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 48476 - 48500 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0001175 Acquired Immunodeficiency Syndrome CD14 929 CD14 molecule P08571
C0442874 Neuropathy CD14 929 CD14 molecule P08571
C0595989 Carcinoma of larynx CD14 929 CD14 molecule P08571
C0022650 Kidney Calculi CD14 929 CD14 molecule P08571
C0162296 Polyarthralgia CD14 929 CD14 molecule P08571
C0346647 Malignant neoplasm of pancreas CD14 929 CD14 molecule P08571
C4721610 Carcinoma, Ovarian Epithelial CD14 929 CD14 molecule P08571
C0524620 Metabolic Syndrome X CD14 929 CD14 molecule P08571
C0017661 IGA Glomerulonephritis CD14 929 CD14 molecule P08571
C0007785 Cerebral Infarction CD14 929 CD14 molecule P08571
C0016470 Food Allergy CD14 929 CD14 molecule P08571
C0019829 Hodgkin Disease CD14 929 CD14 molecule P08571
C0027831 Neurofibromatosis 1 CD14 929 CD14 molecule P08571
C0013537 Eclampsia CD14 929 CD14 molecule P08571
C0018099 Gout CD14 929 CD14 molecule P08571
C1332986 Childhood Osteosarcoma CD14 929 CD14 molecule P08571
C0019621 Histiocytosis, Langerhans-Cell CD14 929 CD14 molecule P08571
C0242379 Malignant neoplasm of lung CD14 929 CD14 molecule P08571
C4520983 Congenital atresia of extrahepatic bile duct CD14 929 CD14 molecule P08571
C0029227 Delirium, Dementia, Amnestic, Cognitive Disorders CD14 929 CD14 molecule P08571
C0268186 Congenital glucose-galactose malabsorption CD14 929 CD14 molecule P08571
C0008312 Primary biliary cirrhosis CD14 929 CD14 molecule P08571
C1861172 Venous Thromboembolism CD14 929 CD14 molecule P08571
C0024894 Mastitis CD14 929 CD14 molecule P08571
C0019158 Hepatitis CD14 929 CD14 molecule P08571

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Last updated: August 19, 2024