All diseases

OMIM ID
610353
OMIM term:
EPILEPSY, NOCTURNAL FRONTAL LOBE, TYPE 4
Alternative terms:
ENFL4
EPILEPSY, FAMILIAL, WITH NOCTURNAL WANDERING AND ICTAL FEAR
(∗) Location:
8p21.2  
(†) Associated OMIM genes:
CHRNA2  
(‡) Associated MGI genes:

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