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 7051 - 7075 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0023418 leukemia CALR 811 calreticulin P27797
C0085669 Acute leukemia CALR 811 calreticulin P27797
C0007103 Malignant neoplasm of endometrium CALR 811 calreticulin P27797
C0007134 Renal Cell Carcinoma CALR 811 calreticulin P27797
C0242006 Myelofibrosis due to another disorder CALR 811 calreticulin P27797
C0027819 Neuroblastoma CALR 811 calreticulin P27797
C0392514 Hereditary hemochromatosis CALR 811 calreticulin P27797
C0019154 Hepatic Vein Thrombosis CALR 811 calreticulin P27797
C0265673 Congenital kyphosis CALR 811 calreticulin P27797
C0205824 Liposarcoma, Dedifferentiated CALR 811 calreticulin P27797
C0856761 Budd-Chiari Syndrome CALR 811 calreticulin P27797
C0003811 Cardiac Arrhythmia CALR 811 calreticulin P27797
C0040147 Thyroiditis CALR 811 calreticulin P27797
C0037023 Sialadenitis CALR 811 calreticulin P27797
C0014060 Encephalitis, St. Louis CALR 811 calreticulin P27797
C0018995 Hemochromatosis CALR 811 calreticulin P27797
C0220597 Adult Hodgkin Lymphoma CALR 811 calreticulin P27797
C0023643 Lichen disease CALR 811 calreticulin P27797
C0007112 Adenocarcinoma of prostate CALR 811 calreticulin P27797
C0272362 Acquired von Willebrand's disease CALR 811 calreticulin P27797
C0010674 Cystic Fibrosis CALR 811 calreticulin P27797
C1956346 Coronary Artery Disease CALR 811 calreticulin P27797
C0026847 Spinal Muscular Atrophy CALR 811 calreticulin P27797
C0243026 Sepsis CALR 811 calreticulin P27797
C0035309 Retinal Diseases CALR 811 calreticulin P27797

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Last updated: August 19, 2024