All diseases

OMIM ID
602092
OMIM term:
DEAFNESS, AUTOSOMAL RECESSIVE 18; DFNB18
Alternative terms:

(∗) Location:
11p15.1  
(†) Associated OMIM genes:
USH1C  
(‡) Associated MGI genes:
Ush1c  

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* quick link - http://q.sanger.ac.uk/e406euad