All diseases

OMIM ID
600513
OMIM term:
EPILEPSY, NOCTURNAL FRONTAL LOBE, TYPE 1
Alternative terms:

(∗) Location:
20q13.33  
(†) Associated OMIM genes:
CHRNA4  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/ritjghla