{
    "disease_id": "DOID:1441",
    "recommended_name": {
        "id": "DOID:1441",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:1441",
        "name": "autosomal dominant cerebellar ataxia",
        "description": "A cerebellar ataxia that has_material_basis_in autosomal dominant inheritance."
    },
    "synonyms": [
        {
            "id": "DOID:1441",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:1441",
            "name": "spinocerebellar ataxia",
            "description": ""
        },
        {
            "id": "MONDO:0008119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008119",
            "name": "spinocerebellar ataxia type 1",
            "description": "Spinocerebellar ataxia type 1 (SCA1) is a subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term) characterized by dysarthria, writing difficulties, limb ataxia, and commonly nystagmus and saccadic abnormalities."
        },
        {
            "id": "MONDO:0008119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008119",
            "name": "ATXN1 autosomal dominant cerebellar ataxia type I",
            "description": ""
        },
        {
            "id": "MONDO:0008119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008119",
            "name": "OPCA4",
            "description": ""
        },
        {
            "id": "MONDO:0008119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008119",
            "name": "cerebelloparenchymal disorder 1",
            "description": ""
        },
        {
            "id": "MONDO:0008119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008119",
            "name": "spinocerebellar atrophy 1",
            "description": ""
        },
        {
            "id": "MONDO:0008119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008119",
            "name": "spinocerebellar ataxia 1",
            "description": ""
        },
        {
            "id": "MONDO:0008119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008119",
            "name": "OPCA1",
            "description": ""
        },
        {
            "id": "MONDO:0008119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008119",
            "name": "spinocerebellar ataxia type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008119",
            "name": "autosomal dominant cerebellar ataxia type I caused by mutation in ATXN1",
            "description": ""
        },
        {
            "id": "MONDO:0008119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008119",
            "name": "OPCA 4",
            "description": ""
        },
        {
            "id": "MONDO:0008119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008119",
            "name": "olivopontocerebellar atrophy 4",
            "description": ""
        },
        {
            "id": "MONDO:0008119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008119",
            "name": "spinocerebellar ataxia 1; Sca1",
            "description": ""
        },
        {
            "id": "MONDO:0008119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008119",
            "name": "OPCA 1",
            "description": ""
        },
        {
            "id": "MONDO:0008119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008119",
            "name": "Menzel type OPCA",
            "description": ""
        },
        {
            "id": "MONDO:0008119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008119",
            "name": "olivopontocerebellar atrophy 1",
            "description": ""
        },
        {
            "id": "MONDO:0008119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008119",
            "name": "Schut-haymaker type OPCA",
            "description": ""
        },
        {
            "id": "MONDO:0008119",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008119",
            "name": "Sca1",
            "description": ""
        },
        {
            "id": "MIM:164400",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/164400",
            "name": "Spinocerebellar ataxia 1",
            "description": "Spinocerebellar ataxia 1"
        }
    ]
}