All diseases

OMIM ID
308240
OMIM term:
LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1; XLP1
Alternative terms:
XLP
LYMPHOPROLIFERATIVE DISEASE, X-LINKED; XLPD
LYP
DUNCAN DISEASE
EPSTEIN-BARR VIRUS INFECTION, FAMILIAL FATAL
EBV INFECTION, SEVERE, SUSCEPTIBILITY TO; EBVS
INFECTIOUS MONONUCLEOSIS, SEVERE, SUSCEPTIBILITY TO
IMMUNODEFICIENCY, X-LINKED PROGRESSIVE COMBINED VARIABLE
IMMUNODEFICIENCY 5; IMD5
PURTILO SYNDROME
(∗) Location:
Xq25  
(†) Associated OMIM genes:
SH2D1A  
(‡) Associated MGI genes:
Sh2d1a  

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/vnj5arpc