{
    "disease_id": "DOID:0050957", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010847", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010847", 
            "name": "spinocerebellar ataxia autosomal dominant with sensory axonal neuropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010847", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010847", 
            "name": "spinocerebellar ataxia 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010847", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010847", 
            "name": "spinocerebellar ataxia 4; SCA4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010847", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010847", 
            "name": "SCA4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010847", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010847", 
            "name": "spinocerebellar ataxia, autosomal dominant, with sensory axonal neuropathy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050957", 
        "description": "An autosomal dominant cerebellar ataxia that is characterized by progresive ataxia, dysarthria and peripheral neuropathy, has_material_basis_in mutation in the SCA4 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050957", 
        "name": "spinocerebellar ataxia type 4"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050957#disease-associations", 
            "id": "0050957", 
            "database": "Alliance of Genome Resources"
        }
    ]
}