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 1951 - 1975 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0684249 Carcinoma of lung SCD 6319 stearoyl-CoA desaturase O00767
C0345904 Malignant neoplasm of liver SCD 6319 stearoyl-CoA desaturase O00767
C0002395 Alzheimer's Disease SCD 6319 stearoyl-CoA desaturase O00767
C0022658 Kidney Diseases SCD 6319 stearoyl-CoA desaturase O00767
C0023976 Long QT Syndrome SCD 6319 stearoyl-CoA desaturase O00767
C0919267 ovarian neoplasm SCD 6319 stearoyl-CoA desaturase O00767
C0878544 Cardiomyopathies SCD 6319 stearoyl-CoA desaturase O00767
C0023794 Lipoidosis SCD 6319 stearoyl-CoA desaturase O00767
C0018801 Heart failure SCD 6319 stearoyl-CoA desaturase O00767
C0007097 Carcinoma SCD 6319 stearoyl-CoA desaturase O00767
C0030567 Parkinson Disease SCD 6319 stearoyl-CoA desaturase O00767
C0024796 Marfan Syndrome SCD 6319 stearoyl-CoA desaturase O00767
C0025202 melanoma SCD 6319 stearoyl-CoA desaturase O00767
C0019829 Hodgkin Disease SCD 6319 stearoyl-CoA desaturase O00767
C0005283 beta Thalassemia SCD 6319 stearoyl-CoA desaturase O00767
C0003850 Arteriosclerosis SCD 6319 stearoyl-CoA desaturase O00767
C0011847 Diabetes SCD 6319 stearoyl-CoA desaturase O00767
C0524620 Metabolic Syndrome X SCD 6319 stearoyl-CoA desaturase O00767
C0017638 Glioma SCD 6319 stearoyl-CoA desaturase O00767
C0011860 Diabetes Mellitus, Non-Insulin-Dependent SCD 6319 stearoyl-CoA desaturase O00767
C0020474 Hyperlipidemia, Familial Combined SCD 6319 stearoyl-CoA desaturase O00767
C0018802 Congestive heart failure SCD 6319 stearoyl-CoA desaturase O00767
C0019045 Hemoglobinopathies SCD 6319 stearoyl-CoA desaturase O00767
C0007102 Malignant tumor of colon SCD 6319 stearoyl-CoA desaturase O00767
C0003125 Anorexia Nervosa SCD 6319 stearoyl-CoA desaturase O00767

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