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 12026 - 12050 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C1332206 Adult Lymphoma CHGA 1113 chromogranin A P10645
C0848548 hypertensive nephropathy CHGA 1113 chromogranin A P10645
C0031511 Pheochromocytoma CHGA 1113 chromogranin A P10645
C1336878 Ureter Small Cell Carcinoma CHGA 1113 chromogranin A P10645
C0019562 Von Hippel-Lindau Syndrome CHGA 1113 chromogranin A P10645
C0279988 Childhood Angiosarcoma CHGA 1113 chromogranin A P10645
C0699791 Stomach Carcinoma CHGA 1113 chromogranin A P10645
C0007137 Squamous cell carcinoma CHGA 1113 chromogranin A P10645
C0033375 Prolactinoma CHGA 1113 chromogranin A P10645
C0028754 Obesity CHGA 1113 chromogranin A P10645
C0155733 Atherosclerosis of aorta CHGA 1113 chromogranin A P10645
C0524851 Neurodegenerative Disorders CHGA 1113 chromogranin A P10645
C0011860 Diabetes Mellitus, Non-Insulin-Dependent CHGA 1113 chromogranin A P10645
C0235974 Pancreatic carcinoma CHGA 1113 chromogranin A P10645
C0279674 Small cell carcinoma of the cervix CHGA 1113 chromogranin A P10645
C0004238 Atrial Fibrillation CHGA 1113 chromogranin A P10645
C0524620 Metabolic Syndrome X CHGA 1113 chromogranin A P10645
C0022104 Irritable Bowel Syndrome CHGA 1113 chromogranin A P10645
C0003850 Arteriosclerosis CHGA 1113 chromogranin A P10645
C0017154 Gastritis, Atrophic CHGA 1113 chromogranin A P10645
C0206686 Adrenocortical carcinoma CHGA 1113 chromogranin A P10645
C0007138 Carcinoma, Transitional Cell CHGA 1113 chromogranin A P10645
C0699790 Colon Carcinoma CHGA 1113 chromogranin A P10645
C0002965 Angina, Unstable CHGA 1113 chromogranin A P10645
C0262584 Carcinoma, Small Cell CHGA 1113 chromogranin A P10645

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Last updated: August 19, 2024