All diseases

OMIM ID
613038
OMIM term:
PITUITARY HORMONE DEFICIENCY, COMBINED, 1; CPHD1
Alternative terms:

(∗) Location:
3p11.2  
(†) Associated OMIM genes:
POU1F1  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/p087tgxq