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Results 1 - 8 of 8
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Show all pathways known for 2.4.1.131Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.131Congenital Disorders of Glycosylation 20080937 A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip. causal interaction
unassigned
4
0
Show all pathways known for 2.4.1.131Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.131Congenital, Hereditary, and Neonatal Diseases and Abnormalities 20080937 A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip. causal interaction
unassigned
4
0
Show all pathways known for 2.4.1.131Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.131Intellectual Disability 22213132 Improved diagnostics lead to identification of three new patients with congenital disorder of glycosylation-Ip. causal interaction
unassigned
2
0
Show all pathways known for 2.4.1.131Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.131Lipoma 21563233 Gene expression and single nucleotide polymorphism array analyses of spindle cell lipomas and conventional lipomas with 13q14 deletion. causal interaction
unassigned
4
0
Show all pathways known for 2.4.1.131Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.131Liver Neoplasms 34150040 Prognostic gene biomarker identification in liver cancer by data mining. diagnostic usage
unassigned
2
0
Show all pathways known for 2.4.1.131Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.131Metabolic Diseases 20080937 A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip. causal interaction
unassigned
4
0
Show all pathways known for 2.4.1.131Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.131Seizures 22213132 Improved diagnostics lead to identification of three new patients with congenital disorder of glycosylation-Ip. causal interaction
unassigned
2
0
Show all pathways known for 2.4.1.131Display the word mapDisplay the reaction diagram Show all sequences 2.4.1.131Strabismus 22213132 Improved diagnostics lead to identification of three new patients with congenital disorder of glycosylation-Ip. causal interaction
unassigned
2
0
Results 1 - 8 of 8