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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 |
|---|---|---|---|---|---|
| C0267809 | Cirrhosis, Cryptogenic | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0007785 | Cerebral Infarction | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0039730 | Thalassemia | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0376670 | Pancreatitis, Alcoholic | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0036631 | Seminoma | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0796663 | Childhood Testicular Germ Cell Tumor | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0281361 | Adenocarcinoma of pancreas | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C1306759 | Eosinophilic disorder | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0027708 | Nephroblastoma | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0162739 | HELLP Syndrome | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0346153 | Breast Cancer, Familial | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0040517 | Gilles de la Tourette syndrome | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0001857 | AIDS related complex | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0023470 | Myeloid Leukemia | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0011603 | Dermatitis | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0003969 | Ascorbic Acid Deficiency | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0007124 | Noninfiltrating Intraductal Carcinoma | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0021841 | Intestinal Neoplasms | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0026848 | Myopathy | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0032002 | Pituitary Diseases | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C3469521 | FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder) | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0024121 | Lung Neoplasms | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C1855739 | Indifference to Pain, Congenital, Autosomal Recessive | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0015230 | Exanthema | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0041696 | Unipolar Depression | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
