Human genes for spinocerebellar ataxia type 34
Spinocerebellar ataxia type 34 [DOID:0050981]
An autosomal dominant cerebellar ataxia that is characterized by papulosquamous, ichthyosiform plaques at birth and progressive ataxia, dysarthria, nystagmus and hyporeflexia, has_material_basis_in mutation in the ELOVL4 gene.
Synonyms: spinocerebellar ataxia type 34, DOID:0050981