| Reactome:R-RNO-9711123 |
Cellular response to chemical stress |
| Reactome:R-SSC-9711123 |
Cellular response to chemical stress |
| Reactome:R-BTA-9711123 |
Cellular response to chemical stress |
| Reactome:R-MMU-9711123 |
Cellular response to chemical stress |
| Reactome:R-HSA-9711123 |
Cellular response to chemical stress |
| Reactome:R-BTA-8953897 |
Cellular responses to stimuli |
| Reactome:R-BTA-2262752 |
Cellular responses to stress |
| Reactome:R-MMU-3299685 |
Detoxification of Reactive Oxygen Species |
| Reactome:R-SSC-8953897 |
Cellular responses to stimuli |
| Reactome:R-SSC-2262752 |
Cellular responses to stress |
| Reactome:R-HSA-2262752 |
Cellular responses to stress |
| Reactome:R-RNO-8953897 |
Cellular responses to stimuli |
| Reactome:R-RNO-2262752 |
Cellular responses to stress |
| Reactome:R-HSA-3299685 |
Detoxification of Reactive Oxygen Species |
| Reactome:R-RNO-3299685 |
Detoxification of Reactive Oxygen Species |
| Reactome:R-BTA-3299685 |
Detoxification of Reactive Oxygen Species |
| Reactome:R-HSA-8953897 |
Cellular responses to stimuli |
| Reactome:R-MMU-8953897 |
Cellular responses to stimuli |
| Reactome:R-MMU-2262752 |
Cellular responses to stress |
| Reactome:R-SSC-3299685 |
Detoxification of Reactive Oxygen Species |
| PathBank:SMP0120670 |
Adenylosuccinate Lyase Deficiency |
| PathBank:SMP0000167 |
Adenylosuccinate Lyase Deficiency |
| PathBank:SMP0000220 |
Xanthine Dehydrogenase Deficiency (Xanthinuria) |
| PathBank:SMP0000512 |
Xanthinuria Type I |
| PathBank:SMP0000536 |
Mitochondrial DNA Depletion Syndrome-3 |
| PathBank:SMP0120669 |
Adenosine Deaminase Deficiency |
| PathBank:SMP0120673 |
AICA-Ribosiduria |
| PathBank:SMP0120709 |
Gout or Kelley-Seegmiller Syndrome |
| PathBank:SMP0120717 |
Xanthine Dehydrogenase Deficiency (Xanthinuria) |
| PathBank:SMP0120797 |
Xanthinuria Type II |
| PathBank:SMP0120821 |
Myoadenylate Deaminase Deficiency |
| PathBank:SMP0000050 |
Purine Metabolism |
| PathBank:SMP0000144 |
Adenosine Deaminase Deficiency |
| PathBank:SMP0000203 |
Molybdenum Cofactor Deficiency |
| PathBank:SMP0000428 |
Mercaptopurine Action Pathway |
| PathBank:SMP0000535 |
Adenine Phosphoribosyltransferase Deficiency (APRT) |
| PathBank:SMP0120728 |
Lesch-Nyhan Syndrome (LNS) |
| PathBank:SMP0120752 |
Molybdenum Cofactor Deficiency |
| PathBank:SMP0120756 |
Purine Nucleoside Phosphorylase Deficiency |
| PathBank:SMP0120796 |
Xanthinuria Type I |
| PathBank:SMP0120820 |
Mitochondrial DNA Depletion Syndrome |
| PathBank:SMP0000365 |
Gout or Kelley-Seegmiller Syndrome |
| PathBank:SMP0000210 |
Purine Nucleoside Phosphorylase Deficiency |
| PathBank:SMP0000430 |
Thioguanine Action Pathway |
| PathBank:SMP0000513 |
Xanthinuria Type II |
| PathBank:SMP0000537 |
Myoadenylate Deaminase Deficiency |
| PathBank:SMP0087332 |
Purine Metabolism |
| PathBank:SMP0120819 |
Adenine Phosphoribosyltransferase Deficiency (APRT) |
| PathBank:SMP0000364 |
Lesch-Nyhan Syndrome (LNS) |
| PathBank:SMP0000168 |
AICA-Ribosiduria |
| PathBank:SMP0000427 |
Azathioprine Action Pathway |
| PathBank:SMP0087239 |
Purine Metabolism |