{
    "disease_id": "DOID:0050962", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011439", 
            "name": "SCA12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011439", 
            "name": "spinocerebellar ataxia 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011439", 
            "name": "spinocerebellar ataxia 12; SCA12"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050962", 
        "description": "An autosomal dominant cerebellar ataxia that is characterized by minor ataxia and intention tremor, has_material_basis_in CAG expansion of the PPP2R2B gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050962", 
        "name": "spinocerebellar ataxia type 12"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050962#disease-associations", 
            "id": "0050962", 
            "database": "Alliance of Genome Resources"
        }
    ]
}