myokymia Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Successive and rapid contractions of motor units associated with chronic nerve injury. The discharges arise from the peripheral aspects of regenerating nerves, and clinically impart a nearly continuous undulation of the body surface overlying the muscle. (Human Phenotype Ontology, HP_0002411)
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1 genes associated with the myokymia phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
KCNQ2 potassium channel, voltage gated KQT-like subfamily Q, member 2