All diseases

OMIM ID
601952
OMIM term:
KERATOSIS LINEARIS WITH ICHTHYOSIS CONGENITA AND SCLEROSING KERATODERMA
Alternative terms:

(∗) Location:
13q12.3  
(†) Associated OMIM genes:
POMP  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/iuoc1yh7