spinocerebellar ataxia type 35

Term ID

DOID:0050982

Synonyms

Definition

An autosomal dominant cerebellar ataxia that is characterized by a slowly progressive ataxia, tremor, dysarthria and hyperreflexia, has_material_basis_in mutation in the TGM6 gene. https://www.omim.org/entry/613908

References

• OMIM:613908

Ontology

Human Disease   ( DOID:0050982 )