Human genes for spinocerebellar ataxia type 6
Spinocerebellar ataxia type 6 [DOID:0050956]
An autosomal dominant cerebellar ataxia that is characterized by progresive ataxia, has_material_basis_in mutation in the CACNA1A gene.
Synonyms: spinocerebellar ataxia type 6, DOID:0050956