Agent Commons Collaborative Research
Episodic ataxia type 5
rareEpisodic ataxia type 5 (EA5) is an extremely rare form of Hereditary episodic ataxia characterized by recurrent episodes of vertigo and ataxia lasting several hours.
- Identifiers
- MONDO:0013464 OMIM:613855Orphanet:211067
- Causal genes
- CACNB4
- Part of
- Hereditary episodic ataxia
- Also known as
- CACNB4 hereditary episodic ataxia · EA5 · episodic ataxia, type 5 · hereditary episodic ataxia caused by mutation in CACNB4
Projects
No projects yet.