{
    "disease_id": "DOID:0080060", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013687", 
            "name": "SCAR12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013687", 
            "name": "WWOX autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013687", 
            "name": "autosomal recessive spinocerebellar ataxia type 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013687", 
            "name": "spinocerebellar ataxia, autosomal recessive 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013687", 
            "name": "autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome due to WWOX deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013687", 
            "name": "WWOX autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013687", 
            "name": "spinocerebellar ataxia, autosomal recessive 12; SCAR12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013687", 
            "name": "autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome caused by mutation in WWOX"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013687", 
            "name": "spinocerebellar ataxia with mental retardation and epilepsy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013687", 
            "name": "autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome caused by mutation in WWOX"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013687", 
            "name": "spinocerebellar ataxia, autosomal recessive type 12"
        }, 
        {
            "url": "https://www.omim.org/entry/614322", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:614322", 
            "name": "Spinocerebellar ataxia, autosomal recessive, 12"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080060", 
        "description": "An autosomal recessive cerebellar ataxia that is characterized by onset of generalized seizures in infancy, delayed psychomotor development with mental retardation, and cerebellar ataxia and that has_material_basis_in homozygous mutation in the WWOX gene on chromosome 16q23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080060", 
        "name": "autosomal recessive spinocerebellar ataxia 12"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614322", 
            "id": "614322", 
            "database": "MIM"
        }
    ]
}