Human genes for spinocerebellar ataxia type 1
Spinocerebellar ataxia type 1 [DOID:0050954]
An autosomal dominant cerebellar ataxia that is characterized by ataxia, dysarthria, dysphagia, dystonia and peripheral neuropathy that begins in early adulthood, has_material_basis_in the expanded (CAG)n trinucleotide repeat of ataxin-1 gene on chromosome 6p22.
Synonyms: spinocerebellar ataxia type 1, DOID:0050954