All diseases

OMIM ID
193300
OMIM term:
VON HIPPEL-LINDAU SYNDROME; VHL VON HIPPEL-LINDAU SYNDROME, MODIFIERS OF, INCLUDED
Alternative terms:

(∗) Location:
11q13.3   3p25.3  
(†) Associated OMIM genes:
CCND1   VHL  
(‡) Associated MGI genes:
Vhl  

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/nekog1va