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Summary Literature (0)
MIM:617116 - EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 2; FFEVF2

Xenbase Genes: nprl2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014924 - epilepsy, familial focal, with variable foci 2
MONDO:0020310 - familial focal epilepsy with variable foci

Disease Ontology (DO):
DOID:0081422 - familial focal epilepsy with variable foci 2