All diseases

OMIM ID
182230
OMIM term:
SEPTOOPTIC DYSPLASIA
Alternative terms:
DE MORSIER SYNDROME PITUITARY HORMONE DEFICIENCY, COMBINED, 5, INCLUDED; CPHD5, INCLUDED
GROWTH HORMONE DEFICIENCY WITH PITUITARY ANOMALIES, INCLUDED
(∗) Location:
3p14.3  
(†) Associated OMIM genes:
HESX1  
(‡) Associated MGI genes:
Hesx1  

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/bxx38yj0