All diseases

OMIM ID
613026
OMIM term:
CHROMOSOME 19q13.11 DELETION SYNDROME
Alternative terms:

(∗) Location:
19q13.11  
(†) Associated OMIM genes:
(‡) 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/gwk14ppl