{
    "disease_id": "DOID:0050980",
    "recommended_name": {
        "id": "DOID:0050980",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0050980",
        "name": "spinocerebellar ataxia type 31",
        "description": "An autosomal dominant cerebellar ataxia that is characterized by late-onset ataxia, dysarthria and horizontal nystagmus, has_material_basis_in repeat expansion mutation in the BEAN1 gene."
    },
    "synonyms": [
        {
            "id": "MONDO:0007296",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007296",
            "name": "spinocerebellar ataxia type 31",
            "description": "Spinocerebellar ataxia type 31 (SCA31) is a very rare subtype of autosomal dominant cerebellar ataxia type III (ADCA type III) characterized by the late-onset of cerebral ataxia, dysarthria and horizontal gaze nystagmus, and that is occasionally accompanied by pyramidal signs, tremor, decreased vibration sense and hearing difficulties."
        },
        {
            "id": "MONDO:0007296",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007296",
            "name": "SCA31",
            "description": ""
        },
        {
            "id": "MONDO:0007296",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007296",
            "name": "spinocerebellar ataxia type 31",
            "description": ""
        },
        {
            "id": "MONDO:0007296",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007296",
            "name": "spinocerebellar ataxia 16q22-linked",
            "description": ""
        },
        {
            "id": "MONDO:0007296",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007296",
            "name": "spinocerebellar ataxia 31",
            "description": ""
        },
        {
            "id": "MONDO:0007296",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007296",
            "name": "spinocerebellar ataxia, 16Q22-linked",
            "description": ""
        },
        {
            "id": "MIM:117210",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/117210",
            "name": "Spinocerebellar ataxia 31",
            "description": "Spinocerebellar ataxia 31"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050980"
    ],
    "unlinked_id_list": []
}