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DisGeNET
DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
| Source | Last Updated |
|---|---|
| DisGeNET | July 29, 2024 |
| Disease ID | Disease Name | Gene Symbol ▲ | Gene ID | Gene Name | UniProt ID |
|---|---|---|---|---|---|
| C0002875 | Cooley's anemia | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0027651 | Neoplasms | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0013336 | Dwarfism | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0015934 | Fetal Growth Retardation | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0011991 | Diarrhea | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C1704436 | Peripheral Arterial Diseases | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0678222 | Breast Carcinoma | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0345904 | Malignant neoplasm of liver | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0006142 | Malignant neoplasm of breast | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0242379 | Malignant neoplasm of lung | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0023903 | Liver neoplasms | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0029182 | orbit (eye disorders) | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0345905 | Intrahepatic Cholangiocarcinoma | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0020501 | Primary Hyperoxaluria | UGDH | 7358 | UDP-glucose 6-dehydrogenase | O60701 |
| C0006826 | Malignant Neoplasms | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
| C0019196 | Hepatitis C | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
| C0600139 | Prostate carcinoma | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
| C0947622 | Cholecystolithiasis | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
| C0221757 | alpha 1-Antitrypsin Deficiency | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
| C0036572 | Seizures | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
| C0017551 | Gilbert Disease (disorder) | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
| C0002895 | Anemia, Sickle Cell | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
| C0271979 | Thalassemia Intermedia | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
| C0008350 | Cholelithiasis | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
| C0023895 | Liver diseases | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
