DISEASES

Disease-gene associations mined from literature

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