Human genes for spinocerebellar ataxia type 11
Spinocerebellar ataxia type 11 [DOID:0050961]
An autosomal dominant cerebellar ataxia that is characterized by ataxia, nystagmus, pyramidal abnormalities and peripheral neuropathy, has_material_basis_in mutation in the TTBK2 gene.
Synonyms: spinocerebellar ataxia type 11, DOID:0050961