{
    "disease_id": "DOID:0080059", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012235", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012235", 
            "name": "childhood onset autosomal recessive slowly progressive spinocerebellar ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012235", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012235", 
            "name": "SCAR7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012235", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012235", 
            "name": "autosomal recessive spinocerebellar ataxia type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012235", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012235", 
            "name": "childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012235", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012235", 
            "name": "spinocerebellar ataxia, autosomal recessive 7; SCAR7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012235", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012235", 
            "name": "spinocerebellar ataxia, autosomal recessive type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012235", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012235", 
            "name": "spinocerebellar ataxia autosomal recessive 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012235", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012235", 
            "name": "spinocerebellar ataxia, autosomal recessive 7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080059", 
        "description": "An autosomal recessive cerebellar ataxia that is characterized by onset of progressive gait difficulties, eye movement abnormalities, and dysarthria in the first or second decade of life and that has_material_basis_in compound heterozygous mutation in the TPP1 gene on chromosome 11p15.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080059", 
        "name": "autosomal recessive spinocerebellar ataxia 7"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080059#disease-associations", 
            "id": "0080059", 
            "database": "Alliance of Genome Resources"
        }
    ]
}