short-chain acyl-CoA dehydrogenase

See acyl-CoA dehydrogenase (NADPH).

Medical dictionary. 2011.

Look at other dictionaries:

  • short-chain acyl-CoA dehydrogenase (SCAD) deficiency — a defect in mitochondrial beta oxidation due to a mutation in the gene (locus: 12q22 qter) encoding the acyl CoA dehydrogenase that acts on short chain length fatty acids. Clinical presentation is variable, but myopathy and abnormalities of… …   Medical dictionary

  • Short-chain acyl-coenzyme A dehydrogenase deficiency — DiseaseDisorder infobox Name = PAGENAME ICD10 = ICD9 = ICD9|277.85 ICDO = Caption = OMIM = 201470 MedlinePlus = eMedicineSubj = eMedicineTopic = DiseasesDB = 31599 Short chain acyl coenzyme A dehydrogenase deficiency (or SCADD ) is a fatty acid… …   Wikipedia

  • Butyryl-CoA dehydrogenase — In enzymology, a butyryl CoA dehydrogenase (EC number|1.3.99.2) is an enzyme that catalyzes the chemical reaction:butanoyl CoA + acceptor ightleftharpoons 2 butenoyl CoA + reduced acceptorThus, the two substrates of this enzyme are butanoyl CoA… …   Wikipedia

  • Medium-chain acyl-coenzyme A dehydrogenase deficiency — (MCAD) Classification and external resources ICD 9 277.85 OMIM 201450 …   Wikipedia

  • Butyryl CoA dehydrogenase — protein Name=acyl Coenzyme A dehydrogenase, C 2 to C 3 short chain caption= width= HGNCid=90 Symbol=ACADS AltSymbols= EntrezGene=35 OMIM=606885 RefSeq=NM 000017 UniProt=P16219 PDB= ECnumber=1.3.99.2 Chromosome=12 Arm=q Band=24.31… …   Wikipedia

  • Malonyl-CoA decarboxylase deficiency — Classification and external resources Malonyl CoA OMIM 248360 …   Wikipedia

  • Acil-CoA deshidrogenasa — de cadena muy larga HUGO 92 Símbolo ACADVL Datos genéticos …   Wikipedia Español

  • Propionyl-CoA carboxylase — PCCA redirects here. For other uses, see PCCA (disambiguation). Propionyl CoA carboxylase Identifiers EC number 6.4.1.3 CAS number …   Wikipedia

  • 2,4 Dienoyl-CoA reductase deficiency — Classification and external resources OMIM 222745 2,4 Dienoyl CoA reductase deficiency is a fatty acid metabolism disorder. It occurs on as a result of a mutation on Chromosome 8. See also 2,4 Dienoyl CoA reductase …   Wikipedia

  • 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

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