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 51801 - 51825 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0011633 Dermatomyositis SOAT1 6646 sterol O-acyltransferase 1 P35610
C0085413 Polycystic Kidney, Autosomal Dominant SOAT1 6646 sterol O-acyltransferase 1 P35610
C0152013 Adenocarcinoma of lung (disorder) SOAT1 6646 sterol O-acyltransferase 1 P35610
C0029456 Osteoporosis SOAT1 6646 sterol O-acyltransferase 1 P35610
C0920350 Autoimmune thyroiditis SOAT1 6646 sterol O-acyltransferase 1 P35610
C0005684 Malignant neoplasm of urinary bladder SOAT1 6646 sterol O-acyltransferase 1 P35610
C0009691 Congenital cataract SORD 6652 sorbitol dehydrogenase Q00796
C0600139 Prostate carcinoma SORD 6652 sorbitol dehydrogenase Q00796
C0027651 Neoplasms SORD 6652 sorbitol dehydrogenase Q00796
C0027819 Neuroblastoma SORD 6652 sorbitol dehydrogenase Q00796
C0030421 Paraganglioma SORD 6652 sorbitol dehydrogenase Q00796
C0400966 Non-alcoholic Fatty Liver Disease SORD 6652 sorbitol dehydrogenase Q00796
C0006826 Malignant Neoplasms SORD 6652 sorbitol dehydrogenase Q00796
C0007134 Renal Cell Carcinoma SORD 6652 sorbitol dehydrogenase Q00796
C0030422 Extra-Adrenal Paraganglioma SORD 6652 sorbitol dehydrogenase Q00796
C0031511 Pheochromocytoma SORD 6652 sorbitol dehydrogenase Q00796
C0022658 Kidney Diseases SORD 6652 sorbitol dehydrogenase Q00796
C0549473 Thyroid carcinoma SORD 6652 sorbitol dehydrogenase Q00796
C1334699 Mesenchymal Cell Neoplasm SORD 6652 sorbitol dehydrogenase Q00796
C0005695 Bladder Neoplasm SORD 6652 sorbitol dehydrogenase Q00796
C1306459 Primary malignant neoplasm SORD 6652 sorbitol dehydrogenase Q00796
C0279702 Conventional (Clear Cell) Renal Cell Carcinoma SORD 6652 sorbitol dehydrogenase Q00796
C0238198 Gastrointestinal Stromal Tumors SORD 6652 sorbitol dehydrogenase Q00796
C0265338 Coffin-Siris syndrome SORD 6652 sorbitol dehydrogenase Q00796
C1855008 Mitochondrial Complex II Deficiency SORD 6652 sorbitol dehydrogenase Q00796

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Last updated: August 19, 2024