All diseases

OMIM ID
310465
OMIM term:
N SYNDROME; NSX
Alternative terms:

(∗) Location:
Xp22.1-p21.3  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/nday28wl