spinocerebellar ataxia type 14

Term ID

DOID:0050964

Synonyms

Definition

An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, dysarthria and dysphagia, has_material_basis_in mutation in the PRKCG gene. https://rarediseases.info.nih.gov/diseases/9867/spinocerebellar-ataxia-14

References

• OMIM:605361

Ontology

Human Disease   ( DOID:0050964 )