spinocerebellar ataxia type 23

Term ID

DOID:0050973

Synonyms

Definition

An autosomal dominnant cerebellar ataxia that is characterized by slowly progressive ataxia, dysarthria, slow saccades and hyperreflexia, has_material_basis_in mutation in the PDYN gene. https://rarediseases.info.nih.gov/diseases/9950/spinocerebellar-ataxia-23

References

• OMIM:610245

Ontology

Human Disease   ( DOID:0050973 )