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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name ▼ | UniProt ID |
---|---|---|---|---|---|
C0017638 | Glioma | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C3887461 | Head and Neck Carcinoma | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0153633 | Malignant neoplasm of brain | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0344315 | Depressed mood | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C3203102 | Idiopathic pulmonary arterial hypertension | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0038013 | Ankylosing spondylitis | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C1800706 | Idiopathic Pulmonary Fibrosis | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0278996 | Malignant Head and Neck Neoplasm | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0006118 | Brain Neoplasms | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0856761 | Budd-Chiari Syndrome | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0027947 | Neutropenia | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0013537 | Eclampsia | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0018799 | Heart Diseases | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0001430 | Adenoma | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C2609414 | Acute kidney injury | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0027765 | nervous system disorder | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0008370 | Cholestasis | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0028754 | Obesity | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0033141 | Cardiomyopathies, Primary | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0036529 | Myocardial Diseases, Secondary | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0042384 | Vasculitis | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0563625 | Agnosia for Pain | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0019829 | Hodgkin Disease | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0015230 | Exanthema | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0007131 | Non-Small Cell Lung Carcinoma | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
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Last updated: August 19, 2024