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 61201 - 61225 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0376358 Malignant neoplasm of prostate UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0010414 Infection by Cryptococcus neoformans UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0005283 beta Thalassemia UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0027651 Neoplasms UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0600139 Prostate carcinoma UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0524620 Metabolic Syndrome X UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0017205 Gaucher Disease UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0268138 Xeroderma Pigmentosum, Complementation Group D UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0006826 Malignant Neoplasms UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0342751 Generalized glycogen storage disease of infants UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0028754 Obesity UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0023895 Liver diseases UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0007097 Carcinoma UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0017921 Glycogen storage disease type II UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0021400 Influenza UGT1A3 54659 UDP glucuronosyltransferase family 1 member A3 P35503
C0020433 Hyperbilirubinemia UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0024623 Malignant neoplasm of stomach UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0271979 Thalassemia Intermedia UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0017921 Glycogen storage disease type II UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0036572 Seizures UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0023473 Myeloid Leukemia, Chronic UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0017551 Gilbert Disease (disorder) UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0010324 Crigler Najjar syndrome, type 1 UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0039730 Thalassemia UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310
C0027947 Neutropenia UGT1A4 54657 UDP glucuronosyltransferase family 1 member A4 P22310

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Last updated: August 19, 2024