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
Displaying entries 16801 - 16825 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0027720 Nephrosis CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0009402 Colorectal Carcinoma CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0004096 Asthma CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0027651 Neoplasms CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0017152 Gastritis CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0376545 Hematologic Neoplasms CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0235480 Paroxysmal atrial fibrillation CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0004936 Mental disorders CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0004030 Aspergillosis CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0020538 Hypertensive disease CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0020473 Hyperlipidemia CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0751075 Cancer of Digestive System CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0036572 Seizures CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0038356 Stomach Neoplasms CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C1565489 Renal Insufficiency CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0026769 Multiple Sclerosis CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0007131 Non-Small Cell Lung Carcinoma CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0011860 Diabetes Mellitus, Non-Insulin-Dependent CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0242383 Age related macular degeneration CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0014742 Erythema Multiforme CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0041696 Unipolar Depression CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0036341 Schizophrenia CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0085580 Essential Hypertension CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0878544 Cardiomyopathies CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0007222 Cardiovascular Diseases CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261

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Last updated: August 19, 2024