All diseases

OMIM ID
261800
OMIM term:
PIERRE ROBIN SYNDROME
Alternative terms:
GLOSSOPTOSIS, MICROGNATHIA, AND CLEFT PALATE
PIERRE ROBIN SEQUENCE
(∗) Location:
17q24.3-q25.1  
(†) Associated OMIM genes:
(‡) Associated MGI genes:
Acvr2a   hpmd  

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/8hfqijvd