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Summary Literature (0)
MIM:600669 - EPILEPSY, IDIOPATHIC GENERALIZED; EIG

Xenbase Genes: me2, oprm1, cacnb4

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010918 - epilepsy, idiopathic generalized, susceptibility to, 1

Disease Ontology (DO):
DOID:1827 - idiopathic generalized epilepsy