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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 | PGD | 5226 | phosphogluconate dehydrogenase | P52209 |
| C0013080 | Down Syndrome | PGD | 5226 | phosphogluconate dehydrogenase | P52209 |
| C0042900 | Vitiligo | PGD | 5226 | phosphogluconate dehydrogenase | P52209 |
| C0014859 | Esophageal Neoplasms | PGD | 5226 | phosphogluconate dehydrogenase | P52209 |
| C0036631 | Seminoma | PGD | 5226 | phosphogluconate dehydrogenase | P52209 |
| C0004509 | Azoospermia | PGD | 5226 | phosphogluconate dehydrogenase | P52209 |
| C0344315 | Depressed mood | PGD | 5226 | phosphogluconate dehydrogenase | P52209 |
| C0011570 | Mental Depression | PGD | 5226 | phosphogluconate dehydrogenase | P52209 |
| C0085413 | Polycystic Kidney, Autosomal Dominant | PGD | 5226 | phosphogluconate dehydrogenase | P52209 |
| C0011581 | Depressive disorder | PGD | 5226 | phosphogluconate dehydrogenase | P52209 |
| C0678222 | Breast Carcinoma | PGD | 5226 | phosphogluconate dehydrogenase | P52209 |
| C0013595 | Eczema | PGD | 5226 | phosphogluconate dehydrogenase | P52209 |
| C2239176 | Liver carcinoma | PGD | 5226 | phosphogluconate dehydrogenase | P52209 |
| C0009402 | Colorectal Carcinoma | PGM5 | 5239 | phosphoglucomutase 5 | Q15124 |
| C0005695 | Bladder Neoplasm | PGM5 | 5239 | phosphoglucomutase 5 | Q15124 |
| C0279000 | Liver and Intrahepatic Biliary Tract Carcinoma | PGM5 | 5239 | phosphoglucomutase 5 | Q15124 |
| C0005684 | Malignant neoplasm of urinary bladder | PGM5 | 5239 | phosphoglucomutase 5 | Q15124 |
| C0345904 | Malignant neoplasm of liver | PGM5 | 5239 | phosphoglucomutase 5 | Q15124 |
| C0699885 | Carcinoma of bladder | PGM5 | 5239 | phosphoglucomutase 5 | Q15124 |
| C3887645 | Job Syndrome | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
| C0029422 | Osteochondrodysplasias | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
| C0021051 | Immunologic Deficiency Syndromes | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
| C0036572 | Seizures | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
| C0013595 | Eczema | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
| C0018784 | Sensorineural Hearing Loss (disorder) | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
