Human genes for spinocerebellar ataxia type 18
Spinocerebellar ataxia type 18 [DOID:0050969]
An autosomal dominant cerebellar ataxia that is characterized by cerebellar ataxia and sensory neuropathy, has_material_basis_in mutation on chromosome 7q22-q23.
Synonyms: spinocerebellar ataxia type 18, DOID:0050969