All diseases

OMIM ID
168550
OMIM term:
PARIETAL FORAMINA WITH CLEIDOCRANIAL DYSPLASIA; PFMCCD
Alternative terms:

(∗) Location:
5q35.2  
(†) Associated OMIM genes:
MSX2  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/rlxbq7b5