All diseases

OMIM ID
610706
OMIM term:
DEAFNESS, CONGENITAL, WITH INNER EAR AGENESIS, MICROTIA, AND MICRODONTIA
Alternative terms:
DEAFNESS, CONGENITAL, WITH LABYRINTHINE APLASIA, MICROTIA, AND MICRODONTIA
DEAFNESS WITH LAMM
(∗) Location:
11q13.3  
(†) Associated OMIM genes:
FGF3  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/dk6bmzxq