All diseases

OMIM ID
300299
OMIM term:
NEUTROPENIA, SEVERE CONGENITAL, X-LINKED; SCNX
Alternative terms:

(∗) Location:
Xp11.23  
(†) Associated OMIM genes:
WAS  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/2502cyuz