All diseases

OMIM ID
227260
OMIM term:
SETLEIS SYNDROME
Alternative terms:
FACIAL ECTODERMAL DYSPLASIA
BITEMPORAL FORCEPS MARKS SYNDROME
FOCAL FACIAL DERMAL DYSPLASIA, TYPE II
FFDD, TYPE II
(∗) Location:
2q37.3  
(†) Associated OMIM genes:
TWIST2  
(‡) Associated MGI genes:
Twist2  

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/xlwyh0a0