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Summary Literature (1)
MIM:615400 - EPILEPSY, FAMILIAL ADULT MYOCLONIC, 5; FAME5

Xenbase Genes: cntn2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014167 - epilepsy, familial adult myoclonic, 5
MONDO:0019448 - benign adult familial myoclonic epilepsy

Disease Ontology (DO):
DOID:0111691 - familial adult myoclonic epilepsy 5