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 59151 - 59175 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C0019572 Hirsutism SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C1332206 Adult Lymphoma SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C1720830 Painful Bladder Syndrome SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0007097 Carcinoma SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0266929 Chronic Periodontitis SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0015934 Fetal Growth Retardation SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0027092 Myopia SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0021841 Intestinal Neoplasms SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0018817 Atrial Septal Defects SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0158761 Radioulnar Synostosis SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0038379 Strabismus SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0023466 Leukemia, Monocytic, Chronic SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0684249 Carcinoma of lung SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C1301937 Talipes SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0017168 Gastroesophageal reflux disease SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0017601 Glaucoma SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0025362 Mental Retardation SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0008925 Cleft Palate SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C4551851 Cornelia de Lange Syndrome 1 SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0006413 Burkitt Lymphoma SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C2239176 Liver carcinoma SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0000768 Congenital Abnormality SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0086543 Cataract SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0036857 Severe intellectual disability SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0023467 Leukemia, Myelocytic, Acute SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7

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Last updated: August 19, 2024