All diseases

OMIM ID
218030
OMIM term:
APPARENT MINERALOCORTICOID EXCESS; AME
Alternative terms:
AME1
CORTISOL 11-BETA-KETOREDUCTASE DEFICIENCY
(∗) Location:
16q22.1  
(†) Associated OMIM genes:
HSD11B2  
(‡) Associated MGI genes:
Hsd11b2  

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* quick link - http://q.sanger.ac.uk/557l5i07