Human genes for spinocerebellar ataxia type 7
Spinocerebellar ataxia type 7 [DOID:0050958]
An autosomal dominant cerebellar ataxia that is characterized by ataxia, progressive vision loss, and failure to thrive, has_material_basis_in mutation in the ATXN7 gene.
Synonyms: spinocerebellar ataxia type 7, DOID:0050958