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 1226 - 1250 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0022658 Kidney Diseases TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0037116 Silicosis TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0264694 Chronic myocardial ischemia TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0235833 Congenital diaphragmatic hernia TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0020541 Portal Hypertension TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0034069 Pulmonary Fibrosis TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0699885 Carcinoma of bladder TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0011849 Diabetes Mellitus TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0085584 Encephalopathies TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0020538 Hypertensive disease TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0243026 Sepsis TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0003850 Arteriosclerosis TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0029456 Osteoporosis TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0740391 Middle Cerebral Artery Occlusion TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0030305 Pancreatitis TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0406500 Lipodermatosclerosis TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0027051 Myocardial Infarction TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0011860 Diabetes Mellitus, Non-Insulin-Dependent TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0032285 Pneumonia TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0011847 Diabetes TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0035344 Retinopathy of Prematurity TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0007222 Cardiovascular Diseases TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0027697 Nephritis TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C1306459 Primary malignant neoplasm TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0007785 Cerebral Infarction TM7SF2 7108 transmembrane 7 superfamily member 2 O76062

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Last updated: August 19, 2024