- ornithine carbamoyl phosphate deficiency
- عوز فسفات كربامويل الأورنيثين
English-Arabic Medical Dictionary. 2013.
ornithine carbamoyl phosphate deficiency
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Carbamoyl phosphate synthetase I — Protein Name=carbamoyl phosphate synthetase 1, mitochondrial caption= Symbol=CPS1 AltSymbols= HGNCid=2323 Chromosome=2 Arm=p Band= LocusSupplementaryData= ECnumber=6.3.4.16 OMIM=608307 EntrezGene=1373 RefSeq=NM 001875 UniProt=P31327 PDB=Carbamoyl … Wikipedia
carbamoyl phosphate — A reactive intermediate capable of transferring its carbamoyl group to an acceptor molecule, forming citrulline from ornithine in the urea cycle, and ureidosuccinic acid from aspartic acid in … Medical dictionary
Ornithine transcarbamylase — Ornithine carbamoyltransferase Human OTC trimer. From PDB 1OTH … Wikipedia
Ornithine transcarbamylase deficiency — Classification and external resources Ornithine ICD 10 E … Wikipedia
Ornithine translocase deficiency — Classification and external resources Ornithine ICD 9 … Wikipedia
Ornithine translocase — solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15 Identifiers Symbol SLC25A15 Alt. symbols ORNT1, HHH Entrez … Wikipedia
ornithine — 2,5 Diaminovaleric acid; the l isomer is the amino acid formed when l arginine is hydrolyzed by arginase; not a constituent of proteins, but an important intermediate in the urea cycle; elevated levels seen in certain defects of the urea cycle. o … Medical dictionary
N-Acetylglutamate synthase deficiency — Classification and external resources N Acetylglutamic acid OMIM 237310 … Wikipedia
Glutathione synthetase deficiency — Classification and external resources Glutathione OMIM 266130 … Wikipedia
Beta-ketothiolase deficiency — Classification and external resources Isoleucine OMIM 203750 … Wikipedia
3-Methylcrotonyl-CoA carboxylase deficiency — Classification and external resources Methylcrotonyl CoA OMIM 210200 … Wikipedia
