All diseases

OMIM ID
607745
OMIM term:
SEIZURES, BENIGN FAMILIAL INFANTILE, 3; BFIS3
Alternative terms:
CONVULSIONS, BENIGN FAMILIAL INFANTILE, 3; BFIC3
SEIZURES, BENIGN FAMILIAL NEONATAL-INFANTILE; BFNIS
(∗) Location:
2q24.3  
(†) Associated OMIM genes:
SCN2A  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/ba9wcgp8