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 16901 - 16925 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0018802 Congestive heart failure CHGA 1113 chromogranin A P10645
C1265996 Large cell neuroendocrine carcinoma CHGA 1113 chromogranin A P10645
C0009319 Colitis CHGA 1113 chromogranin A P10645
C0036341 Schizophrenia CHGA 1113 chromogranin A P10645
C3536893 Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor CHGA 1113 chromogranin A P10645
C0242363 Islet Cell Tumor CHGA 1113 chromogranin A P10645
C0007131 Non-Small Cell Lung Carcinoma CHGA 1113 chromogranin A P10645
C0600139 Prostate carcinoma CHGA 1113 chromogranin A P10645
C0206754 Neuroendocrine Tumors CHGA 1113 chromogranin A P10645
C0014132 Endocrine Gland Neoplasms CHGA 1113 chromogranin A P10645
C0238462 Medullary carcinoma of thyroid CHGA 1113 chromogranin A P10645
C0003467 Anxiety CHGA 1113 chromogranin A P10645
C0005684 Malignant neoplasm of urinary bladder CHGA 1113 chromogranin A P10645
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

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Last updated: August 19, 2024