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Summary Literature (10)
DOID:1827 - idiopathic generalized epilepsy


Disease Ontology Definition:An epilepsy syndrome that is characterised by generalised seizures with no apparent cause which arise from many independent foci (multifocal epilepsies) or from epileptic circuits that involve the whole brain.

Synonyms: Generalised epilepsy

Xenbase Genes : me2, hcn1, chd2, scn1a, scn1b, oprm1, cacnb4, gabrg2, stx1b, scn2a

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0005579 - epilepsy, idiopathic generalized

OMIM:
OMIM:600669 - EPILEPSY, IDIOPATHIC GENERALIZED; EIG

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): epilepsy (is_a)