{
    "disease_id": "DOID:0111613", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014846", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014846", 
            "name": "autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome due to TUD deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014846", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014846", 
            "name": "spinocerebellar ataxia, autosomal recessive type 23"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014846", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014846", 
            "name": "SCAR23"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014846", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014846", 
            "name": "spinocerebellar ataxia autosomal recessive type 23"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014846", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014846", 
            "name": "spinocerebellar ataxia, autosomal recessive 23; SCAR23"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014846", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014846", 
            "name": "spinocerebellar ataxia, autosomal recessive 23"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111613", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111613", 
            "name": "SCAR23"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111613", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111613", 
            "name": "autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111613", 
        "description": "An autosomal recessive cerebellar ataxia characterized by epilepsy, intellectual disability, and gait ataxia that has_material_basis_in homozygous or compound heterozygous mutation in TDP2 on chromosome 6p22.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111613", 
        "name": "autosomal recessive spinocerebellar ataxia 23"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111613#disease-associations", 
            "id": "0111613", 
            "database": "Alliance of Genome Resources"
        }
    ]
}