{
    "disease_id": "DOID:0111615", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014934", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014934", 
            "name": "spinocerebellar ataxia, autosomal recessive 24"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014934", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014934", 
            "name": "UBA5 autosomal dominant cerebellar ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014934", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014934", 
            "name": "spinocerebellar ataxia, autosomal recessive 24; SCAR24"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014934", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014934", 
            "name": "SCAR24"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014934", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014934", 
            "name": "spinocerebellar ataxia, autosomal recessive type 24"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014934", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014934", 
            "name": "autosomal dominant cerebellar ataxia caused by mutation in UBA5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111615", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111615", 
            "name": "SCAR24"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111615", 
        "description": "An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in UBA5 on chromosome 3q22.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111615", 
        "name": "autosomal recessive spinocerebellar ataxia 24"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111615#disease-associations", 
            "id": "0111615", 
            "database": "Alliance of Genome Resources"
        }
    ]
}