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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 ▲ |
|---|---|---|---|---|---|
| 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 |
| C1704321 | Nephrotic Syndrome, Minimal Change | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0024530 | Malaria | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0040136 | Thyroid Neoplasm | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0026850 | Muscular Dystrophy | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
| C0241005 | Creatine phosphokinase serum increased | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
| C3279947 | NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9 | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
| C1837396 | CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ie | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
| C0018916 | Hemangioma | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
| C0398625 | Protein C Deficiency | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
| C0013274 | Patent ductus arteriosus | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
| C4317224 | Congenital disorder of glycosylation type 1q | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
| C0025958 | Microcephaly | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
| C0699743 | Congenital muscular dystrophy (disorder) | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
| C0272375 | Antithrombin III Deficiency | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
| C0039446 | Telangiectasis | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
| C0006826 | Malignant Neoplasms | PFKFB2 | 5208 | 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2 | O60825 |
| C1621958 | Glioblastoma Multiforme | PFKFB2 | 5208 | 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2 | O60825 |
