{
    "disease_id": "DOID:0050958",
    "recommended_name": {
        "id": "DOID:0050958",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050958",
        "name": "spinocerebellar ataxia 7",
        "description": "An autosomal dominant cerebellar ataxia that is characterized by ataxia, progressive vision loss, and failure to thrive, has_material_basis_in mutation in the ATXN7 gene."
    },
    "synonyms": [
        {
            "id": "MONDO:0016163",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0016163",
            "name": "spinocerebellar ataxia 7",
            "description": ""
        },
        {
            "id": "MONDO:0016163",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0016163",
            "name": "ADCA2",
            "description": ""
        },
        {
            "id": "MONDO:0016163",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0016163",
            "name": "ADCAII",
            "description": ""
        },
        {
            "id": "MONDO:0016163",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0016163",
            "name": "ATXN7 autosomal dominant cerebellar ataxia type II",
            "description": ""
        },
        {
            "id": "MONDO:0016163",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0016163",
            "name": "SCA7",
            "description": ""
        },
        {
            "id": "MONDO:0016163",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0016163",
            "name": "ataxia with pigmentary retinopathy",
            "description": ""
        },
        {
            "id": "MONDO:0016163",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0016163",
            "name": "autosomal dominant cerebellar ataxia type 2",
            "description": ""
        },
        {
            "id": "MONDO:0016163",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0016163",
            "name": "autosomal dominant cerebellar ataxia type II",
            "description": ""
        },
        {
            "id": "MONDO:0016163",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0016163",
            "name": "autosomal dominant cerebellar ataxia type II caused by mutation in ATXN7",
            "description": ""
        },
        {
            "id": "MONDO:0016163",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0016163",
            "name": "cerebellar syndrome-pigmentary maculopathy syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0016163",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0016163",
            "name": "spinocerebellar ataxia 7",
            "description": ""
        },
        {
            "id": "MONDO:0016163",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0016163",
            "name": "spinocerebellar ataxia type 7",
            "description": ""
        },
        {
            "id": "MONDO:0016163",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0016163",
            "name": "ADCA, type II",
            "description": ""
        },
        {
            "id": "MONDO:0016163",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0016163",
            "name": "OPCA III",
            "description": ""
        },
        {
            "id": "MONDO:0016163",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0016163",
            "name": "OPCA3",
            "description": ""
        },
        {
            "id": "MIM:164500",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/164500",
            "name": "Spinocerebellar ataxia 7",
            "description": "Spinocerebellar ataxia 7"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050958"
    ],
    "unlinked_id_list": []
}