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Summary Literature (1)
MIM:607876 - EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2; FAME2

Xenbase Genes: adra2b

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011930 - epilepsy, familial adult myoclonic, 2
MONDO:0019448 - benign adult familial myoclonic epilepsy

Disease Ontology (DO):
DOID:0111692 - familial adult myoclonic epilepsy 2