{
    "disease_id": "DOID:0111618", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012549", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012549", 
            "name": "autosomal recessive ataxia, Beauce type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012549", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012549", 
            "name": "spinocerebellar ataxia, autosomal recessive 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012549", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012549", 
            "name": "cerebellar ataxia, autosomal recessive, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012549", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012549", 
            "name": "SCAR8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012549", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012549", 
            "name": "ataxia, recessive, of Beauce"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012549", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012549", 
            "name": "SYNE1-related autosomal recessive cerebellar ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012549", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012549", 
            "name": "autosomal recessive cerebellar ataxia type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012549", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012549", 
            "name": "ARCA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012549", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012549", 
            "name": "spinocerebellar ataxia, autosomal recessive 8; SCAR8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012549", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012549", 
            "name": "spinocerebellar ataxia, autosomal recessive type 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012549", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012549", 
            "name": "spinocerebellar ataxia autosomal recessive 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012549", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012549", 
            "name": "autosomal recessive ataxia Beauce type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012549", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012549", 
            "name": "recessive ataxia of Beauce"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111618", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111618", 
            "name": "ARCA1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111618", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111618", 
            "name": "Autosomal recessive cerebellar ataxia type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111618", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111618", 
            "name": "SCAR8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111618", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111618", 
            "name": "autosomal recessive ataxia, Beauce type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111618", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111618", 
            "name": "SYNE1-related autosomal recessive cerebellar ataxia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111618", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111618", 
            "name": "recessive ataxia of Beauce"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111618", 
        "description": "An autosomal recessive cerebellar ataxia characterized by slowly progressive neurodegeneration resulting in gait ataxia and other cerebellar signs, spasticity, secondary musculoskeletal abnormalities, and ocular movement anomalies that has_material_basis_in homozygous or compound heterozygous mutation in SYNE1 on chromosome 6q25.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111618", 
        "name": "autosomal recessive spinocerebellar ataxia 8"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111618#disease-associations", 
            "id": "0111618", 
            "database": "Alliance of Genome Resources"
        }
    ]
}