All diseases

OMIM ID
602083
OMIM term:
USHER SYNDROME, TYPE IF; USH1F
Alternative terms:

(∗) Location:
10q21.1  
(†) Associated OMIM genes:
PCDH15  
(‡) Associated MGI genes:
Pcdh15  

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/uypc22dm