All diseases

OMIM ID
600257
OMIM term:
CHROMOSOME 8q12.1-q21.2 DELETION SYNDROME
Alternative terms:

(∗) Location:
8q12.2-q21.2  
(†) 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/48t3ps5u