All diseases

OMIM ID
162830
OMIM term:
NEUTROPHILIA, HEREDITARY
Alternative terms:

(∗) Location:
1p34.3  
(†) Associated OMIM genes:
CSF3R  
(‡) Associated MGI genes:
Csf3r  

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* quick link - http://q.sanger.ac.uk/i4xmt9q8