"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."^^ . . "autosomal recessive spinocerebellar ataxia 23"^^ . "autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency"@en . "OMIM:616949"^^ . "DOID:0111613"^^ . . "disease_ontology"^^ . "ORDO:404493"^^ . . "SCAR23"@en .