All diseases

OMIM ID
260660
OMIM term:
COUSIN SYNDROME
Alternative terms:
CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORT STATURE
PELVISCAPULAR DYSPLASIA
(∗) Location:
1p12  
(†) Associated OMIM genes:
TBX15  
(‡) Associated MGI genes:

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/cjua1ghh