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 46051 - 46075 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0007131 Non-Small Cell Lung Carcinoma SRGN 5552 serglycin P10124
C0010051 Coronary Aneurysm SRGN 5552 serglycin P10124
C0011991 Diarrhea SRGN 5552 serglycin P10124
C0007102 Malignant tumor of colon SRGN 5552 serglycin P10124
C0007097 Carcinoma SRGN 5552 serglycin P10124
C0279626 Squamous cell carcinoma of esophagus SRGN 5552 serglycin P10124
C0035220 Respiratory Distress Syndrome, Newborn SRGN 5552 serglycin P10124
C0011884 Diabetic Retinopathy SRGN 5552 serglycin P10124
C0242379 Malignant neoplasm of lung SRGN 5552 serglycin P10124
C0011860 Diabetes Mellitus, Non-Insulin-Dependent SRGN 5552 serglycin P10124
C0017638 Glioma SRGN 5552 serglycin P10124
C0152013 Adenocarcinoma of lung (disorder) SRGN 5552 serglycin P10124
C0026764 Multiple Myeloma SRGN 5552 serglycin P10124
C0019163 Hepatitis B SRGN 5552 serglycin P10124
C0010068 Coronary heart disease SRGN 5552 serglycin P10124
C0004936 Mental disorders SRGN 5552 serglycin P10124
C1956346 Coronary Artery Disease SRGN 5552 serglycin P10124
C0699790 Colon Carcinoma SRGN 5552 serglycin P10124
C0023487 Acute Promyelocytic Leukemia SRGN 5552 serglycin P10124
C1449720 Adolescent Gynecomastia SRGN 5552 serglycin P10124
C0018802 Congestive heart failure SRGN 5552 serglycin P10124
C0221056 Adult type dermatomyositis SRGN 5552 serglycin P10124
C0020538 Hypertensive disease SRGN 5552 serglycin P10124
C1449563 Cardiomyopathy, Familial Idiopathic SRGN 5552 serglycin P10124
C0006840 Candidiasis SRGN 5552 serglycin P10124

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Last updated: August 19, 2024