All diseases

OMIM ID
177200
OMIM term:
LIDDLE SYNDROME
Alternative terms:

(∗) Location:
16p12.2  
(†) Associated OMIM genes:
SCNN1B   SCNN1G  
(‡) Associated MGI genes:
Scnn1b  

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/gv5688a1