Pathway Name | Organism |
---|---|
APAP ADME | Homo sapiens |
Aspirin ADME | Homo sapiens |
Defective UGT1A1 causes hyperbilirubinemia | Homo sapiens |
Glucuronidation | Homo sapiens |
Heme degradation | Homo sapiens |
DO ID | Disease Name | Source |
---|---|---|
DOID:0110756 | type 1 diabetes mellitus 19 | |
DOID:0110757 | type 1 diabetes mellitus 20 | |
DOID:0110758 | type 1 diabetes mellitus 21 | |
DOID:0110759 | type 1 diabetes mellitus 22 | |
DOID:0110760 | type 1 diabetes mellitus 23 | |
DOID:0110761 | type 1 diabetes mellitus 24 | |
DOID:0110845 | xeroderma pigmentosum group D | |
DOID:0110892 | inflammatory bowel disease 1 | |
DOID:0111029 | hemochromatosis type 1 | |
DOID:0111414 | trichohepatoenteric syndrome |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024