episodic ataxia, type 5 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Episodic ataxia type 5 (EA5) is an extremely rare form of Hereditary episodic ataxia (see this term) characterized by recurrent episodes of vertigo and ataxia lasting several hours. (Orphanet Rare Disease Ontology, Orphanet_211067)
External Link http://www.omim.org/entry/613855
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1 genes associated with the episodic ataxia, type 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
CACNB4 calcium channel, voltage-dependent, beta 4 subunit