{
    "disease_id": "DOID:0050978", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007298", 
            "name": "SCA29"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007298", 
            "name": "cerebellar ataxia early-onset nonprogressive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007298", 
            "name": "aplasia of cerebellar vermis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007298", 
            "name": "spinocerebellar ataxia 29; SCA29"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007298", 
            "name": "spinocerebellar ataxia 29"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007298", 
            "name": "cerebellar ataxia, congenital nonprogressive, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007298", 
            "name": "congenital nonprogressive spinocerebellar ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007298", 
            "name": "ACV"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007298", 
            "name": "cerebellar vermis aplasia"
        }, 
        {
            "url": "https://www.omim.org/entry/117360", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:117360", 
            "name": "Spinocerebellar ataxia 29"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050978", 
        "description": "An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, intellectual disability, dysarthria and ophthalmoplegia, and has_material_basis_in mutation in the ITPR1 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050978", 
        "name": "spinocerebellar ataxia type 29"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/117360", 
            "id": "117360", 
            "database": "MIM"
        }
    ]
}