{
    "disease_id": "DOID:0111744", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014626", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014626", 
            "name": "spinocerebellar ataxia type 41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014626", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014626", 
            "name": "spinocerebellar ataxia 41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014626", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014626", 
            "name": "spinocerebellar ataxia 41; SCA41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014626", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014626", 
            "name": "SCA41"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111744", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111744", 
            "name": "SCA41"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111744", 
        "description": "An autosomal dominant cerebellar ataxia that has_material_basis_in heterozygous mutation in TRPC3 on chromosome 4q27.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111744", 
        "name": "cerebellar ataxia type 41"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111744#disease-associations", 
            "id": "0111744", 
            "database": "Alliance of Genome Resources"
        }
    ]
}