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Metadata
ID	DOID:0050973
Name	spinocerebellar ataxia type 23
Definition	An autosomal dominnant cerebellar ataxia that is characterized by slowly progressive ataxia, dysarthria, slow saccades and hyperreflexia, has_material_basis_in mutation in the PDYN gene. https://rarediseases.info.nih.gov/diseases/9950/spinocerebellar-ataxia-23
Xrefs	OMIM:610245
Parent Relationships	is_a autosomal dominant cerebellar ataxia