All diseases

OMIM ID
121200
OMIM term:
SEIZURES, BENIGN FAMILIAL NEONATAL, 1; BFNS1 EPILEPSY, BENIGN NEONATAL, 1, AND/OR MYOKYMIA, INCLUDED
Alternative terms:

(∗) Location:
20q13.33  
(†) Associated OMIM genes:
KCNQ2  
(‡) Associated MGI genes:
Kcnq2  

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* quick link - http://q.sanger.ac.uk/g0q6fa11