Search Ontology:
Human Disease

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
Ontology
Human Disease   ( DOID:0050964 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models