All diseases

OMIM ID
601067
OMIM term:
USHER SYNDROME, TYPE ID; USH1D USHER SYNDROME, TYPE ID/F, CDH23/PCDH15, DIGENIC, INCLUDED
Alternative terms:

(∗) Location:
10q21.1   10q22.1  
(†) Associated OMIM genes:
CDH23   PCDH15  
(‡) Associated MGI genes:
Cdh23  

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* quick link - http://q.sanger.ac.uk/55cay4e6