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Summary Literature (0)
MIM:612269 - EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5; ECA5

Xenbase Genes: gabrb3

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010826 - childhood absence epilepsy
MONDO:0012843 - epilepsy, childhood absence, susceptibility to, 5