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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 |
|---|---|---|---|---|---|
| C0014859 | Esophageal Neoplasms | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0006826 | Malignant Neoplasms | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0040156 | Thyrotoxicosis | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0007820 | Cerebrovascular Disorders | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0009324 | Ulcerative Colitis | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0023530 | Leukopenia | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C1861172 | Venous Thromboembolism | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0022658 | Kidney Diseases | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0027707 | Nephritis, Interstitial | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0014518 | Toxic Epidermal Necrolysis | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0024121 | Lung Neoplasms | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0279626 | Squamous cell carcinoma of esophagus | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C1458155 | Mammary Neoplasms | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C1565662 | Acute Kidney Insufficiency | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0345904 | Malignant neoplasm of liver | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0546837 | Malignant neoplasm of esophagus | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C1868683 | B-CELL MALIGNANCY, LOW-GRADE | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0024305 | Lymphoma, Non-Hodgkin | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0002395 | Alzheimer's Disease | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0038454 | Cerebrovascular accident | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0024115 | Lung diseases | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0007222 | Cardiovascular Diseases | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0038325 | Stevens-Johnson Syndrome | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0241910 | Autoimmune Chronic Hepatitis | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0678222 | Breast Carcinoma | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
