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:2047 | hepatitis D | |
DOID:0040085 | bacterial sepsis | |
DOID:0050387 | nonpapillary renal cell carcinoma | |
DOID:0050471 | Carney complex | |
DOID:0050589 | inflammatory bowel disease | |
DOID:0050590 | severe congenital neutropenia | |
DOID:0050782 | Zollinger-Ellison syndrome | |
DOID:0050830 | peripheral artery disease | |
DOID:0050865 | tongue squamous cell carcinoma | |
DOID:0060041 | autism spectrum disorder |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024