Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 2 of 2 for "Hyperornithinemia-hyperammonemia-homocitrullinuria%syndrome"
  1. Ornithine translocase deficiency 
    ... not show signs and symptoms of the condition. HHH syndrome Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome ...
    https://medlineplus.gov/.../ornithine-translocase-deficiency - Genetics
  2. SLC25A15 gene 
    ... ORNT1 mutation (T32R) in the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome. Pediatr Res. 2006 Oct;60(4):423-9. ... rescue a defective ORNT1 in patients with the hyperornithinemia-hyperammonemia-homocitrullinuria syndrome, a urea cycle disorder. Mol Genet Metab. 2003 ...
    https://medlineplus.gov/genetics/gene/slc25a15 - Genetics