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 40726 - 40750 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C1306459 Primary malignant neoplasm CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0017567 Gingival Hypertrophy CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0009402 Colorectal Carcinoma CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0027051 Myocardial Infarction CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0023895 Liver diseases CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0011570 Mental Depression CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0750974 Brain Tumor, Primary CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0011860 Diabetes Mellitus, Non-Insulin-Dependent CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C2239176 Liver carcinoma CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0035309 Retinal Diseases CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0019154 Hepatic Vein Thrombosis CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0038644 Sudden infant death syndrome CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0011849 Diabetes Mellitus CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0014544 Epilepsy CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0041696 Unipolar Depression CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0004238 Atrial Fibrillation CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0026769 Multiple Sclerosis CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0003850 Arteriosclerosis CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C1269683 Major Depressive Disorder CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0017152 Gastritis CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C4721555 Autoimmune hepatitis CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0004943 Behcet Syndrome CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0152018 Esophageal carcinoma CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0030567 Parkinson Disease CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0751956 Acute Cerebrovascular Accidents CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024