All diseases

OMIM ID
268100
OMIM term:
ENHANCED S-CONE SYNDROME; ESCS GOLDMANN-FAVRE SYNDROME, INCLUDED
Alternative terms:
RETINOSCHISIS WITH EARLY HEMERALOPIA, INCLUDED
FAVRE HYALOIDEORETINAL DEGENERATION, INCLUDED
(∗) Location:
15q23  
(†) Associated OMIM genes:
NR2E3  
(‡) Associated MGI genes:
Nr2e3  

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/942za19b