hyperammonemia

hyperammonemia
A metabolic disturbance characterized by excessive ammonia in the blood.

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  • Hyperammonemia — Infobox Disease Name = PAGENAME Caption = Ammonia DiseasesDB = 20468 ICD10 = ICD10|E|72|2|e|70 ICD9 = ICD9|270.6 ICDO = OMIM = MedlinePlus = eMedicineSubj = neuro eMedicineTopic = 162 eMedicine mult = eMedicine2|ped|1057 | MeshID = D022124… …   Wikipedia

  • hyperammonemia — ▪ metabolic disorder       disorder due to excessive amounts of ammonia in the blood caused by a genetic defect present at birth, by a genetic defect acquired in adulthood, or by liver disease. Ammonia is metabolized by the liver to produce a… …   Universalium

  • hyperammonemia — SYN: ammonemia. * * * hy·per·am·mo·ne·mia .hī pə .ram ə nē mē ə also hy·per·am·mon·i·emia .hī pə rə .mō nē yē mē ə or chiefly Brit hy·per·am·mo·nae·mia also hy·per·am·mon·i·ae·mia n the presence of an excess of ammonia in the blood… …   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

  • cerebroatrophic hyperammonemia — Rett syndrome …   Medical dictionary

  • Ammonia — For other uses, see Ammonia (disambiguation). Ammonia …   Wikipedia

  • Valproic acid — Systematic (IUPAC) name 2 propylpentanoic …   Wikipedia

  • Lysinuric protein intolerance — Classification and external resources Lysine ICD 10 E …   Wikipedia

  • N-Acetylglutamate synthase deficiency — Classification and external resources N Acetylglutamic acid OMIM 237310 …   Wikipedia

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

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