All diseases

OMIM ID
602849
OMIM term:
MUENKE SYNDROME; MNKES
Alternative terms:

(∗) Location:
4p16.3  
(†) Associated OMIM genes:
FGFR3  
(‡) Associated MGI genes:
Fgfr3  

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/8e317oz2