All diseases

OMIM ID
139393
OMIM term:
GUILLAIN-BARRE SYNDROME, FAMILIAL; GBS
Alternative terms:

(∗) Location:
17p12  
(†) Associated OMIM genes:
PMP22  
(‡) Associated MGI genes:
Cd86  

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/wcjzvx7h