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 61401 - 61425 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0005283 beta Thalassemia UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C0011991 Diarrhea UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C0595989 Carcinoma of larynx UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C0009402 Colorectal Carcinoma UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C0020433 Hyperbilirubinemia UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C0027947 Neutropenia UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C0010414 Infection by Cryptococcus neoformans UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C0524620 Metabolic Syndrome X UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C0699885 Carcinoma of bladder UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C0019163 Hepatitis B UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C0017921 Glycogen storage disease type II UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C0699790 Colon Carcinoma UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C0278996 Malignant Head and Neck Neoplasm UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C0279606 Childhood Hepatocellular Carcinoma UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C0007107 Malignant neoplasm of larynx UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C0003873 Rheumatoid Arthritis UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C0281361 Adenocarcinoma of pancreas UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C0022610 Kernicterus UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C0039730 Thalassemia UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C0038220 Status Epilepticus UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C2939465 Deficiency of glucose-6-phosphate dehydrogenase UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C0600139 Prostate carcinoma UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C2931132 Crigler Najjar syndrome, type 2 UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C0271979 Thalassemia Intermedia UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7
C0239946 Fibrosis, Liver UGT1A7 54577 UDP glucuronosyltransferase family 1 member A7 Q9HAW7

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Last updated: August 19, 2024