Human genes for spinocerebellar ataxia type 17
Spinocerebellar ataxia type 17 [DOID:0050967]
An autosomal dominant cerebellar ataxia that is characterized by chorea, dementia, dystonia, spasiticity and seizure, has_material_basis_in CAG repeat expansion in the TBP gene.
Synonyms: spinocerebellar ataxia type 17, DOID:0050967