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 16876 - 16900 of 62743 in total
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