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*  List of MeSH codes (D08)
... glucose 1-dehydrogenase MeSH D08.811.682.047.150.300 --- glucosephosphate dehydrogenase MeSH D08.811.682.047.150.600 --- ... acyl-coa dehydrogenases MeSH D08.811.682.660.150.100 --- acyl-coa dehydrogenase MeSH D08.811.682.660.150.150 --- acyl-coa ... l-iditol 2-dehydrogenase MeSH D08.811.682.047.150.700.649 --- mannitol dehydrogenase MeSH D08.811.682.047.150.900 --- uridine ... 11-beta-hydroxysteroid dehydrogenase type 1 MeSH D08.811.682.047.436.174.600 --- 11-beta-hydroxysteroid dehydrogenase type 2 ...
*  List of MeSH codes (C18)
... glucosephosphate dehydrogenase deficiency MeSH C18.452.648.437 --- hyperbilirubinemia, hereditary MeSH C18.452.648.437.281 --- ... pyruvate dehydrogenase complex deficiency disease MeSH C18.452.648.240 --- cytochrome-c oxidase deficiency MeSH C18.452.648.390 ... pyruvate dehydrogenase complex deficiency disease MeSH C18.452.100.100.875 --- tyrosinemias MeSH C18.452.100.360 --- hepatic ... pyruvate dehydrogenase complex deficiency disease MeSH C18.452.648.151.825 --- sphingolipidoses MeSH C18.452.648.151.825.200 ...
*  List of MeSH codes (C16)
... glucosephosphate dehydrogenase deficiency MeSH C16.320.070.480.370 --- favism MeSH C16.320.070.490 --- hemoglobin c disease ... glucosephosphate dehydrogenase deficiency MeSH C16.320.565.437 --- hyperbilirubinemia, hereditary MeSH C16.320.565.437.281 --- ... pyruvate dehydrogenase complex deficiency disease MeSH C16.320.322.500.937 --- rett syndrome MeSH C16.320.322.562 --- muscular ... pyruvate dehydrogenase complex deficiency disease MeSH C16.320.400.525.937 --- rett syndrome MeSH C16.320.400.540 --- myotonia ...
*  List of MeSH codes (C15)
... glucosephosphate dehydrogenase deficiency MeSH C15.378.071.141.150.480.370 --- favism MeSH C15.378.071.141.150.490 --- ...
*  List of diseases (G)
... phosphate dehydrogenase deficiency Glucose-6-phosphate translocase deficiency Glucose-galactose malabsorption Glucosephosphate ... II Glutaryl-CoA dehydrogenase deficiency Glutathione synthetase deficiency Glyceraldehyde-3-phosphate dehydrogenase deficiency ...
*  Genetic studies on Arabs
Shalev, O; Leibowitz, G; Brok-Simoni, F (Jun 15, 1994). "[Glucose phosphate isomerase deficiency with congenital nonspherocytic ... Rosler, A (August 2006). "17 beta-hydroxysteroid dehydrogenase 3 deficiency in the Mediterranean population". Pediatric ... glucose-6-phosphate dehydrogenase deficiency, and fragile X syndrome (FXS), which is an inherited genetic condition with ... glucose-6-phosphate dehydrogenase deficiency, alpha-thalassemia, molecular characterization, recessive osteoperosis, ...
*  Glycolysis
Cofactors: Mg2+ G6P is then rearranged into fructose 6-phosphate (F6P) by glucose phosphate isomerase. Fructose can also enter ... Glyceraldehyde-3-phosphate dehydrogenase NAD++ Pi NADH + H+ NAD++ Pi NADH + H+ 2 × 1,3-Bisphosphoglycerate 2 × Phosphoglycerate ...
*  List of OMIM disorder codes
PC Pyruvate dehydrogenase deficiency; 312170; PDHA1 Pyruvate dehydrogenase E2 deficiency; 245348; DLAT Pyruvate dehydrogenase ... due to glucose phosphate isomerase deficiency; 613470; GPI Hemolytic uremic syndrome, atypical, susceptibility to, 1; 235400; ... SCARB2 Acyl-CoA dehydrogenase, long chain, deficiency of; 201460; ACADL Acyl-CoA dehydrogenase, medium chain, deficiency of; ... TMPRSS6 Isobutyryl-CoA dehydrogenase deficiency; 611283; ACAD8 Isovaleric acidemia; 243500; IVD IVIC syndrome; 147750; SALL4 ...