All diseases

OMIM ID
612513
OMIM term:
CHROMOSOME 2p16.1-p15 DELETION SYNDROME
Alternative terms:

(∗) Location:
2p16.1-p15  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/fry92ki5