All diseases

OMIM ID
168500
OMIM term:
PARIETAL FORAMINA; PFM
Alternative terms:
PARIETAL FORAMINA, SYMMETRIC
FORAMINA PARIETALIA PERMAGNA; FPP
CATLIN MARKS
CRANIUM BIFIDUM OCCULTUM
CRANIUM BIFIDUM, HEREDITARY PARIETAL FORAMINA 1, INCLUDED; PFM1, INCLUDED
(∗) Location:
5q35.2  
(†) Associated OMIM genes:
MSX2  
(‡) Associated MGI genes:
Msx2  

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/vt27vuwm