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Results 1 - 10 of 147 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Show all pathways known for 1.3.8.9Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.9acid phosphatase deficiency 20691590 Disorders of muscle lipid metabolism: diagnostic and therapeutic challenges. causal interaction
therapeutic application
unassigned
3
1
0
Show all pathways known for 1.3.8.9Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.9Acidosis, Lactic 25298636 Fatty Acid oxidation disorder with secondary mitochondrial energy production defect: a case report. causal interaction
unassigned
3
0
Show all pathways known for 1.3.8.9Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.9acyl-coa dehydrogenase deficiency 18846621 Gene symbol: ACADVL. Disease: Very long chain acyl-CoA dehydrogenase deficiency. causal interaction
ongoing research
therapeutic application
unassigned
4
2
1
0
Show all pathways known for 1.3.8.9Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.9acyl-coa dehydrogenase deficiency 20373143 Newborn screening for disorders of fatty-acid oxidation: experience and recommendations from an expert meeting. causal interaction
unassigned
4
0
Show all pathways known for 1.3.8.9Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.9acyl-coa dehydrogenase deficiency 24801231 Clinical features and mutations in seven Chinese patients with very long chain acyl-CoA dehydrogenase deficiency. causal interaction
diagnostic usage
unassigned
4
2
0
Show all pathways known for 1.3.8.9Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.9acyl-coa dehydrogenase deficiency 26182500 [Clinical features and ACADVL gene mutation spectrum analysis of 11 Chinese patients with very long chain acyl-CoA dehydrogenase deficiency]. causal interaction
diagnostic usage
ongoing research
unassigned
4
4
2
0
Show all pathways known for 1.3.8.9Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.9Arrhythmias, Cardiac 33597881 Electrophysiological Abnormalities in VLCAD Deficient hiPSC-Cardiomyocytes Do not Improve with Carnitine Supplementation. causal interaction
therapeutic application
unassigned
4
3
0
Show all pathways known for 1.3.8.9Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.9biotinidase deficiency 16398167 [The advisory report 'Neonatal screening' from the Health Council of The Netherlands] causal interaction
causal interaction
unassigned
unassigned
4
4
0
0
Show all pathways known for 1.3.8.9Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.9Carcinogenesis 20099975 Differential gene expression identified in Uigur women cervical squamous cell carcinoma by suppression subtractive hybridization. causal interaction
therapeutic application
unassigned
3
2
0
Show all pathways known for 1.3.8.9Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.9Carcinoma, Hepatocellular 8379945 Hormonal and substrate regulation of 3-thia fatty acid metabolism in Morris 7800 C1 hepatoma cells. unassigned 0
Results 1 - 10 of 147 > >>