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 — noun A metabolic disturbance characterized by excessive ammonia in the blood … Wiktionary
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