All diseases

OMIM ID
276900
OMIM term:
USHER SYNDROME, TYPE I; USH1
Alternative terms:
US1
RETINITIS PIGMENTOSA AND CONGENITAL DEAFNESS USHER SYNDROME, TYPE IB, INCLUDED; USH1B, INCLUDED
USHER SYNDROME, TYPE IA, FORMERLY, INCLUDED; USH1A, FORMERLY, INCLUDED
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY, INCLUDED
(∗) Location:
11q13.5  
(†) Associated OMIM genes:
MYO7A  
(‡) Associated MGI genes:
Myo7a  

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