Episodic Ataxia Type 2

About the Disease
Episodic Ataxia, Type 2, also known as episodic ataxia type 2, is related to familial hemiplegic migraine and hereditary ataxia, and has symptoms including ataxia, tinnitus and vertigo. An important gene associated with Episodic Ataxia, Type 2 is CACNA1A (Calcium Voltage-Gated Channel Subunit Alpha1 A), and among its related pathways/superpathways are ERK Signaling and MIF Mediated Glucocorticoid Regulation. The drugs Estradiol and Polyestradiol phosphate have been mentioned in the context of this disorder. Affiliated tissues include brain, cortex and cerebellum, and related phenotypes are nystagmus and ataxia

Common Targets
CACNA1A

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