{
    "disease_id": "DOID:0050986", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014475", 
            "name": "SCA40"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014475", 
            "name": "spinocerebellar ataxia 40"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014475", 
            "name": "spinocerebellar ataxia 40; SCA40"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050986", 
        "description": "An autosomal dominant cerebellar ataxia that is characterized by progressive gait abnormalutes, dysarthria, tremor and hyporeflexia, has_material_basis_in muation in the CCDC88C gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050986", 
        "name": "spinocerebellar ataxia type 40"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050986#disease-associations", 
            "id": "0050986", 
            "database": "Alliance of Genome Resources"
        }
    ]
}