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 53376 - 53400 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0024439 Macular corneal dystrophy LCAT 3931 lecithin-cholesterol acyltransferase P04180
C0033687 Proteinuria LCAT 3931 lecithin-cholesterol acyltransferase P04180
C0013238 Dry Eye Syndromes LCAT 3931 lecithin-cholesterol acyltransferase P04180
C3665347 Visual Impairment LCAT 3931 lecithin-cholesterol acyltransferase P04180
C0039292 Tangier Disease LCAT 3931 lecithin-cholesterol acyltransferase P04180
C2239176 Liver carcinoma LCAT 3931 lecithin-cholesterol acyltransferase P04180
C0155733 Atherosclerosis of aorta LCAT 3931 lecithin-cholesterol acyltransferase P04180
C0022658 Kidney Diseases LCAT 3931 lecithin-cholesterol acyltransferase P04180
C4721610 Carcinoma, Ovarian Epithelial LCAT 3931 lecithin-cholesterol acyltransferase P04180
C0002895 Anemia, Sickle Cell LCAT 3931 lecithin-cholesterol acyltransferase P04180
C0027888 Hereditary Motor and Sensory Neuropathies LCAT 3931 lecithin-cholesterol acyltransferase P04180
C3665365 Arteriosclerotic cardiovascular disease, NOS LCAT 3931 lecithin-cholesterol acyltransferase P04180
C0005859 Bloom Syndrome LCAT 3931 lecithin-cholesterol acyltransferase P04180
C0018802 Congestive heart failure LCAT 3931 lecithin-cholesterol acyltransferase P04180
C0178664 Glomerulosclerosis (disorder) LCAT 3931 lecithin-cholesterol acyltransferase P04180
C1140680 Malignant neoplasm of ovary LCAT 3931 lecithin-cholesterol acyltransferase P04180
C1636149 Macular dystrophy, corneal type 1 LCAT 3931 lecithin-cholesterol acyltransferase P04180
C0577631 Carotid Atherosclerosis LCAT 3931 lecithin-cholesterol acyltransferase P04180
C0027051 Myocardial Infarction LCAT 3931 lecithin-cholesterol acyltransferase P04180
C0524851 Neurodegenerative Disorders PRNP 5621 prion protein P04156
C1852467 Creutzfeldt-Jakob Disease, Sporadic PRNP 5621 prion protein P04156
C0162534 Prion Diseases PRNP 5621 prion protein P04156
C0002395 Alzheimer's Disease PRNP 5621 prion protein P04156
C0006142 Malignant neoplasm of breast PRNP 5621 prion protein P04156
C0017495 Gerstmann-Straussler-Scheinker Disease PRNP 5621 prion protein P04156

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Last updated: August 19, 2024