hyperornithinemia

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• hyperornithinemia — Elevated levels of ornithine in the serum; sometimes associated with hyperammonemia and homocitrullinuria. * * * hy·per·or·ni·thin·emia (hi″pər or″nĭ thĭ neґme ə) excessive ornithine in the plasma, such as occurs… …   Medical dictionary

• hyperornithinemia-hyperammonemia-homocitrullinuria syndrome — an autosomal recessive syndrome characterized by elevated plasma levels of ornithine, postprandial hyperammonemia and homocitrullinuria, and aversion to protein ingestion. It is believed to result from a defect in the transport of ornithine into… …   Medical dictionary

• HHH — hyperornithinemia, hyperammonemia, homocitrillinuria [syndrome] …   Medical dictionary

• HOGA — hyperornithinemia with gyrate atrophy …   Medical dictionary

• HHH syndrome — hyperornithinemia hyperammonemia homocitrullinuria s …   Medical dictionary

• HHH — • hyperornithinemia, hyperammonemia, homocitrillinuria [syndrome] …   Dictionary of medical acronyms & abbreviations

• HOGA — • hyperornithinemia with gyrate atrophy …   Dictionary of medical acronyms & abbreviations

• Iminoglycinuria — Classification and external resources Imine, a functional group found in imino acids ICD 10 E72.0 …   Wikipedia

• List of diseases (H) — A list of diseases in the English wikipedia.DiseasesTOC HaHag Ham* Hageman factor deficiency * Hagemoser Weinstein Bresnick syndrome * Hailey Hailey disease * Hair defect with photosensitivity and mental retardation * Hairy cell leukemia * Hairy… …   Wikipedia

• Ornithine translocase deficiency — Classification and external resources Ornithine ICD 9 …   Wikipedia

• Mitochondrieller Ornithin-Transporter — 1 Masse/Länge Primärstruktur 301 Aminosäuren …   Deutsch Wikipedia