Human genes for spinocerebellar ataxia type 8
Spinocerebellar ataxia type 8 [DOID:0050959]
An autosomal dominant cerebellar ataxia that is characterized by slowly progressive dysarthria, bradykinesia, nystagmus and loss of coordination, has_material_basis_in mutation in the ATXN80S gene.
Synonyms: spinocerebellar ataxia type 8, DOID:0050959