Human genes for spinocerebellar ataxia type 25
Spinocerebellar ataxia type 25 [DOID:0050974]
An autosomal dominant cerebellar ataxia that is characterized by ataxia and sensory neuropathy, has_material_basis_in repeat CAG expansion on chromosome 2p15-p21.
Synonyms: spinocerebellar ataxia type 25, DOID:0050974