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Summary Literature (2)
MIM:616187 - EPILEPSY, PROGRESSIVE MYOCLONIC 7; EPM7

Xenbase Genes: kcnc1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014521 - progressive myoclonic epilepsy type 7

Disease Ontology (DO):
DOID:0111447 - progressive myoclonus epilepsy 7