Term Name:	spinocerebellar ataxia type 34
Synonyms:
Definition:	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.
Ontology:	Human Disease [DOID:0050981]   ( DOID:0050981 )