All diseases

OMIM ID
167210
OMIM term:
PACHYONYCHIA CONGENITA, TYPE 2; PC2
Alternative terms:

(∗) Location:
12q13.13   17q21.2  
(†) Associated OMIM genes:
KRT17   KRT6B  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/u3wupjmy