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Summary Literature (0)
MIM:618074 - EPILEPSY, FAMILIAL ADULT MYOCLONIC, 6; FAME6

Xenbase Genes: tnrc6a

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0054846 - epilepsy, familial adult myoclonic, 6

Disease Ontology (DO):
DOID:0111696 - familial adult myoclonic epilepsy 6