17 beta hydroxysteroid dehydrogenaseABCD1ABCD2ABCD3 GCP60 PAP7 GOCAP1 GOLPH1ACAA1 Acetyl CoA acyltransferase1ACAA2 MCKAT medium chain 3 ketoacyl CoA thiolaseACAD11 Acyl CoA dehydrogenase11ACAD9ACADM MCAD Medium chain acyl CoA dehydrogenase deficiencyACADS SCAD short chain acyl CoA dehydrogenaseACADVL VLCAD Very long chain acyl CoA synthetaseACC1 Acetyl CoA carboxylase1ACNAT1 Acyl CoA amino acid N acyltransferaseACOT12 Acyl CoA thioesterase12ACOT2 Acyl CoA thioesterase2ACOT4 Acyl CoA thioesterase4ACOT6 Acyl CoA thioesterase6ACOT8 Acyl CoA thioesterase8ACOX1 Acyl CoA oxidase1a 1bACOX2 Acyl CoA oxidase2ACOX3 Acyl CoA oxidase3ACOXIACOXL Acyl CoA oxidase likeACSL1 Acyl CoA synthetase long chain1ACSL4 Acyl CoA synthetase long chain4Adrenoleukodystrophy pseudoneonatal ACOX1 deficiencyAdrenoleukodystrophy X linkedAdrenoleukodystrophyAdrenomyeloneuropathy
ALDH3A2 Aldehyde dehydrogenase3A2alpha OxidationAMACRAMP activated protein kinaseATFB ETF electron transfer flavoproteinBAATbeta oxidationCarnitine shuttleCAT CatalaseCholic acidCPT1 Carnitine palmitoyltransferaseCPT1aCPT1bCPT2 Carnitine plamitoyl transferase2CRAT Carnitine acetyltransferaseCROT Carnitine O octanoyltransferaseD bifunctional protein deficiency MFP2 deficiency SCPx deficiencyDCI Dodecenoly CoA delta isomerase 3 2 trans enoyl CoA isomeraseDECR1 2 4 dienoyl CoA reductase1DECR2 2 4 Dienoyl CoA reductase 2 peroxisomalDHRS4 Dehydrogenase reductase SDR family 4DNML1ECH1 Enoyl CoA hydratase 1 peroxisomalECHS1 Ctotonase Enoyl CoA hydrataseEHHADH Enoyl CoA hydratase 3 hydroxyacyl CoA dehydrogenaseETFA ETF electron transfer flavoproteinETFDH ETF dehydrogenaseFABP1 L FABPFABP3
FAR1 Fatty acyl CoA reductase1FAR2 Fatty acyl CoA reductase2Fatty acids (oxidation)Glutaric aciduria type IIGOT2 Aspartate aminotransferase FABPpmHACL1 2 Hydroxyacyl CoA lyase 1HADH MSCHAD medium and short chain hydoxyacyl CoA dehydrogenaseHADHA HADHB MTP mitochondrial trifunctional proteinHAO2 Hydroxyacid oxidase 2 long chainHSD17B4HSDL2 Hydroxysteroid dehydrogenase like2Hypercholanemia familialIchthyosis prematurity syndrome FATP4 deficiency ACSVL5 deficiencyIDH1 Isocitrate dehydrogenase1 NADP solubleMFP1NUDT12 Nudix type motif12NUDT7 Nudix type motif 7OMIM p603850PDK pyruvate dehydrogenase kinasePECI Peroxisomal d3 d2 enoyl CoA isomerasePeroxisomesPEX1PEX10PEX12PEX13PEX14PEX16PEX19PEX2
PEX26PEX3PEX5PEX6PHYHPhytanic acidPrimary carnitine deficiencyPristanic acidPTS1PTS2Pyruvate dehydrogenase phosphatasePyruvate dehydrogenaseRacemase deficiencyRefsum s diseaseRhizomelic chondrodysplasia punctataSCP2SLC22A5 OCTN2 organic cation transporter2 CarnitineSLC25A2 CACT Carnitine acylcarnitine translocaseSLC27A1 FATP1SLC27A2SLC27A4 FATP4SLC27A5 FATP5SLC27A6 FATP6TYSND1Zellweger s syndrome
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