spinocerebellar ataxia type 30

Term ID

DOID:0050979

Synonyms

Definition

An autosomal dominant cerebellar ataxia that is characterized by slowly progressive gait abnormalities and dysarthria, has_material_basis_in mutation in the ODZ3 gene. https://www.omim.org/entry/613371

References

• GARD:4950
• OMIM:613371

Ontology

Human Disease   ( DOID:0050979 )