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Human Disease
spinocerebellar ataxia type 12
- Term ID
- DOID:0050962
- Synonyms
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- 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
- References
- Ontology
- Human Disease ( DOID:0050962 )
- is a type of
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