All diseases

OMIM ID
148210
OMIM term:
KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT
Alternative terms:

(∗) Location:
13q12.11  
(†) Associated OMIM genes:
GJB2  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/n42zrfts