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 7101 - 7125 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0029400 Osteitis CALR 811 calreticulin P27797
C0018213 Graves Disease CALR 811 calreticulin P27797
C0151744 Myocardial Ischemia CALR 811 calreticulin P27797
C0085278 Antiphospholipid Syndrome CALR 811 calreticulin P27797
C0035854 Rosacea CALR 811 calreticulin P27797
C1861172 Venous Thromboembolism CALR 811 calreticulin P27797
C0025229 Melioidosis CALR 811 calreticulin P27797
C0006370 Bulimia CALR 811 calreticulin P27797
C0343641 Human papilloma virus infection CALR 811 calreticulin P27797
C0020541 Portal Hypertension CALR 811 calreticulin P27797
C0006267 Bronchiectasis CALR 811 calreticulin P27797
C0085096 Peripheral Vascular Diseases CALR 811 calreticulin P27797
C0524620 Metabolic Syndrome X CALR 811 calreticulin P27797
C0014118 Endocarditis CALR 811 calreticulin P27797
C0023434 Chronic Lymphocytic Leukemia CALR 811 calreticulin P27797
C0021390 Inflammatory Bowel Diseases CALR 811 calreticulin P27797
C0007194 Hypertrophic Cardiomyopathy CALR 811 calreticulin P27797
C0009319 Colitis CALR 811 calreticulin P27797
C0024117 Chronic Obstructive Airway Disease CALR 811 calreticulin P27797
C0019158 Hepatitis CALR 811 calreticulin P27797
C0020538 Hypertensive disease CALR 811 calreticulin P27797
C0221013 Mastocytosis, Systemic CALR 811 calreticulin P27797
C1845862 Creatine deficiency, X-linked CALR 811 calreticulin P27797
C0002736 Amyotrophic Lateral Sclerosis CALR 811 calreticulin P27797
C0023465 Acute monocytic leukemia CALR 811 calreticulin P27797

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Last updated: August 19, 2024