All diseases

OMIM ID
123150
OMIM term:
JACKSON-WEISS SYNDROME; JWS
Alternative terms:

(∗) Location:
10q26.13   8p11.23-p11.22  
(†) Associated OMIM genes:
FGFR1   FGFR2  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/w3jsriph