All diseases

OMIM ID
272120
OMIM term:
SUDDEN INFANT DEATH SYNDROME
Alternative terms:

(∗) Location:
3p22.2  
(†) Associated OMIM genes:
SCN5A  
(‡) Associated MGI genes:
Slc6a4  

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* quick link - http://q.sanger.ac.uk/vnojjrh6