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 45801 - 45825 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0002736 Amyotrophic Lateral Sclerosis CHGA 1113 chromogranin A P10645
C0021390 Inflammatory Bowel Diseases CHGA 1113 chromogranin A P10645
C0700095 Central neuroblastoma CHGA 1113 chromogranin A P10645
C0033578 Prostatic Neoplasms CHGA 1113 chromogranin A P10645
C1857276 Trichohepatoenteric Syndrome CHGA 1113 chromogranin A P10645
C0400822 Colitis, Lymphocytic CHGA 1113 chromogranin A P10645
C0006142 Malignant neoplasm of breast CHGA 1113 chromogranin A P10645
C0007102 Malignant tumor of colon CHGA 1113 chromogranin A P10645
C0027719 Nephrosclerosis CHGA 1113 chromogranin A P10645
C0206695 Carcinoma, Neuroendocrine CHGA 1113 chromogranin A P10645
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

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Last updated: August 19, 2024