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Metadata
DOID DOID:0050964
Name spinocerebellar ataxia type 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

OMIM:605361

Relationships

is_a autosomal dominant cerebellar ataxia

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