All diseases

OMIM ID
607624
OMIM term:
GRISCELLI SYNDROME, TYPE 2; GS2
Alternative terms:
GRISCELLI SYNDROME WITH HEMOPHAGOCYTIC SYNDROME
PARTIAL ALBINISM AND IMMUNODEFICIENCY SYNDROME
PAID SYNDROME
(∗) Location:
15q21.3  
(†) Associated OMIM genes:
RAB27A  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/kuapfaol