{
    "disease_id": "DOID:0080061", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008943", 
            "name": "CPDIII"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008943", 
            "name": "cerebellar granular cell hypoplasia and mental retardation, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008943", 
            "name": "autosomal recessive spinocerebellar ataxia type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008943", 
            "name": "PMPCA autosomal recessive congenital cerebellar ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008943", 
            "name": "CPD3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008943", 
            "name": "cerebellar hypoplasia, nonprogressive Norman type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008943", 
            "name": "autosomal recessive congenital cerebellar ataxia caused by mutation in PMPCA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008943", 
            "name": "autosomal recessive cerebelloparenchymal disorder type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008943", 
            "name": "cerebelloparenchymal disorder 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008943", 
            "name": "SCAR2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008943", 
            "name": "spinocerebellar ataxia, autosomal recessive 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008943", 
            "name": "CPD 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008943", 
            "name": "spinocerebellar ataxia, autosomal recessive 2; SCAR2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080061", 
        "description": "An autosomal recessive cerebellar ataxia that is characterized by juvenile onset of progressive cerebellar ataxia, axonal sensorimotor peripheral neuropathy, and increased serum alpha-fetoprotein, and has_material_basis_in homozygous or compound heterozygous mutation in the senataxin gene on chromosome 9q34.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080061", 
        "name": "autosomal recessive spinocerebellar ataxia 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080061#disease-associations", 
            "id": "0080061", 
            "database": "Alliance of Genome Resources"
        }
    ]
}