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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 |
|---|---|---|---|---|---|
| C0003850 | Arteriosclerosis | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0376358 | Malignant neoplasm of prostate | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0026764 | Multiple Myeloma | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0740391 | Middle Cerebral Artery Occlusion | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0085580 | Essential Hypertension | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0038454 | Cerebrovascular accident | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0035410 | Rhabdomyolysis | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0018099 | Gout | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0038644 | Sudden infant death syndrome | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0004153 | Atherosclerosis | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0243026 | Sepsis | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0155626 | Acute myocardial infarction | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0270736 | Essential Tremor | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0040034 | Thrombocytopenia | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0003868 | Arthritis, Gouty | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C1306459 | Primary malignant neoplasm | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0027947 | Neutropenia | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0948008 | Ischemic stroke | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0004096 | Asthma | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0031117 | Peripheral Neuropathy | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C1458155 | Mammary Neoplasms | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C1961102 | Precursor Cell Lymphoblastic Leukemia Lymphoma | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0023453 | L2 Acute Lymphoblastic Leukemia | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0023452 | Childhood Acute Lymphoblastic Leukemia | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
