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 59626 - 59650 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0011991 Diarrhea CHGA 1113 chromogranin A P10645
C0027819 Neuroblastoma CHGA 1113 chromogranin A P10645
C0001418 Adenocarcinoma CHGA 1113 chromogranin A P10645
C1335302 Pancreatic Ductal Adenocarcinoma CHGA 1113 chromogranin A P10645
C0031099 Periodontitis CHGA 1113 chromogranin A P10645
C0006826 Malignant Neoplasms CHGA 1113 chromogranin A P10645
C0007097 Carcinoma CHGA 1113 chromogranin A P10645
C0024115 Lung diseases CHGA 1113 chromogranin A P10645
C0011849 Diabetes Mellitus CHGA 1113 chromogranin A P10645
C1332979 Childhood Lymphoma CHGA 1113 chromogranin A P10645
C1306459 Primary malignant neoplasm CHGA 1113 chromogranin A P10645
C0796074 MOHR-TRANEBJAERG SYNDROME CHGA 1113 chromogranin A P10645
C0403447 Chronic Kidney Insufficiency CHGA 1113 chromogranin A P10645
C0011847 Diabetes CHGA 1113 chromogranin A P10645
C0013595 Eczema CHGA 1113 chromogranin A P10645
C0020538 Hypertensive disease CHGA 1113 chromogranin A P10645
C0206667 Adrenal Cortical Adenoma CHGA 1113 chromogranin A P10645
C0022336 Creutzfeldt-Jakob disease CHGA 1113 chromogranin A P10645
C0678222 Breast Carcinoma CHGA 1113 chromogranin A P10645
C0014859 Esophageal Neoplasms CHGA 1113 chromogranin A P10645
C2882221 Acute pulmonary embolism CHGA 1113 chromogranin A P10645
C1956346 Coronary Artery Disease CHGA 1113 chromogranin A P10645
C0026769 Multiple Sclerosis CHGA 1113 chromogranin A P10645
C0018801 Heart failure CHGA 1113 chromogranin A P10645
C0009324 Ulcerative Colitis CHGA 1113 chromogranin A P10645

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: August 19, 2024