All diseases

OMIM ID
608233
OMIM term:
HERMANSKY-PUDLAK SYNDROME 2; HPS2
Alternative terms:

(∗) Location:
5q14.1  
(†) Associated OMIM genes:
AP3B1  
(‡) Associated MGI genes:
Ap3b1   Ap3d1  

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/226zk991