All diseases

OMIM ID
605751
OMIM term:
SEIZURES, BENIGN FAMILIAL INFANTILE, 2; BFIS2
Alternative terms:

(∗) Location:
16p12-q12  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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