{
    "disease_id": "DOID:0050882", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010848", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010848", 
            "name": "spinocerebellar ataxia 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010848", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010848", 
            "name": "spinocerebellar ataxia 5; SCA5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010848", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010848", 
            "name": "SCA5"
        }, 
        {
            "url": "https://www.omim.org/entry/600224", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:600224", 
            "name": "Spinocerebellar ataxia 5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050882", 
        "description": "An autosomal dominant cerebellar ataxia that is characterized by the early-onset of cerebellar signs and eye movement abnormalities with a very slow disease progression, and has_material_basis_in mutation in the SPTBN2 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050882", 
        "name": "spinocerebellar ataxia type 5"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/600224", 
            "id": "600224", 
            "database": "MIM"
        }
    ]
}