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Summary Literature (0)
MIM:611726 - EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS; EPM3

Xenbase Genes: kctd7

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012721 - progressive myoclonic epilepsy type 3

Disease Ontology (DO):
DOID:0111446 - progressive myoclonus epilepsy 3
DOID:891 - progressive myoclonus epilepsy