All diseases

OMIM ID
180750
OMIM term:
ROBINOW-SORAUF SYNDROME
Alternative terms:
CRANIOSYNOSTOSIS-BIFID HALLUX SYNDROME
ACROCEPHALOSYNDACTYLY, ROBINOW-SORAUF TYPE
(∗) Location:
7p21.1  
(†) Associated OMIM genes:
TWIST1  
(‡) 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/h1zgr81b