epilepsy; Gene Set

Dataset	GAD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions. (Human Disease Ontology, DOID_1826)
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Genes

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

Symbol	Name
ABCB1	ATP-binding cassette, sub-family B (MDR/TAP), member 1
ABCC2	ATP-binding cassette, sub-family C (CFTR/MRP), member 2
CYP2C19	cytochrome P450, family 2, subfamily C, polypeptide 19
CYP2C8	cytochrome P450, family 2, subfamily C, polypeptide 8
CYP2C9	cytochrome P450, family 2, subfamily C, polypeptide 9
EPHX1	epoxide hydrolase 1, microsomal (xenobiotic)
SCN1A	sodium channel, voltage gated, type I alpha subunit
SCN1B	sodium channel, voltage gated, type I beta subunit
SCN2A	sodium channel, voltage gated, type II alpha subunit