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 |
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C0018802 | Congestive heart failure | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0023891 | Liver Cirrhosis, Alcoholic | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C2609414 | Acute kidney injury | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0035309 | Retinal Diseases | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0027066 | Myoclonus | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0001627 | Congenital adrenal hyperplasia | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0019159 | Hepatitis A | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C3887461 | Head and Neck Carcinoma | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0010674 | Cystic Fibrosis | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0017154 | Gastritis, Atrophic | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0279626 | Squamous cell carcinoma of esophagus | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C1565662 | Acute Kidney Insufficiency | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0005684 | Malignant neoplasm of urinary bladder | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0038325 | Stevens-Johnson Syndrome | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0007785 | Cerebral Infarction | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0235974 | Pancreatic carcinoma | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0013295 | Duodenal Ulcer | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0008370 | Cholestasis | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0740858 | Substance abuse problem | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0003467 | Anxiety | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0013146 | Drug abuse | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0022658 | Kidney Diseases | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0007137 | Squamous cell carcinoma | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0699885 | Carcinoma of bladder | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0038644 | Sudden infant death syndrome | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
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Last updated: August 19, 2024