Any feedback?
Please rate this page
(search_result.php)
(0/150)

BRENDA support

Refine search

Search Disease/ Diagnostics

show results
Refine your search

Search term:

Results 1 - 10 of 25 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Show all pathways known for 1.3.8.5Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.5acyl-coa dehydrogenase deficiency 17883863 2-methylbutyryl-CoA dehydrogenase deficiency associated with autism and mental retardation: a case report. causal interaction
unassigned
4
0
Show all pathways known for 1.3.8.5Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.5acyl-coa dehydrogenase deficiency 23712021 Prevalence and mutation analysis of short/branched chain acyl-CoA dehydrogenase deficiency (SBCADD) detected on newborn screening in Wisconsin. causal interaction
unassigned
4
0
Show all pathways known for 1.3.8.5Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.5acyl-coa dehydrogenase deficiency 27727436 Acylglycine Analysis by Ultra-Performance Liquid Chromatography-Tandem Mass Spectrometry (UPLC-MS/MS). causal interaction
diagnostic usage
unassigned
3
4
0
Show all pathways known for 1.3.8.5Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.5acyl-coa dehydrogenase deficiency 31555323 Biochemical, Clinical, and Genetic Characteristics of Short/Branched Chain Acyl-CoA Dehydrogenase Deficiency in Chinese Patients by Newborn Screening. causal interaction
diagnostic usage
unassigned
4
4
0
Show all pathways known for 1.3.8.5Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.5Intellectual Disability 17883863 2-methylbutyryl-CoA dehydrogenase deficiency associated with autism and mental retardation: a case report. causal interaction
unassigned
4
0
Show all pathways known for 1.3.8.5Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.5Maple Syrup Urine Disease 21290185 Advances and challenges in the treatment of branched-chain amino/keto acid metabolic defects. causal interaction
unassigned
3
0
Show all pathways known for 1.3.8.5Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.5medium-chain acyl-coa dehydrogenase deficiency 27727436 Acylglycine Analysis by Ultra-Performance Liquid Chromatography-Tandem Mass Spectrometry (UPLC-MS/MS). causal interaction
diagnostic usage
unassigned
3
4
0
Show all pathways known for 1.3.8.5Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.5methylcrotonoyl-coa carboxylase deficiency 27727436 Acylglycine Analysis by Ultra-Performance Liquid Chromatography-Tandem Mass Spectrometry (UPLC-MS/MS). causal interaction
diagnostic usage
unassigned
3
4
0
Show all pathways known for 1.3.8.5Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.5Multiple Acyl Coenzyme A Dehydrogenase Deficiency 27727436 Acylglycine Analysis by Ultra-Performance Liquid Chromatography-Tandem Mass Spectrometry (UPLC-MS/MS). causal interaction
diagnostic usage
unassigned
3
4
0
Show all pathways known for 1.3.8.5Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.5Propionic Acidemia 21290185 Advances and challenges in the treatment of branched-chain amino/keto acid metabolic defects. causal interaction
unassigned
3
0
Results 1 - 10 of 25 > >>