All diseases

OMIM ID
254600
OMIM term:
MYELOPEROXIDASE DEFICIENCY; MPOD
Alternative terms:

(∗) Location:
17q22  
(†) Associated OMIM genes:
MPO  
(‡) Associated MGI genes:
Mpo  

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