All diseases

OMIM ID
201400
OMIM term:
ACTH DEFICIENCY, ISOLATED; IAD
Alternative terms:

(∗) Location:
1q24.2  
(†) Associated OMIM genes:
TBX19  
(‡) Associated MGI genes:
Tbx19  

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/cqz82ytq