DISEASES

Disease-gene associations mined from literature

Human genes for spinocerebellar ataxia type 14

Spinocerebellar ataxia type 14 [DOID:0050964]

An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, dysarthria and dysphagia, has_material_basis_in mutation in the PRKCG gene.

Synonyms:  spinocerebellar ataxia type 14,  DOID:0050964