{
    "disease_id": "DOID:0050955", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008458", 
            "name": "spinocerebellar ataxia Cuban type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008458", 
            "name": "amyotrophic lateral sclerosis 13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008458", 
            "name": "spinocerebellar atrophy 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008458", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008458", 
            "name": "spinocerebellar ataxia with slow eye movements"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008458", 
            "name": "olivopontocerebellar atrophy, Holguin type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008458", 
            "name": "spinocerebellar ataxia 2; SCA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008458", 
            "name": "amyotrophic lateral sclerosis, susceptibility to, 13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008458", 
            "name": "Wadia-swami syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008458", 
            "name": "spinocerebellar Degeneration with slow eye movements"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008458", 
            "name": "ATXN2 autosomal dominant cerebellar ataxia type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008458", 
            "name": "amyotrophic lateral sclerosis type 13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008458", 
            "name": "olivopontocerebellar atrophy 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008458", 
            "name": "ALS13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008458", 
            "name": "cerebellar Degeneration with slow eye movements"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008458", 
            "name": "OPCA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008458", 
            "name": "Wadia swami syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008458", 
            "name": "autosomal dominant cerebellar ataxia type I caused by mutation in ATXN2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008458", 
            "name": "spinocerebellar ataxia, Cuban type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008458", 
            "name": "olivopontocerebellar atrophy Holguin type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008458", 
            "name": "SCA 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008458", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008458", 
            "name": "SCA2"
        }, 
        {
            "url": "https://www.omim.org/entry/183090", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:183090", 
            "name": "Spinocerebellar ataxia 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050955", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050955", 
        "name": "spinocerebellar ataxia type 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/183090", 
            "id": "183090", 
            "database": "MIM"
        }
    ]
}