All diseases

OMIM ID
124500
OMIM term:
DEAFNESS, CONGENITAL, WITH KERATOPACHYDERMIA AND CONSTRICTIONS OF FINGERS AND TOES
Alternative terms:
VOHWINKEL SYNDROME
MUTILATING KERATODERMA
KERATODERMA HEREDITARIUM MUTILANS; KHM
(∗) Location:
13q12.11  
(†) Associated OMIM genes:
GJB2  
(‡) Associated MGI genes:

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/kezzpmi9