ornithine translocase deficiency (Q7103627)

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An 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
An 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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