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Metadata
ID	DOID:0050964
Name	spinocerebellar ataxia 14
Definition	An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, dysarthria and dysphagia, has_material_basis_in mutation in the PRKCG gene. https://rarediseases.info.nih.gov/diseases/9867/spinocerebellar-ataxia-14
Xrefs	MIM:605361
Parent Relationships	is_a autosomal dominant cerebellar ataxia