Human genes for spinocerebellar ataxia type 23
Spinocerebellar ataxia type 23 [DOID:0050973]
An autosomal dominnant cerebellar ataxia that is characterized by slowly progressive ataxia, dysarthria, slow saccades and hyperreflexia, has_material_basis_in mutation in the PDYN gene.
Synonyms: spinocerebellar ataxia type 23, DOID:0050973