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Results 1 - 4 of 4 for Hyperornithinemia
  1. Ornithine translocase deficiency 
    ... of a substance called ornithine in the blood (hyperornithinemia) and the excretion of a substance called homocitrulline ... the condition. HHH syndrome ... syndrome Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome Triple ...
    https://medlineplus.gov/.../ornithine-translocase-deficiency - Genetics
  2. Gyrate atrophy of the choroid and retina 
    ... a result, excess ornithine accumulates in the blood (hyperornithinemia), and less P5C than normal is produced. It ... and symptoms of the condition. Gyrate atrophy HOGA Hyperornithinemia with gyrate atrophy of choroid and retina OAT ...
    https://medlineplus.gov/.../gyrate-atrophy-of-the-choroid-and-retina - Genetics
  3. SLC25A15 gene 
    ... of a human ORNT1 mutation (T32R) in the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome. Pediatr Res. 2006 Oct; ... rescue a defective ORNT1 in patients with the hyperornithinemia-hyperammonemia-homocitrullinuria syndrome, a urea cycle disorder. Mol ...
    https://medlineplus.gov/genetics/gene/slc25a15 - Genetics
  4. OAT gene 
    ... a result, excess ornithine accumulates in the blood (hyperornithinemia), and less P5C than normal is produced. It ... M, Ozawa K, Togari H. Vitamin B6-responsive ornithine aminotransferase deficiency with a novel mutation G237D. Tohoku J Exp ...
    https://medlineplus.gov/genetics/gene/oat - Genetics