argininosuccinic acidemia

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• Argininosuccinic aciduria — Infobox Disease Name = PAGENAME Caption = argininosuccinate DiseasesDB = ICD10 = ICD10|E|72|2|e|70 ICD9 = ICD9|270.6 ICDO = OMIM = 207900 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Argininosuccinic aciduria, also called… …   Wikipedia

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• D-Glyceric acidemia — Classification and external resources OMIM 220120 D Glyceric Acidemia (a.k.a. D Glyceric Aciduria) is an inherited disease, in the category of inborn errors of metabolism. It is caused by a mutation in the gene GLYCTK, which encodes the for the… …   Wikipedia

• Organic acidemia — Organic acidemia, also called organic aciduria, is a term used to classify a group of metabolic disorders which disrupt normal amino acid metabolism, particularly branched chain amino acids, causing a buildup of acids which are usually not… …   Wikipedia

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• Newborn screening — See also: Apgar score Newborn screening Intervention MeSH D015997 Newborn screening is the process by which infants are screened shortly after birth for a list of disorders that are treatable, but di …   Wikipedia

• 3-Methylglutaconic aciduria — Classification and external resources 3 methylglutaconic acid DiseasesDB …   Wikipedia

• Methylmalonyl-CoA mutase deficiency — Classification and external resources OMIM 251000 DiseasesDB 29509 Methylmalonyl CoA mutase deficiency ( MUT ) is an inborn error of organ …   Wikipedia