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 39551 - 39575 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0009402 Colorectal Carcinoma CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C0006826 Malignant Neoplasms CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C1458155 Mammary Neoplasms CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C0699790 Colon Carcinoma CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C0011195 Dejerine-Sottas Disease (disorder) CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C0023452 Childhood Acute Lymphoblastic Leukemia CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C0010346 Crohn Disease CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C0023267 Fibroid Tumor CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C0001627 Congenital adrenal hyperplasia CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C0015695 Fatty Liver CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C0400966 Non-alcoholic Fatty Liver Disease CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C0007097 Carcinoma CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C0023895 Liver diseases CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C0280324 Laryngeal Squamous Cell Carcinoma CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C0001175 Acquired Immunodeficiency Syndrome CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C0085762 Alcohol abuse CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C0033578 Prostatic Neoplasms CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C0342474 Lipoid congenital adrenal hyperplasia CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C0038644 Sudden infant death syndrome CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C0042769 Virus Diseases CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C0014175 Endometriosis CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C0041296 Tuberculosis CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C1565489 Renal Insufficiency CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C1853230 Aphakia, congenital primary CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477
C0027051 Myocardial Infarction CYP4F3 4051 cytochrome P450 family 4 subfamily F member 3 Q08477

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Last updated: August 19, 2024