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Results 1 - 10 of 285 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Show all pathways known for 1.3.8.1Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.1acetyl-coa c-acyltransferase deficiency 9848022 Clinical and biochemical features of fatty acid oxidation disorders. causal interaction
unassigned
4
0
Show all pathways known for 1.3.8.1Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.1acetyl-coa c-acyltransferase deficiency 10626578 Newborn screening with tandem mass spectrometry: 12 months' experience in NSW Australia. causal interaction
unassigned
3
0
Show all pathways known for 1.3.8.1Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.1acetyl-coa c-acyltransferase deficiency 16598811 Evaluation of electrospray-tandem mass spectrometry for the detection of phenylketonuria and other rare disorders. causal interaction
diagnostic usage
unassigned
2
1
0
Show all pathways known for 1.3.8.1Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.1Acidosis 26045367 Reveal genes functionally associated with ACADS by a network study. causal interaction
unassigned
1
0
Show all pathways known for 1.3.8.1Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.1Acidosis, Lactic 10626578 Newborn screening with tandem mass spectrometry: 12 months' experience in NSW Australia. causal interaction
unassigned
3
0
Show all pathways known for 1.3.8.1Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.1Acidosis, Lactic 32143453 Inherited Metabolic Diseases and Cardiac Pathology in Adults: Diagnosis and Prevalence in a CardioMetabo Study. causal interaction
diagnostic usage
unassigned
3
3
0
Show all pathways known for 1.3.8.1Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.1acyl-coa dehydrogenase deficiency 2326316 Molecular cloning and nucleotide sequence of cDNAs encoding human short chain acyl-CoA dehydrogenase and study of the molecular basis of human short chain acyl-CoA dehydrogenase deficiency. diagnostic usage
ongoing research
unassigned
3
2
0
Show all pathways known for 1.3.8.1Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.1acyl-coa dehydrogenase deficiency 10490047 Mitochondrial fatty acid oxidation disorders and cyclic vomiting syndrome. causal interaction
therapeutic application
unassigned
4
1
0
Show all pathways known for 1.3.8.1Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.1acyl-coa dehydrogenase deficiency 12013984 [Short chain acyl-CoA dehydrogenase deficiency] causal interaction
unassigned
4
0
Show all pathways known for 1.3.8.1Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.1acyl-coa dehydrogenase deficiency 14568186 A comparison of in vitro acylcarnitine profiling methods for the diagnosis of classical and variant short chain acyl-CoA dehydrogenase deficiency. diagnostic usage
unassigned
2
0
Results 1 - 10 of 285 > >>