Spinocerebellar Ataxia Type 13

Preferred Label : Spinocerebellar Ataxia Type 13;

NCIt synonyms : SCA13;

NCIt definition : An autosomal dominant form of spinocerebellar ataxia caused by mutation(s) in the KCNC3 gene, encoding voltage-gated potassium channel KCNC3.;

Détails

Origin ID

C214865;

Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
disease_has_primary_anatomic_site
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]

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