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hy·per·or·ni·thin·emia (hi″pər-or″nĭ-thĭ-neґme-ə) excessive ornithine in the plasma, such as occurs in the genetic disorders gyrate atrophy of choroid and retina and hyperornithinemia-hyperammonemia-homocitrullinemia syndrome.Medical dictionary. 2011.
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
