|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the episodic ataxia, type 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
|CACNB4||calcium channel, voltage-dependent, beta 4 subunit|