spinocerebellar ataxia type 12

Term ID

DOID:0050962

Synonyms

Definition

An autosomal dominant cerebellar ataxia that is characterized by minor ataxia and intention tremor, has_material_basis_in CAG expansion of the PPP2R2B gene. https://rarediseases.info.nih.gov/diseases/10476/spinocerebellar-ataxia-12

References

• OMIM:604326

Ontology

Human Disease   ( DOID:0050962 )