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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 ▲ |
|---|---|---|---|---|---|
| C0394006 | Dysequilibrium syndrome | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0035920 | Rubella | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0553723 | Squamous cell carcinoma of skin | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0086543 | Cataract | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0271979 | Thalassemia Intermedia | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0015625 | Fanconi Anemia | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0023532 | Leukoplakia, Oral | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0027765 | nervous system disorder | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0085580 | Essential Hypertension | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0017677 | Glossitis, Benign Migratory | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0023643 | Lichen disease | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0017152 | Gastritis | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C1319315 | Adenocarcinoma of large intestine | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0699889 | Malignant Female Reproductive System Neoplasm | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C3469186 | HEMOCHROMATOSIS, TYPE 1 | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0007107 | Malignant neoplasm of larynx | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C1096903 | Sialic Acid Storage Disease, Finnish Type (disorder) | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0392525 | Nephrolithiasis | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0007121 | Bronchogenic Carcinoma | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0032463 | Polycythemia Vera | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0153594 | Malignant neoplasm of testis | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0267963 | Exocrine pancreatic insufficiency | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0009319 | Colitis | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0751688 | Malignant Squamous Cell Neoplasm | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0235946 | Cerebral atrophy | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
