Human genes for spinocerebellar ataxia type 31
Spinocerebellar ataxia type 31 [DOID:0050980]
An autosomal dominant cerebellar ataxia that is characterized by late-onset ataxia, dysarthria and horizontal nystagmus, has_material_basis_in repeat expansion mutation in the BEAN1 gene.
Synonyms: spinocerebellar ataxia type 31, DOID:0050980