juvenile myoclonic epilepsy Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A adolescence-adult electroclinical syndrome that is characterized by brief, involuntary twitching of a muscle or a group of muscles (myoclonus) early in the morning with onset between 12 and 18 years. (Human Disease Ontology, DOID_4890)
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Genes

2 genes associated with the disease juvenile myoclonic epilepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
BRD2 bromodomain containing 2
KCNQ3 potassium channel, voltage gated KQT-like subfamily Q, member 3