All diseases

OMIM ID
605472
OMIM term:
USHER SYNDROME, TYPE IIC; USH2C USHER SYNDROME, TYPE IIC, GPR98/PDZD7, DIGENIC, INCLUDED
Alternative terms:

(∗) Location:
10q24.31   5q14.3  
(†) Associated OMIM genes:
GPR98   PDZD7  
(‡) Associated MGI genes:
Gpr98   Slc4a7  

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