{
    "disease_id": "DOID:0050973", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012449", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012449", 
            "name": "spinocerebellar ataxia 23; SCA23"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012449", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012449", 
            "name": "spinocerebellar ataxia 23"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012449", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012449", 
            "name": "SCA23"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050973", 
        "description": "An autosomal dominnant cerebellar ataxia that is characterized by slowly progressive ataxia, dysarthria, slow saccades and hyperreflexia, has_material_basis_in mutation in the PDYN gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050973", 
        "name": "spinocerebellar ataxia type 23"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050973#disease-associations", 
            "id": "0050973", 
            "database": "Alliance of Genome Resources"
        }
    ]
}