EC: 2.3.1.16
acetyl-CoA C-acyltransferase (acyl-CoA:acetyl-CoA C-acyltransferase)
Pathways
| pathway id | name |
|---|---|
| BioCyc:META_PWY-6863 | pyruvate fermentation to hexanol (engineered) |
| BioCyc:META_FAO-PWY | fatty acid β-oxidation I |
| BioCyc:META_PWY-7339 | 10-trans-heptadecenoyl-CoA degradation (MFE-dependent, yeast) |
| BioCyc:META_PWY-7338 | 10-trans-heptadecenoyl-CoA degradation (reductase-dependent, yeast) |
| BioCyc:ECO_FAO-PWY | fatty acid β-oxidation I |
| BioCyc:YEAST_PWY-7288 | fatty acid β-oxidation (peroxisome) |
| BioCyc:MTBH37RV_PWY-6946 | cholesterol degradation to androstenedione II (cholesterol dehydrogenase) |
| BioCyc:ECOO157_PWY-7003 | glycerol degradation to butanol |
| BioCyc:ECOO157_PWY-5177 | glutaryl-CoA degradation |
| BioCyc:ECOO157_PWY-5676 | acetyl-CoA fermentation to butyrate II |
| BioCyc:ECOO157_PWY-6590 | superpathway of Clostridium acetobutylicum acidogenic fermentation |
| BioCyc:MOUSE_PWY-5138 | fatty acid β-oxidation IV (unsaturated, even number) |
| BioCyc:MOUSE_PWY-6061 | bile acid biosynthesis, neutral pathway |
| BioCyc:BSUB_FAO-PWY | fatty acid β-oxidation I |
| BioCyc:ECOL316407_FAO-PWY | fatty acid β-oxidation I |
| BioCyc:META_PWY-7340 | 9-cis, 11-trans-octadecadienoyl-CoA degradation (isomerase-dependent, yeast) |
| BioCyc:META_PWY-7337 | 10-cis-heptadecenoyl-CoA degradation (yeast) |
| BioCyc:META_PWY-6946 | cholesterol degradation to androstenedione II (cholesterol dehydrogenase) |
| BioCyc:YEAST_PWY-7338 | 10-trans-heptadecenoyl-CoA degradation (reductase-dependent) |
| BioCyc:YEAST_PWY-7339 | 10-trans-heptadecenoyl-CoA degradation (MFE-dependent) |
| BioCyc:VCHO_FAO-PWY | fatty acid β-oxidation I |
| BioCyc:ECOO157_CENTFERM-PWY | pyruvate fermentation to butanoate |
| BioCyc:META_PWY1-3 | polyhydroxybutanoate biosynthesis |
| BioCyc:META_PWY-7216 | (R)- and (S)-3-hydroxybutanoate biosynthesis (engineered) |
| BioCyc:META_PWY-7218 | photosynthetic 3-hydroxybutanoate biosynthesis (engineered) |
| BioCyc:META_PWY-7948 | 4-oxopentanoate degradation |
| BioCyc:META_PWY-7288 | fatty acid β-oxidation (peroxisome, yeast) |
| BioCyc:META_PWY-735 | jasmonic acid biosynthesis |
| BioCyc:META_PWY-6944 | androstenedione degradation |
| BioCyc:YEAST_PWY-7337 | 10-cis-heptadecenoyl-CoA degradation |
| BioCyc:ARA_PWY-5136 | fatty acid β-oxidation II (peroxisome) |
| BioCyc:MTBH37RV_PWY-6947 | superpathway of cholesterol degradation II (cholesterol dehydrogenase) |
| BioCyc:MTBH37RV_PWY-6945 | cholesterol degradation to androstenedione I (cholesterol oxidase) |
| BioCyc:ECOO157_GLUDEG-II-PWY | glutamate degradation VII (to butanoate) |
| BioCyc:ECOL199310_ILEUDEG-PWY | isoleucine degradation I |
| BioCyc:ECOL199310_FAO-PWY | fatty acid β-oxidation I |
| BioCyc:HUMAN_FAO-PWY | fatty acid β-oxidation |
| BioCyc:HUMAN_PWY66-391 | fatty acid β-oxidation (peroxisome) |
| BioCyc:META_PWY-561 | superpathway of glyoxylate cycle and fatty acid degradation |
| BioCyc:META_PWY-5136 | fatty acid β-oxidation II (peroxisome) |
| BioCyc:META_PWY66-391 | fatty acid β-oxidation VI (peroxisome) |
| BioCyc:META_PWY-6947 | superpathway of cholesterol degradation II (cholesterol dehydrogenase) |
| BioCyc:META_PWY-6945 | cholesterol degradation to androstenedione I (cholesterol oxidase) |
| BioCyc:YEAST_YEAST-FAO-PWY | fatty acid oxidation (non-cyclic) |
| BioCyc:YEAST_PWY-7340 | 9-cis, 11-trans-octadecadienoyl-CoA degradation (isomerase-dependent) |
| BioCyc:MTBH37RV_PWY-6944 | androstenedione degradation |
| BioCyc:ECOO157_PWY-7401 | crotonate fermentation (to acetate and cyclohexane carboxylate) |
| BioCyc:ECOO157_ACETOACETATE-DEG-PWY | acetoacetate degradation (to acetyl CoA) |
| BioCyc:MOUSE_FAO-PWY | fatty acid β-oxidation I |
| BioCyc:MOUSE_PWY-2361 | 3-oxoadipate degradation |
| BioCyc:MOUSE_PWY-5136 | fatty acid β-oxidation II (core pathway) |
| WikiPathways:WP2472 | Escherichia coli K-12 peripherome |
| PathBank:SMP0000781 | Fatty Acid Oxidation |
| PathBank:SMP0001033 | fatty acid oxidation (Butanoate) |
| PathBank:SMP0001034 | fatty acid oxidation (Decanoate) |
| PathBank:SMP0001035 | fatty acid oxidation (hexanoate) |
| PathBank:SMP0001036 | Fatty Acid Oxidation (Laurate) |
| PathBank:SMP0001037 | fatty acid oxidation (myristate) |
| PathBank:SMP0001038 | fatty acid oxidation (octanoate) |
| PathBank:SMP0001039 | fatty acid oxidation (palmitate) |
| PathBank:SMP0001040 | fatty acid oxidation (steareate) |
| Reactome:R-BTA-1430728 | Metabolism |
| Reactome:R-BTA-556833 | Metabolism of lipids |
| Reactome:R-BTA-77286 | mitochondrial fatty acid beta-oxidation of saturated fatty acids |
| Reactome:R-BTA-77346 | Beta oxidation of decanoyl-CoA to octanoyl-CoA-CoA |
| Reactome:R-CEL-77286 | mitochondrial fatty acid beta-oxidation of saturated fatty acids |
| Reactome:R-CEL-77346 | Beta oxidation of decanoyl-CoA to octanoyl-CoA-CoA |
| Reactome:R-HSA-2046106 | alpha-linolenic acid (ALA) metabolism |
| Reactome:R-HSA-77286 | mitochondrial fatty acid beta-oxidation of saturated fatty acids |
| Reactome:R-HSA-77346 | Beta oxidation of decanoyl-CoA to octanoyl-CoA-CoA |
| Reactome:R-HSA-77288 | mitochondrial fatty acid beta-oxidation of unsaturated fatty acids |
| Reactome:R-HSA-9033500 | TYSND1 cleaves peroxisomal proteins |
| Reactome:R-MMU-1430728 | Metabolism |
| Reactome:R-MMU-556833 | Metabolism of lipids |
| Reactome:R-MMU-2046106 | alpha-linolenic acid (ALA) metabolism |
| Reactome:R-MMU-77286 | mitochondrial fatty acid beta-oxidation of saturated fatty acids |
| Reactome:R-MMU-77346 | Beta oxidation of decanoyl-CoA to octanoyl-CoA-CoA |
| Reactome:R-MMU-389887 | Beta-oxidation of pristanoyl-CoA |
| Reactome:R-MMU-8957322 | Metabolism of steroids |
| Reactome:R-RNO-8978868 | Fatty acid metabolism |
| Reactome:R-RNO-2046104 | alpha-linolenic (omega3) and linoleic (omega6) acid metabolism |
| Reactome:R-RNO-77289 | Mitochondrial Fatty Acid Beta-Oxidation |
| Reactome:R-RNO-77310 | Beta oxidation of lauroyl-CoA to decanoyl-CoA-CoA |
| Reactome:R-RNO-1482798 | Acyl chain remodeling of CL |
| Reactome:R-RNO-193368 | Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol |
| Reactome:R-SCE-2046106 | alpha-linolenic acid (ALA) metabolism |
| Reactome:R-BTA-8978868 | Fatty acid metabolism |
| Reactome:R-BTA-77289 | Mitochondrial Fatty Acid Beta-Oxidation |
| Reactome:R-BTA-77310 | Beta oxidation of lauroyl-CoA to decanoyl-CoA-CoA |
| Reactome:R-CEL-556833 | Metabolism of lipids |
| Reactome:R-CEL-77289 | Mitochondrial Fatty Acid Beta-Oxidation |
| Reactome:R-CEL-77310 | Beta oxidation of lauroyl-CoA to decanoyl-CoA-CoA |
| Reactome:R-HSA-556833 | Metabolism of lipids |
| Reactome:R-HSA-8978868 | Fatty acid metabolism |
| Reactome:R-HSA-2046104 | alpha-linolenic (omega3) and linoleic (omega6) acid metabolism |
| Reactome:R-HSA-77289 | Mitochondrial Fatty Acid Beta-Oxidation |
| Reactome:R-HSA-77310 | Beta oxidation of lauroyl-CoA to decanoyl-CoA-CoA |
| Reactome:R-HSA-1482798 | Acyl chain remodeling of CL |
| Reactome:R-HSA-9033241 | Peroxisomal protein import |
| Reactome:R-MMU-8978868 | Fatty acid metabolism |
| Reactome:R-MMU-2046104 | alpha-linolenic (omega3) and linoleic (omega6) acid metabolism |
| Reactome:R-MMU-77289 | Mitochondrial Fatty Acid Beta-Oxidation |
| Reactome:R-MMU-77310 | Beta oxidation of lauroyl-CoA to decanoyl-CoA-CoA |
| Reactome:R-MMU-1482798 | Acyl chain remodeling of CL |
| Reactome:R-MMU-193368 | Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol |
| Reactome:R-RNO-77285 | Beta oxidation of myristoyl-CoA to lauroyl-CoA |
| Reactome:R-RNO-77350 | Beta oxidation of hexanoyl-CoA to butanoyl-CoA |
| Reactome:R-RNO-390918 | Peroxisomal lipid metabolism |
| Reactome:R-RNO-1483206 | Glycerophospholipid biosynthesis |
| Reactome:R-RNO-192105 | Synthesis of bile acids and bile salts |
| Reactome:R-SCE-1430728 | Metabolism |
| Reactome:R-SCE-8978868 | Fatty acid metabolism |
| Reactome:R-SCE-2046104 | alpha-linolenic (omega3) and linoleic (omega6) acid metabolism |
| Reactome:R-SCE-390918 | Peroxisomal lipid metabolism |
| Reactome:R-BTA-77305 | Beta oxidation of palmitoyl-CoA to myristoyl-CoA |
| Reactome:R-BTA-77348 | Beta oxidation of octanoyl-CoA to hexanoyl-CoA |
| Reactome:R-BTA-1483257 | Phospholipid metabolism |
| Reactome:R-CEL-8978868 | Fatty acid metabolism |
| Reactome:R-CEL-77305 | Beta oxidation of palmitoyl-CoA to myristoyl-CoA |
| Reactome:R-CEL-77348 | Beta oxidation of octanoyl-CoA to hexanoyl-CoA |
| Reactome:R-CEL-1483257 | Phospholipid metabolism |
| Reactome:R-HSA-77305 | Beta oxidation of palmitoyl-CoA to myristoyl-CoA |
| Reactome:R-HSA-77348 | Beta oxidation of octanoyl-CoA to hexanoyl-CoA |
| Reactome:R-HSA-390247 | Beta-oxidation of very long chain fatty acids |
| Reactome:R-HSA-1483257 | Phospholipid metabolism |
| Reactome:R-HSA-9609507 | Protein localization |
| Reactome:R-MMU-77305 | Beta oxidation of palmitoyl-CoA to myristoyl-CoA |
| Reactome:R-MMU-77348 | Beta oxidation of octanoyl-CoA to hexanoyl-CoA |
| Reactome:R-MMU-390247 | Beta-oxidation of very long chain fatty acids |
| Reactome:R-MMU-1483257 | Phospholipid metabolism |
| Reactome:R-MMU-194068 | Bile acid and bile salt metabolism |
| Reactome:R-RNO-1430728 | Metabolism |
| Reactome:R-RNO-556833 | Metabolism of lipids |
| Reactome:R-RNO-2046106 | alpha-linolenic acid (ALA) metabolism |
| Reactome:R-RNO-77286 | mitochondrial fatty acid beta-oxidation of saturated fatty acids |
| Reactome:R-RNO-77346 | Beta oxidation of decanoyl-CoA to octanoyl-CoA-CoA |
| Reactome:R-RNO-389887 | Beta-oxidation of pristanoyl-CoA |
| Reactome:R-RNO-8957322 | Metabolism of steroids |
| Reactome:R-SCE-556833 | Metabolism of lipids |
| Reactome:R-BTA-77285 | Beta oxidation of myristoyl-CoA to lauroyl-CoA |
| Reactome:R-BTA-77350 | Beta oxidation of hexanoyl-CoA to butanoyl-CoA |
| Reactome:R-BTA-1483206 | Glycerophospholipid biosynthesis |
| Reactome:R-BTA-1482798 | Acyl chain remodeling of CL |
| Reactome:R-CEL-1430728 | Metabolism |
| Reactome:R-CEL-77285 | Beta oxidation of myristoyl-CoA to lauroyl-CoA |
| Reactome:R-CEL-77350 | Beta oxidation of hexanoyl-CoA to butanoyl-CoA |
| Reactome:R-CEL-1483206 | Glycerophospholipid biosynthesis |
| Reactome:R-CEL-1482798 | Acyl chain remodeling of CL |
| Reactome:R-HSA-1430728 | Metabolism |
| Reactome:R-HSA-77285 | Beta oxidation of myristoyl-CoA to lauroyl-CoA |
| Reactome:R-HSA-77350 | Beta oxidation of hexanoyl-CoA to butanoyl-CoA |
| Reactome:R-HSA-390918 | Peroxisomal lipid metabolism |
| Reactome:R-HSA-1483206 | Glycerophospholipid biosynthesis |
| Reactome:R-MMU-77285 | Beta oxidation of myristoyl-CoA to lauroyl-CoA |
| Reactome:R-MMU-77350 | Beta oxidation of hexanoyl-CoA to butanoyl-CoA |
| Reactome:R-MMU-390918 | Peroxisomal lipid metabolism |
| Reactome:R-MMU-1483206 | Glycerophospholipid biosynthesis |
| Reactome:R-MMU-192105 | Synthesis of bile acids and bile salts |
| Reactome:R-RNO-77305 | Beta oxidation of palmitoyl-CoA to myristoyl-CoA |
| Reactome:R-RNO-77348 | Beta oxidation of octanoyl-CoA to hexanoyl-CoA |
| Reactome:R-RNO-390247 | Beta-oxidation of very long chain fatty acids |
| Reactome:R-RNO-1483257 | Phospholipid metabolism |
| Reactome:R-RNO-194068 | Bile acid and bile salt metabolism |
| Reactome:R-SCE-390247 | Beta-oxidation of very long chain fatty acids |
| WikiPathways:WP5123 | Mitochondrial fatty acid oxidation disorders |
| WikiPathways:WP1941 | Peroxisomal beta-oxidation of tetracosanoyl-CoA |
| WikiPathways:WP2318 | Fatty acid oxidation |
| PathBank:SMP0120662 | 3-Methylcrotonyl-CoA Carboxylase Deficiency Type I |
| PathBank:SMP0120806 | 3-Hydroxyisobutyric Aciduria |
| PathBank:SMP0120822 | Carnitine Palmitoyl Transferase Deficiency I |
| PathBank:SMP0120826 | Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) |
| PathBank:SMP0120440 | 3-Hydroxy-3-methylglutaryl-CoA Lyase Deficiency |
| PathBank:SMP0120444 | 3-Methylglutaconic Aciduria Type IV |
| PathBank:SMP0120468 | Congenital Bile Acid Synthesis Defect Type III |
| PathBank:SMP0120516 | Maple Syrup Urine Disease |
| PathBank:SMP0120589 | Isovaleric Acidemia |
| PathBank:SMP0121348 | Fatty Acid Oxidation (Hexanoate) |
| PathBank:SMP0121352 | Fatty Acid Oxidation (Palmitate) |
| PathBank:SMP0000032 | Valine, Leucine, and Isoleucine Degradation |
| PathBank:SMP0000051 | Fatty Acid Metabolism |
| PathBank:SMP0000173 | beta-Ketothiolase Deficiency |
| PathBank:SMP0000199 | Maple Syrup Urine Disease |
| PathBank:SMP0000384 | Methylmalonate Semialdehyde Dehydrogenase Deficiency |
| PathBank:SMP0000235 | Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD Deficiency) |
| PathBank:SMP0000482 | Mitochondrial Beta-Oxidation of Long Chain Saturated Fatty Acids |
| PathBank:SMP0000318 | Congenital Bile Acid Synthesis Defect Type III |
| PathBank:SMP0000141 | 3-Methylglutaconic Aciduria Type IV |
| PathBank:SMP0000524 | Isovaleric Acidemia |
| PathBank:SMP0000540 | Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD) |
| PathBank:SMP0000544 | Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase Deficiency (LCHAD) |
| PathBank:SMP0000568 | Short-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (SCHAD) |
| PathBank:SMP0087294 | Fatty Acid Elongation in Mitochondria |
| PathBank:SMP0087358 | Mitochondrial Beta-Oxidation of Short Chain Saturated Fatty Acids |
| PathBank:SMP0087430 | Fatty Acid Metabolism |
| PathBank:SMP0120661 | 3-Hydroxy-3-methylglutaryl-CoA Lyase Deficiency |
| PathBank:SMP0120665 | 3-Methylglutaconic Aciduria Type IV |
| PathBank:SMP0120745 | Methylmalonic Aciduria |
| PathBank:SMP0120757 | Propionic Acidemia |
| PathBank:SMP0120805 | 3-Hydroxyisobutyric Acid Dehydrogenase Deficiency |
| PathBank:SMP0120825 | Carnitine Palmitoyl Transferase Deficiency II |
| PathBank:SMP0120439 | 2-Methyl-3-hydroxybutryl-CoA Dehydrogenase Deficiency |
| PathBank:SMP0120443 | 3-Methylglutaconic Aciduria Type III |
| PathBank:SMP0120459 | beta-Ketothiolase Deficiency |
| PathBank:SMP0120463 | Cerebrotendinous Xanthomatosis (CTX) |
| PathBank:SMP0120467 | Congenital Bile Acid Synthesis Defect Type II |
| PathBank:SMP0120495 | Zellweger Syndrome |
| PathBank:SMP0120503 | Isovaleric Aciduria |
| PathBank:SMP0120523 | Methylmalonate Semialdehyde Dehydrogenase Deficiency |
| PathBank:SMP0120588 | Isobutyryl-CoA Dehydrogenase Deficiency |
| PathBank:SMP0120632 | Short-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (SCHAD) |
| PathBank:SMP0121206 | Jasmonic Acid Biosynthesis |
| PathBank:SMP0121347 | Fatty Acid Oxidation (Decanoate) |
| PathBank:SMP0121351 | Fatty Acid Oxidation (Octanoate) |
| PathBank:SMP0000054 | Fatty Acid Elongation in Mitochondria |
| PathBank:SMP0000035 | Bile Acid Biosynthesis |
| PathBank:SMP0000138 | 3-Hydroxy-3-methylglutaryl-CoA Lyase Deficiency |
| PathBank:SMP0000140 | 3-Methylglutaconic Aciduria Type III |
| PathBank:SMP0000238 | Isovaleric Aciduria |
| PathBank:SMP0000185 | Glutaric Aciduria Type I |
| PathBank:SMP0000481 | Mitochondrial Beta-Oxidation of Medium Chain Saturated Fatty Acids |
| PathBank:SMP0000314 | Congenital Bile Acid Synthesis Defect Type II |
| PathBank:SMP0000315 | Cerebrotendinous Xanthomatosis (CTX) |
| PathBank:SMP0000523 | Isobutyryl-CoA Dehydrogenase Deficiency |
| PathBank:SMP0000539 | Long Chain Acyl-CoA Dehydrogenase Deficiency (LCAD) |
| PathBank:SMP0002361 | Fatty Acid Metabolism |
| PathBank:SMP0002368 | Fatty Acid Elongation In Mitochondria |
| PathBank:SMP0002381 | Steroid Biosynthesis |
| PathBank:SMP0087521 | Mitochondrial Beta-Oxidation of Medium Chain Saturated Fatty Acids |
| PathBank:SMP0063641 | Mitochondrial Beta-Oxidation of Short Chain Saturated Fatty Acids |
| PathBank:SMP0063689 | Valine, Leucine, and Isoleucine Degradation |
| PathBank:SMP0120652 | 27-Hydroxylase Deficiency |
| PathBank:SMP0120660 | 2-Methyl-3-hydroxybutryl-CoA Dehydrogenase Deficiency |
| PathBank:SMP0120664 | 3-Methylglutaconic Aciduria Type III |
| PathBank:SMP0120696 | Ethylmalonic Encephalopathy |
| PathBank:SMP0120736 | Maple Syrup Urine Disease |
| PathBank:SMP0120740 | Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD Deficiency) |
| PathBank:SMP0120808 | Isovaleric Acidemia |
| PathBank:SMP0120824 | Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD) |
| PathBank:SMP0120828 | Trifunctional Protein Deficiency |
| PathBank:SMP0120441 | 3-Methylcrotonyl-CoA Carboxylase Deficiency Type I |
| PathBank:SMP0120477 | Familial Hypercholanemia (FHCA) |
| PathBank:SMP0120525 | Methylmalonic Aciduria |
| PathBank:SMP0120537 | Propionic Acidemia |
| PathBank:SMP0120586 | 3-Hydroxyisobutyric Acid Dehydrogenase Deficiency |
| PathBank:SMP0121261 | Fatty Acid Oxidation |
| PathBank:SMP0121349 | Fatty Acid Oxidation (Laurate) |
| PathBank:SMP0121353 | Fatty Acid Oxidation (Steareate) |
| PathBank:SMP0000137 | 2-Methyl-3-hydroxybutyryl-CoA Dehydrogenase Deficiency |
| PathBank:SMP0000237 | 3-Methylcrotonyl-CoA Carboxylase Deficiency Type I |
| PathBank:SMP0000200 | Methylmalonic Aciduria |
| PathBank:SMP0000317 | Familial Hypercholanemia (FHCA) |
| PathBank:SMP0000521 | 3-Hydroxyisobutyric Acid Dehydrogenase Deficiency |
| PathBank:SMP0000541 | Carnitine Palmitoyl Transferase Deficiency II |
| PathBank:SMP0000545 | Trifunctional Protein Deficiency |
| PathBank:SMP0002383 | Ketone Body Metabolism |
| PathBank:SMP0087280 | Fatty Acid Metabolism |
| PathBank:SMP0087360 | Mitochondrial Beta-Oxidation of Long Chain Saturated Fatty Acids |
| PathBank:SMP0012062 | Fatty Acid Beta-Oxidation I |
| PathBank:SMP0063640 | Mitochondrial Beta-Oxidation of Medium Chain Saturated Fatty Acids |
| PathBank:SMP0120663 | 3-Methylglutaconic Aciduria Type I |
| PathBank:SMP0120679 | beta-Ketothiolase Deficiency |
| PathBank:SMP0120723 | Isovaleric Aciduria |
| PathBank:SMP0120743 | Methylmalonate Semialdehyde Dehydrogenase Deficiency |
| PathBank:SMP0120807 | Isobutyryl-CoA Dehydrogenase Deficiency |
| PathBank:SMP0120823 | Long Chain Acyl-CoA Dehydrogenase Deficiency (LCAD) |
| PathBank:SMP0120827 | Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase Deficiency (LCHAD) |
| PathBank:SMP0120851 | Short-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (SCHAD) |
| PathBank:SMP0120442 | 3-Methylglutaconic Aciduria Type I |
| PathBank:SMP0120587 | 3-Hydroxyisobutyric Aciduria |
| PathBank:SMP0121346 | Fatty Acid Oxidation (Butanoate) |
| PathBank:SMP0121350 | Fatty Acid Oxidation (Myristate) |
| PathBank:SMP0122254 | Acetate Metabolism |
| PathBank:SMP0000236 | Propionic Acidemia |
| PathBank:SMP0000139 | 3-Methylglutaconic Aciduria Type I |
| PathBank:SMP0000181 | Ethylmalonic Encephalopathy |
| PathBank:SMP0000480 | Mitochondrial Beta-Oxidation of Short Chain Saturated Fatty Acids |
| PathBank:SMP0000316 | Zellweger Syndrome |
| PathBank:SMP0000522 | 3-Hydroxyisobutyric Aciduria |
| PathBank:SMP0000538 | Carnitine Palmitoyl Transferase Deficiency I |
| PathBank:SMP0000542 | Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) |
| PathBank:SMP0000635 | Valproic Acid Metabolism Pathway |
| PathBank:SMP0000720 | 27-Hydroxylase Deficiency |
| PathBank:SMP0002384 | Terpenoid Backbone Biosynthesis |
| PathBank:SMP0087327 | Valine, Leucine, and Isoleucine Degradation |
| PathBank:SMP0087359 | Mitochondrial Beta-Oxidation of Medium Chain Saturated Fatty Acids |
| PathBank:SMP0087523 | Mitochondrial Beta-Oxidation of Long Chain Saturated Fatty Acids |
| PathBank:SMP0063601 | Bile Acid Biosynthesis |
| PathBank:SMP0063639 | Mitochondrial Beta-Oxidation of Long Chain Saturated Fatty Acids |