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Summary Literature (0)
MIM:618075 - EPILEPSY, FAMILIAL ADULT MYOCLONIC, 7; FAME7

Xenbase Genes: rapgef2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0054847 - epilepsy, familial adult myoclonic, 7

Disease Ontology (DO):
DOID:0111694 - familial adult myoclonic epilepsy 7