All diseases

OMIM ID
302200
OMIM term:
CATARACT, CONGENITAL, X-LINKED; CXN
Alternative terms:

(∗) Location:
Xp22.13  
(†) Associated OMIM genes:
NHS  
(‡) 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/3np2lsv0