All diseases

OMIM ID
175200
OMIM term:
PEUTZ-JEGHERS SYNDROME; PJS
Alternative terms:
POLYPOSIS, HAMARTOMATOUS INTESTINAL
POLYPS-AND-SPOTS SYNDROME
(∗) Location:
19p13.3  
(†) Associated OMIM genes:
STK11  
(‡) Associated MGI genes:
Stk11  

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/dtp9ecct