All diseases

OMIM ID
166990
OMIM term:
OSTEOCHONDRODYSPLASIA, RHIZOMELIC, WITH CALLOSAL AGENESIS, THROMBOCYTOPENIA, HYDROCEPHALUS, AND HYPERTENSION
Alternative terms:

(∗) Location:
(†) Associated OMIM genes:
(‡) Associated MGI genes:
Nfix  

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/9cvpw7ps