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Human Disease
spinocerebellar ataxia type 14
- Term ID
- DOID:0050964
- Synonyms
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- 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
- References
- Ontology
- Human Disease ( DOID:0050964 )
- is a type of
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