acylcarnitine

Medical dictionary. 2011.

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  • Acylcarnitine hydrolase — In enzymology, an acylcarnitine hydrolase (EC number|3.1.1.28) is an enzyme that catalyzes the chemical reaction:O acylcarnitine + H2O ightleftharpoons a fatty acid + L carnitineThus, the two substrates of this enzyme are O acylcarnitine and H2O …   Wikipedia

  • Carnitine-acylcarnitine translocase — protein Name=solute carrier family 25 (carnitine/acylcarnitine translocase), member 20 caption= width= HGNCid=1421 Symbol=SLC25A20 AltSymbols=CACT EntrezGene=788 OMIM=212138 RefSeq=NM 000387 UniProt=O43772 PDB= ECnumber= Chromosome=3 Arm=p… …   Wikipedia

  • Carnitine-acylcarnitine translocase deficiency — DiseaseDisorder infobox Name = Carnitine acylcarnitine translocase deficiency ICD10 = ICD9 = ICD9|272.8 Carnitine acylcarnitine translocase deficiency is a rare, autosomal recessive metabolic disorder that prevents the body from converting long… …   Wikipedia

  • Carnitine — Systematic (IUPAC) name 3 hydroxy 4 (trimethylazaniumyl)butanoate Clinical data AHFS/Drugs.com …   Wikipedia

  • Carnitine palmitoyltransferase II deficiency — Classification and external resources Carnitine ICD 9 …   Wikipedia

  • Pathophysiology of chronic fatigue syndrome — The pathogenesis of chronic fatigue syndrome (CFS) is uncertain, but may involve multiple organ and body systems, including neurological, endocrinal and immunological factors.Nervous system factorsNeurological abnormalitiesCFS may involve… …   Wikipedia

  • muscle disease — ▪ pathology Introduction       any of the diseases and disorders that affect the human muscle system (muscle system, human). Diseases and disorders that result from direct abnormalities of the muscles are called primary muscle diseases; those… …   Universalium

  • Inborn error of lipid metabolism — Classification and external resources Several fatty acid molecules ICD 10 E75 …   Wikipedia

  • Inborn errors of lipid metabolism — ICD9|277.85 ICDO = OMIM = MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = D008052 Numerous genetic disorders are caused by errors in fatty acid metabolism. These disorders may be described as fatty oxidation disorders or as a lipid… …   Wikipedia

  • Chromosome 3 (human) — Short and long arms Chromosome 3 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 3 spans almost 200 million base pairs (the building material of DNA) and represents about 6.5 percent …   Wikipedia

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