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:10211 | cholelithiasis | |
DOID:11151 | cholecystolithiasis | |
DOID:1380 | endometrial cancer | |
DOID:1612 | breast cancer | |
DOID:2043 | hepatitis B | |
DOID:2394 | ovarian cancer | |
DOID:2739 | Gilbert syndrome | |
DOID:2741 | bilirubin metabolic disorder | |
DOID:3803 | Crigler-Najjar syndrome | |
DOID:3908 | lung non-small cell carcinoma |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: April 7, 2025