Human genes for spinocerebellar ataxia type 2
Spinocerebellar ataxia type 2 [DOID:0050955]
An autosomal dominant cerebellar ataxia that is characterized by ataxia, bulbar palsy, peripheral neuropathy chorea and muscle atrophy, has_material_basis_in mutation in the ATXN2 gene.
Synonyms: spinocerebellar ataxia type 2, DOID:0050955