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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 |
|---|---|---|---|---|---|
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | TYMP | 1890 | thymidine phosphorylase | P19971 |
| C0685938 | Malignant neoplasm of gastrointestinal tract | TYMP | 1890 | thymidine phosphorylase | P19971 |
| C0699885 | Carcinoma of bladder | TYMP | 1890 | thymidine phosphorylase | P19971 |
| C4048328 | cervical cancer | TYMP | 1890 | thymidine phosphorylase | P19971 |
| C0278878 | Adult Glioblastoma | TYMP | 1890 | thymidine phosphorylase | P19971 |
| C0162292 | External Ophthalmoplegia | TYMP | 1890 | thymidine phosphorylase | P19971 |
| C0023520 | Leukodystrophy | TYMP | 1890 | thymidine phosphorylase | P19971 |
| C2749864 | MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA) | TYMP | 1890 | thymidine phosphorylase | P19971 |
| C0007222 | Cardiovascular Diseases | TYMP | 1890 | thymidine phosphorylase | P19971 |
| C0271623 | Hypogonadotropic hypogonadism | TYMP | 1890 | thymidine phosphorylase | P19971 |
| C0031117 | Peripheral Neuropathy | TYMP | 1890 | thymidine phosphorylase | P19971 |
| C0238463 | Papillary thyroid carcinoma | TYMP | 1890 | thymidine phosphorylase | P19971 |
| C0030421 | Paraganglioma | TYMP | 1890 | thymidine phosphorylase | P19971 |
| C0025521 | Inborn Errors of Metabolism | TYMP | 1890 | thymidine phosphorylase | P19971 |
| C0677886 | Epithelial ovarian cancer | TYMP | 1890 | thymidine phosphorylase | P19971 |
| C0022650 | Kidney Calculi | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
| C2239176 | Liver carcinoma | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
| C0020501 | Primary Hyperoxaluria | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
| C0010691 | Cystinuria | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
| C0155877 | Allergic asthma | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
| C0034735 | Raynaud Phenomenon | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
| C0004153 | Atherosclerosis | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
| C0020071 | Hereditary Sensory Autonomic Neuropathy, Type 1 | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
| C0035078 | Kidney Failure | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
| C0162311 | Androgenetic Alopecia | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
