{
    "disease_id": "DOID:0050955",
    "recommended_name": {
        "id": "DOID:0050955",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050955",
        "name": "spinocerebellar ataxia 2",
        "description": "An autosomal dominant cerebellar ataxia that is characterized by ataxia, bulbar palsy, peripheral neuropathy chorea and muscle atrophy, has_material_basis_in mutation in the ATXN2 gene."
    },
    "synonyms": [
        {
            "id": "MONDO:0008458",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008458",
            "name": "spinocerebellar ataxia type 2",
            "description": "A subtype of type I autosomal dominant cerebellar ataxia (ADCA type I) characterized by truncal ataxia, dysarthria, slowed saccades and less commonly ophthalmoparesis and chorea."
        },
        {
            "id": "MONDO:0008458",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008458",
            "name": "ATXN2 autosomal dominant cerebellar ataxia type I",
            "description": ""
        },
        {
            "id": "MONDO:0008458",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008458",
            "name": "OPCA2",
            "description": ""
        },
        {
            "id": "MONDO:0008458",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008458",
            "name": "SCA2",
            "description": ""
        },
        {
            "id": "MONDO:0008458",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008458",
            "name": "autosomal dominant cerebellar ataxia type I caused by mutation in ATXN2",
            "description": ""
        },
        {
            "id": "MONDO:0008458",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008458",
            "name": "spinocerebellar ataxia type 2",
            "description": ""
        },
        {
            "id": "MONDO:0008458",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008458",
            "name": "ALS13",
            "description": ""
        },
        {
            "id": "MONDO:0008458",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008458",
            "name": "SCA 2",
            "description": ""
        },
        {
            "id": "MONDO:0008458",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008458",
            "name": "Wadia swami syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008458",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008458",
            "name": "amyotrophic lateral sclerosis 13",
            "description": ""
        },
        {
            "id": "MONDO:0008458",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008458",
            "name": "olivopontocerebellar atrophy Holguin type",
            "description": ""
        },
        {
            "id": "MONDO:0008458",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008458",
            "name": "spinocerebellar ataxia 2",
            "description": ""
        },
        {
            "id": "MONDO:0008458",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008458",
            "name": "spinocerebellar ataxia Cuban type",
            "description": ""
        },
        {
            "id": "MONDO:0008458",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008458",
            "name": "spinocerebellar ataxia with slow eye movements",
            "description": ""
        },
        {
            "id": "MIM:183090",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/183090",
            "name": "Spinocerebellar ataxia 2",
            "description": "Spinocerebellar ataxia 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050955"
    ],
    "unlinked_id_list": []
}