All diseases

OMIM ID
609597
OMIM term:
PARIETAL FORAMINA 2; PFM2
Alternative terms:

(∗) Location:
11p11.2  
(†) Associated OMIM genes:
ALX4  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/3eokp9el