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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 |
|---|---|---|---|---|---|
| C0600139 | Prostate carcinoma | DHRS11 | 79154 | dehydrogenase/reductase 11 | Q6UWP2 |
| C0238395 | Male Pseudohermaphroditism | DHRS11 | 79154 | dehydrogenase/reductase 11 | Q6UWP2 |
| C2930619 | Sex Differentiation Disorders | DHRS11 | 79154 | dehydrogenase/reductase 11 | Q6UWP2 |
| C0476089 | Endometrial Carcinoma | DHRS11 | 79154 | dehydrogenase/reductase 11 | Q6UWP2 |
| C0024623 | Malignant neoplasm of stomach | DHRS11 | 79154 | dehydrogenase/reductase 11 | Q6UWP2 |
| C1306459 | Primary malignant neoplasm | DHRS11 | 79154 | dehydrogenase/reductase 11 | Q6UWP2 |
| C0848558 | Hypospadias | DHRS11 | 79154 | dehydrogenase/reductase 11 | Q6UWP2 |
| C0266362 | Ambiguous Genitalia | DHRS11 | 79154 | dehydrogenase/reductase 11 | Q6UWP2 |
| C0007103 | Malignant neoplasm of endometrium | DHRS11 | 79154 | dehydrogenase/reductase 11 | Q6UWP2 |
| C0282528 | Peroxisomal Disorders | DHRS11 | 79154 | dehydrogenase/reductase 11 | Q6UWP2 |
| C0032460 | Polycystic Ovary Syndrome | DHRS11 | 79154 | dehydrogenase/reductase 11 | Q6UWP2 |
| C0006826 | Malignant Neoplasms | DHRS11 | 79154 | dehydrogenase/reductase 11 | Q6UWP2 |
| C0031511 | Pheochromocytoma | DHRS11 | 79154 | dehydrogenase/reductase 11 | Q6UWP2 |
| C1134719 | Invasive Ductal Breast Carcinoma | DHRS11 | 79154 | dehydrogenase/reductase 11 | Q6UWP2 |
| C0030567 | Parkinson Disease | DHRS11 | 79154 | dehydrogenase/reductase 11 | Q6UWP2 |
| C0026769 | Multiple Sclerosis | DHRS11 | 79154 | dehydrogenase/reductase 11 | Q6UWP2 |
| C0699791 | Stomach Carcinoma | DHRS11 | 79154 | dehydrogenase/reductase 11 | Q6UWP2 |
| C1458155 | Mammary Neoplasms | DHRS11 | 79154 | dehydrogenase/reductase 11 | Q6UWP2 |
| C0020725 | Type II Mucolipidosis | GNPTAB | 79158 | N-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Q3T906 |
| C0033788 | Pseudo-Hurler Polydystrophy | GNPTAB | 79158 | N-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Q3T906 |
| C0878544 | Cardiomyopathies | GNPTAB | 79158 | N-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Q3T906 |
| C2673377 | MUCOLIPIDOSIS II ALPHA/BETA (disorder) | GNPTAB | 79158 | N-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Q3T906 |
| C0019270 | Hernia | GNPTAB | 79158 | N-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Q3T906 |
| C0085078 | Lysosomal Storage Diseases | GNPTAB | 79158 | N-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Q3T906 |
| C1306503 | Congenital exomphalos | GNPTAB | 79158 | N-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Q3T906 |
