ornithine translocase deficiency (Q7103627)

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amino acid metabolic disorder that has material basis in deficiency of ornithine translocase resulting in the accumulation of ammonia in the blood
  • HHH syndrome
  • Hyperornithinemia-Hyperammonemia-Homocitrullinuria (HHH) syndrome
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Language Label Description Also known as
English
ornithine translocase deficiency
amino acid metabolic disorder that has material basis in deficiency of ornithine translocase resulting in the accumulation of ammonia in the blood
  • HHH syndrome
  • Hyperornithinemia-Hyperammonemia-Homocitrullinuria (HHH) syndrome

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