Episodic ataxia type 1 Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Episodic ataxia type 1 (EA1) is a frequent form of Hereditary episodic ataxia (EA; see this term) characterized by brief episodes of ataxia, neuromyotonia, and continuous interictal myokymia. (Orphanet Rare Disease Ontology, Orphanet_37612)
External Link http://www.omim.org/entry/160120
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1 genes associated with the Episodic ataxia type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
KCNA1 potassium channel, voltage gated shaker related subfamily A, member 1