EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
2.4.1.131 | Congenital 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 |
2.4.1.131 | Congenital, 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 |
2.4.1.131 | Intellectual Disability |
22213132 |
Improved diagnostics lead to identification of three new patients with congenital disorder of glycosylation-Ip. |
causal interaction unassigned |
2 0 |
2.4.1.131 | Lipoma |
21563233 |
Gene expression and single nucleotide polymorphism array analyses of spindle cell lipomas and conventional lipomas with 13q14 deletion. |
causal interaction unassigned |
4 0 |
2.4.1.131 | Liver Neoplasms |
34150040 |
Prognostic gene biomarker identification in liver cancer by data mining. |
diagnostic usage unassigned |
2 0 |
2.4.1.131 | Metabolic 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 |
2.4.1.131 | Seizures |
22213132 |
Improved diagnostics lead to identification of three new patients with congenital disorder of glycosylation-Ip. |
causal interaction unassigned |
2 0 |
2.4.1.131 | Strabismus |
22213132 |
Improved diagnostics lead to identification of three new patients with congenital disorder of glycosylation-Ip. |
causal interaction unassigned |
2 0 |