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Summary Literature (0)
MIM:601068 - EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1; FAME1

Xenbase Genes: samd12

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010985 - epilepsy, familial adult myoclonic, 1

Disease Ontology (DO):
DOID:0111690 - familial adult myoclonic epilepsy 1