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Summary Literature (0)
MIM:607628 - EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 11; EIG11

Xenbase Genes: clcn2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009696 - juvenile myoclonic epilepsy
MONDO:0011875 - epilepsy, idiopathic generalized, susceptibility to, 11