All diseases

OMIM ID
265000
OMIM term:
MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS
Alternative terms:
ESCOBAR SYNDROME
MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE
PTERYGIUM SYNDROME
MULTIPLE PTERYGIUM SYNDROME
PTERYGIUM COLLI SYNDROME
PTERYGIUM UNIVERSALE
(∗) Location:
2q37.1  
(†) Associated OMIM genes:
CHRNG  
(‡) 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/sjaeqnth