{
    "disease_id": "DOID:0111614", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014845", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014845", 
            "name": "spinocerebellar ataxia, autosomal recessive 22"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014845", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014845", 
            "name": "autosomal recessive cerebellar ataxia caused by mutation in VWA3B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014845", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014845", 
            "name": "SCAR22"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014845", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014845", 
            "name": "spinocerebellar ataxia, autosomal recessive 22; SCAR22"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014845", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014845", 
            "name": "VWA3B autosomal recessive cerebellar ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014845", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014845", 
            "name": "spinocerebellar ataxia, autosomal recessive type 22"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111614", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111614", 
            "name": "SCAR22"
        }, 
        {
            "url": "https://www.omim.org/entry/616948", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:616948", 
            "name": "Spinocerebellar ataxia, autosomal recessive, 22"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111614", 
        "description": "An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in VWA3B on chromosome 2q11.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111614", 
        "name": "autosomal recessive spinocerebellar ataxia 22"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616948", 
            "id": "616948", 
            "database": "MIM"
        }
    ]
}