|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the Episodic ataxia type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
|KCNA1||potassium channel, voltage gated shaker related subfamily A, member 1|