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Metadata
ID	DOID:0050962
Name	spinocerebellar ataxia type 12
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
Xrefs	MIM:604326
Parent Relationships	is_a autosomal dominant cerebellar ataxia