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Results 1 - 10 of 235 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Show all pathways known for 1.5.5.1Display the word mapDisplay the reaction diagram Show all sequences 1.5.5.1Acidosis 8617498 Assignment of Etfdh, Etfb, and Etfa to chromosomes 3, 7, and 13: the mouse homologs of genes responsible for glutaric acidemia type II in human. causal interaction
ongoing research
therapeutic application
unassigned
4
1
1
0
Show all pathways known for 1.5.5.1Display the word mapDisplay the reaction diagram Show all sequences 1.5.5.1Acidosis 17912479 Cardiomyopathy in multiple Acyl-CoA dehydrogenase deficiency: a clinico-pathological correlation and review of literature. causal interaction
therapeutic application
unassigned
2
1
0
Show all pathways known for 1.5.5.1Display the word mapDisplay the reaction diagram Show all sequences 1.5.5.1Acidosis 17977044 Risk of sudden death and acute life-threatening events in patients with glutaric acidemia type II. unassigned 0
Show all pathways known for 1.5.5.1Display the word mapDisplay the reaction diagram Show all sequences 1.5.5.1acyl-coa dehydrogenase deficiency 7360517 Multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II) with transient hypersarcosinemia and sarcosinuria; possible inherited deficiency of an electron transfer flavoprotein. causal interaction
unassigned
3
0
Show all pathways known for 1.5.5.1Display the word mapDisplay the reaction diagram Show all sequences 1.5.5.1acyl-coa dehydrogenase deficiency 9889013 Isolated isobutyryl-CoA dehydrogenase deficiency: an unrecognized defect in human valine metabolism. causal interaction
diagnostic usage
unassigned
1
3
0
Show all pathways known for 1.5.5.1Display the word mapDisplay the reaction diagram Show all sequences 1.5.5.1acyl-coa dehydrogenase deficiency 16165386 Identification of the human mitochondrial FAD transporter and its potential role in multiple acyl-CoA dehydrogenase deficiency. causal interaction
ongoing research
unassigned
2
2
0
Show all pathways known for 1.5.5.1Display the word mapDisplay the reaction diagram Show all sequences 1.5.5.1acyl-coa dehydrogenase deficiency 16510302 Electron transfer flavoprotein deficiency: functional and molecular aspects. causal interaction
diagnostic usage
therapeutic application
unassigned
4
2
1
0
Show all pathways known for 1.5.5.1Display the word mapDisplay the reaction diagram Show all sequences 1.5.5.1acyl-coa dehydrogenase deficiency 17050691 Structure of electron transfer flavoprotein-ubiquinone oxidoreductase and electron transfer to the mitochondrial ubiquinone pool. causal interaction
ongoing research
unassigned
1
2
0
Show all pathways known for 1.5.5.1Display the word mapDisplay the reaction diagram Show all sequences 1.5.5.1acyl-coa dehydrogenase deficiency 17912479 Cardiomyopathy in multiple Acyl-CoA dehydrogenase deficiency: a clinico-pathological correlation and review of literature. causal interaction
therapeutic application
unassigned
2
1
0
Show all pathways known for 1.5.5.1Display the word mapDisplay the reaction diagram Show all sequences 1.5.5.1acyl-coa dehydrogenase deficiency 19249206 ETFDH mutations, CoQ10 levels, and respiratory chain activities in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency. causal interaction
diagnostic usage
unassigned
2
2
0
Results 1 - 10 of 235 > >>