{
    "disease_id": "DOID:0050976", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012247", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012247", 
            "name": "spinocerebellar ataxia 27; SCA27"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012247", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012247", 
            "name": "cerebellar ataxia autosomal dominant FGF14-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012247", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012247", 
            "name": "SCA27"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012247", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012247", 
            "name": "spinocerebellar ataxia 27"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012247", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012247", 
            "name": "cerebellar ataxia, autosomal dominant, Fgf14-related"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050976", 
        "description": "An autosomal dominant cerebellar ataxia that is characterized by slowly progressive ataxia, early-onset tremor and dyskinesia, and has_material_basis_in mutation in the FGF14 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050976", 
        "name": "spinocerebellar ataxia type 27"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050976#disease-associations", 
            "id": "0050976", 
            "database": "Alliance of Genome Resources"
        }
    ]
}