Medical dictionary. 2011.
Prolidase deficiency — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 29838 ICD10 = ICD9 = ICDO = OMIM = 170100 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Prolidase deficiency is a rare autosomal recessive [cite journal |pmid=7187192 |year=1982… … Wikipedia
Ornithine transcarbamylase deficiency — Classification and external resources Ornithine ICD 10 E … Wikipedia
3-Methylcrotonyl-CoA carboxylase deficiency — Classification and external resources Methylcrotonyl CoA OMIM 210200 … Wikipedia
Glutathione synthetase deficiency — Classification and external resources Glutathione OMIM 266130 … Wikipedia
Ornithine translocase deficiency — Classification and external resources Ornithine ICD 9 … Wikipedia
Guanidinoacetate methyltransferase deficiency — Classification and external resources Glycocyamine OMIM 601240 … Wikipedia
Dopamine beta hydroxylase deficiency — Classification and external resources Dopamine beta hydroxylase is the enzyme responsible for converting dopamine (pictured) to norepinephrine. OMIM … Wikipedia
Beta-ketothiolase deficiency — Classification and external resources Isoleucine OMIM 203750 … Wikipedia
N-Acetylglutamate synthase deficiency — Classification and external resources N Acetylglutamic acid OMIM 237310 … 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
