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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 |
|---|---|---|---|---|---|
| C0021390 | Inflammatory Bowel Diseases | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C0238463 | Papillary thyroid carcinoma | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C0678222 | Breast Carcinoma | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C0018784 | Sensorineural Hearing Loss (disorder) | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C3714636 | Pneumonitis | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C0040136 | Thyroid Neoplasm | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C0007115 | Malignant neoplasm of thyroid | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C0431664 | Unilateral Cryptorchidism | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C0009319 | Colitis | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C0003850 | Arteriosclerosis | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C0029408 | Degenerative polyarthritis | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C0010278 | Craniosynostosis | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C0149516 | Chronic sinusitis | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C0033578 | Prostatic Neoplasms | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C0009324 | Ulcerative Colitis | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C0334579 | Anaplastic astrocytoma | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C1306459 | Primary malignant neoplasm | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C0002395 | Alzheimer's Disease | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C0014458 | Eosinophilia, Tropical | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C0002986 | Fabry Disease | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C0025149 | Medulloblastoma | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C3875321 | Inflammatory dermatosis | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C0014457 | Eosinophilia | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C1384666 | hearing impairment | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C0006142 | Malignant neoplasm of breast | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
