All diseases

OMIM ID
309583
OMIM term:
MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE; MRXSSR
Alternative terms:

(∗) Location:
Xp22.11  
(†) Associated OMIM genes:
SMS  
(‡) Associated MGI genes:

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/ateo7iox