All diseases

OMIM ID
238970
OMIM term:
HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME
Alternative terms:
HHH SYNDROME; HHHS; HHH
ORNITHINE TRANSLOCASE DEFICIENCY
(∗) Location:
13q14.11  
(†) Associated OMIM genes:
SLC25A15  
(‡) 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/n5h4tnwi