All diseases

OMIM ID
276902
OMIM term:
USHER SYNDROME, TYPE IIIA; USH3A
Alternative terms:

(∗) Location:
3q25.1  
(†) Associated OMIM genes:
CLRN1  
(‡) Associated MGI genes:
Clrn1  

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* quick link - http://q.sanger.ac.uk/r2wcmbh4