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 61776 - 61800 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0004352 Autistic Disorder OGG1 4968 8-oxoguanine DNA glycosylase O15527
C0151744 Myocardial Ischemia OGG1 4968 8-oxoguanine DNA glycosylase O15527
C0740392 Infarction, Middle Cerebral Artery OGG1 4968 8-oxoguanine DNA glycosylase O15527
C0011884 Diabetic Retinopathy OGG1 4968 8-oxoguanine DNA glycosylase O15527
C0018213 Graves Disease OGG1 4968 8-oxoguanine DNA glycosylase O15527
C0085669 Acute leukemia OGG1 4968 8-oxoguanine DNA glycosylase O15527
C0007107 Malignant neoplasm of larynx OGG1 4968 8-oxoguanine DNA glycosylase O15527
C0030319 Panic Disorder OGG1 4968 8-oxoguanine DNA glycosylase O15527
C0010054 Coronary Arteriosclerosis OGG1 4968 8-oxoguanine DNA glycosylase O15527
C0010068 Coronary heart disease OGG1 4968 8-oxoguanine DNA glycosylase O15527
C0004763 Barrett Esophagus OGG1 4968 8-oxoguanine DNA glycosylase O15527
C0007113 Rectal Carcinoma OGG1 4968 8-oxoguanine DNA glycosylase O15527
C0345905 Intrahepatic Cholangiocarcinoma OGG1 4968 8-oxoguanine DNA glycosylase O15527
C0022593 Keratosis OGG1 4968 8-oxoguanine DNA glycosylase O15527
C0279651 Gallbladder adenocarcinoma OGG1 4968 8-oxoguanine DNA glycosylase O15527
C0035934 Rubinstein-Taybi Syndrome OGG1 4968 8-oxoguanine DNA glycosylase O15527
C0343641 Human papilloma virus infection OGG1 4968 8-oxoguanine DNA glycosylase O15527
C0393574 Huntington Disease, Late Onset OGG1 4968 8-oxoguanine DNA glycosylase O15527
C0023895 Liver diseases OGG1 4968 8-oxoguanine DNA glycosylase O15527
C0026613 Motor Skills Disorders OGG1 4968 8-oxoguanine DNA glycosylase O15527
C3160718 PARKINSON DISEASE, LATE-ONSET OGG1 4968 8-oxoguanine DNA glycosylase O15527
C0268579 Propionic acidemia OGG1 4968 8-oxoguanine DNA glycosylase O15527
C2713347 7-Dehydrocholesterol Reductase Deficiency DHCR7 1717 7-dehydrocholesterol reductase Q9UBM7
C0175694 Smith-Lemli-Opitz Syndrome DHCR7 1717 7-dehydrocholesterol reductase Q9UBM7
C0036439 Scoliosis, unspecified DHCR7 1717 7-dehydrocholesterol reductase Q9UBM7

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Last updated: August 19, 2024