All diseases

OMIM ID
602097
OMIM term:
USHER SYNDROME, TYPE IE; USH1E
Alternative terms:

(∗) Location:
21q21  
(†) 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/scshbdo4