spinocerebellar ataxia type 10

Term ID

DOID:0050960

Synonyms

Definition

An autosomal dominant cerebellar ataxia that is characterized by gait ataxia, upper-limb ataxia, dysarthria and dysphagia, has_material_basis_in mutation in the ATXN10 gene. https://www.ncbi.nlm.nih.gov/books/NBK1175/

References

• GARD:10474
• OMIM:603516

Ontology

Human Disease   ( DOID:0050960 )