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 40826 - 40850 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0017638 Glioma CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C3887461 Head and Neck Carcinoma CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0153633 Malignant neoplasm of brain CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0344315 Depressed mood CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C3203102 Idiopathic pulmonary arterial hypertension CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0038013 Ankylosing spondylitis CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C1800706 Idiopathic Pulmonary Fibrosis CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0278996 Malignant Head and Neck Neoplasm CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0006118 Brain Neoplasms CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0856761 Budd-Chiari Syndrome CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0027947 Neutropenia CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0013537 Eclampsia CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0018799 Heart Diseases CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0001430 Adenoma CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C2609414 Acute kidney injury CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0027765 nervous system disorder CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0008370 Cholestasis CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0028754 Obesity CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0033141 Cardiomyopathies, Primary CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0036529 Myocardial Diseases, Secondary CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0042384 Vasculitis CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0563625 Agnosia for Pain CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0019829 Hodgkin Disease CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0015230 Exanthema CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0007131 Non-Small Cell Lung Carcinoma 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