DISEASES

Disease-gene associations mined from literature

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 abonormalities and peripheral neuropathy, has_material_basis_in mutation in the TTBK2 gene.

Synonyms:  spinocerebellar ataxia type 11,  DOID:0050961