All diseases

OMIM ID
601553
OMIM term:
HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY; HJMD
Alternative terms:

(∗) Location:
16q22.1  
(†) Associated OMIM genes:
CDH3  
(‡) 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/se74wuxg