All diseases

OMIM ID
216400
OMIM term:
COCKAYNE SYNDROME, TYPE A; CSA
Alternative terms:

(∗) Location:
5q12.1  
(†) Associated OMIM genes:
ERCC8  
(‡) 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/ctsthd96