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 4751 - 4775 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0699791 Stomach Carcinoma UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0023895 Liver diseases UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0036341 Schizophrenia UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0342751 Generalized glycogen storage disease of infants UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C1704272 Benign Prostatic Hyperplasia UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0022610 Kernicterus UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0024623 Malignant neoplasm of stomach UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0037889 Hereditary spherocytosis UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0268138 Xeroderma Pigmentosum, Complementation Group D UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0042133 Uterine Fibroids UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0036572 Seizures UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0023473 Myeloid Leukemia, Chronic UGT1A10 54575 UDP glucuronosyltransferase family 1 member A10 Q9HAW8
C0020433 Hyperbilirubinemia UGT1A10 54575 UDP glucuronosyltransferase family 1 member A10 Q9HAW8
C0342751 Generalized glycogen storage disease of infants UGT1A10 54575 UDP glucuronosyltransferase family 1 member A10 Q9HAW8
C0600139 Prostate carcinoma UGT1A10 54575 UDP glucuronosyltransferase family 1 member A10 Q9HAW8
C0376358 Malignant neoplasm of prostate UGT1A10 54575 UDP glucuronosyltransferase family 1 member A10 Q9HAW8
C2239176 Liver carcinoma UGT1A10 54575 UDP glucuronosyltransferase family 1 member A10 Q9HAW8
C0017551 Gilbert Disease (disorder) UGT1A10 54575 UDP glucuronosyltransferase family 1 member A10 Q9HAW8
C0027947 Neutropenia UGT1A10 54575 UDP glucuronosyltransferase family 1 member A10 Q9HAW8
C0002895 Anemia, Sickle Cell UGT1A10 54575 UDP glucuronosyltransferase family 1 member A10 Q9HAW8
C1306459 Primary malignant neoplasm UGT1A10 54575 UDP glucuronosyltransferase family 1 member A10 Q9HAW8
C0149925 Small cell carcinoma of lung UGT1A10 54575 UDP glucuronosyltransferase family 1 member A10 Q9HAW8
C0008350 Cholelithiasis UGT1A10 54575 UDP glucuronosyltransferase family 1 member A10 Q9HAW8
C0038356 Stomach Neoplasms UGT1A10 54575 UDP glucuronosyltransferase family 1 member A10 Q9HAW8
C0017205 Gaucher Disease UGT1A10 54575 UDP glucuronosyltransferase family 1 member A10 Q9HAW8

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Last updated: August 19, 2024