All diseases

OMIM ID
302960
OMIM term:
CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2
Alternative terms:
CDPXD; CPXD
CONRADI-HUNERMANN SYNDROME
HAPPLE SYNDROME
CONRADI-HUNERMANN-HAPPLE SYNDROME
(∗) Location:
Xp11.23  
(†) Associated OMIM genes:
EBP  
(‡) Associated MGI genes:
Ebp   Nsdhl  

*Loading mouse genes ...

*Loading zebrafish genes ...

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