Human genes for spinocerebellar ataxia type 38
Spinocerebellar ataxia type 38 [DOID:0050985]
An autosomal dominant cerebellar ataxia that is characterized by slowly progressive ataxia and nystagmus, presenting in mid-adulthood, and has_material_basis_in mutation to the ELOVL5 gene.
Synonyms: spinocerebellar ataxia type 38, DOID:0050985