{
    "disease_id": "DOID:0050984", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014410", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014410", 
            "name": "spinocerebellar ataxia 37; SCA37"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014410", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014410", 
            "name": "SCA37"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014410", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014410", 
            "name": "spinocerebellar ataxia 37"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014410", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014410", 
            "name": "spinocerebellar ataxia with altered vertical eye movements"
        }, 
        {
            "url": "https://www.omim.org/entry/615945", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:615945", 
            "name": "Spinocerebellar ataxia 37"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050984", 
        "description": "An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia and dysarthria, presenting in mid-adulthood, and has_material_basis_in mutation to the DAB1 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050984", 
        "name": "spinocerebellar ataxia type 37"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615945", 
            "id": "615945", 
            "database": "MIM"
        }
    ]
}