:0010520",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010520",
            "name": "congenital hereditary hematuria",
            "description": ""
        },
        {
            "id": "MONDO:0010520",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010520",
            "name": "hemorrhagic familial nephritis",
            "description": ""
        },
        {
            "id": "MONDO:0010520",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010520",
            "name": "hemorrhagic hereditary nephritis",
            "description": ""
        },
        {
            "id": "MIM:301050",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/301050",
            "name": "Alport syndrome 1, X-linked",
            "description": "Alport syndrome 1, X-linked"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110034"
    ],
    "unlinked_id_list": []
}