DISEASES

Disease-gene associations mined from literature

Human genes for spinocerebellar ataxia type 26

Spinocerebellar ataxia type 26 [DOID:0050975]

An autosomal dominant cerebellar ataxia that is characterized by slowly progressive ataxia and oculomotor abnormalities, has_material_basis_in mutation in the EEF2 gene.

Synonyms:  spinocerebellar ataxia type 26,  DOID:0050975