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 |
---|---|---|---|---|---|
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 |
C0031350 | Pharyngitis | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0024620 | Primary Malignant Liver Neoplasm | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0023465 | Acute monocytic leukemia | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0750952 | Biliary Tract Cancer | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0001080 | Achondroplasia | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0024121 | Lung Neoplasms | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0595989 | Carcinoma of larynx | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0024143 | Lupus Nephritis | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C3494522 | Hypergonadotropic Ovarian Failure, X-Linked | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0033578 | Prostatic Neoplasms | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C1862382 | SVEINSSON CHORIORETINAL ATROPHY | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
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Last updated: August 19, 2024