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Summary Literature (0)
MIM:617935 - EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 4; FFEVF4

Xenbase Genes: scn3a

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0054776 - epilepsy, familial focal, with variable foci 4

Disease Ontology (DO):
DOID:0081424 - familial focal epilepsy with variable foci 4