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Summary Literature (1)
MIM:611942 - EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 6; ECA6

Xenbase Genes: cacna1h

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010826 - childhood absence epilepsy
MONDO:0012763 - epilepsy, childhood absence, susceptibility to, 6