All diseases

OMIM ID
606943
OMIM term:
USHER SYNDROME, TYPE IG; USH1G
Alternative terms:

(∗) Location:
17q25.1  
(†) Associated OMIM genes:
USH1G  
(‡) Associated MGI genes:
Ush1g  

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* quick link - http://q.sanger.ac.uk/m4dy935l