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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 ▼ |
|---|---|---|---|---|---|
| C1857276 | Trichohepatoenteric Syndrome | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
| C0004775 | Bartter Disease | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
| C0001925 | Albuminuria | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
| C0034013 | Precocious Puberty | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
| C0015934 | Fetal Growth Retardation | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
| C0085580 | Essential Hypertension | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
| C0678222 | Breast Carcinoma | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
| C0038454 | Cerebrovascular accident | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
| C0029456 | Osteoporosis | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
| C0018799 | Heart Diseases | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
| C0020621 | Hypokalemia | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
| C0032460 | Polycystic Ovary Syndrome | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
| C0206667 | Adrenal Cortical Adenoma | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
| C0013336 | Dwarfism | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
| C0342482 | X-linked Adrenal Hypoplasia | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
| C1306459 | Primary malignant neoplasm | FOLR1 | 2348 | folate receptor alpha | P15328 |
| C0175693 | Russell-Silver syndrome | FOLR1 | 2348 | folate receptor alpha | P15328 |
| C0027651 | Neoplasms | FOLR1 | 2348 | folate receptor alpha | P15328 |
| C2931822 | Nasopharyngeal carcinoma | FOLR1 | 2348 | folate receptor alpha | P15328 |
| C0684249 | Carcinoma of lung | FOLR1 | 2348 | folate receptor alpha | P15328 |
| C0025500 | Mesothelioma | FOLR1 | 2348 | folate receptor alpha | P15328 |
| C0345904 | Malignant neoplasm of liver | FOLR1 | 2348 | folate receptor alpha | P15328 |
| C1140680 | Malignant neoplasm of ovary | FOLR1 | 2348 | folate receptor alpha | P15328 |
| C4721610 | Carcinoma, Ovarian Epithelial | FOLR1 | 2348 | folate receptor alpha | P15328 |
| C0699790 | Colon Carcinoma | FOLR1 | 2348 | folate receptor alpha | P15328 |
