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 40376 - 40400 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0017636 Glioblastoma FMOD 2331 fibromodulin Q06828
C1332979 Childhood Lymphoma FMOD 2331 fibromodulin Q06828
C0039503 Tendinitis FMOD 2331 fibromodulin Q06828
C0024299 Lymphoma FMOD 2331 fibromodulin Q06828
C0334634 Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse FMOD 2331 fibromodulin Q06828
C0029408 Degenerative polyarthritis FMOD 2331 fibromodulin Q06828
C0242383 Age related macular degeneration FMOD 2331 fibromodulin Q06828
C0018802 Congestive heart failure FMOD 2331 fibromodulin Q06828
C0022658 Kidney Diseases FMOD 2331 fibromodulin Q06828
C0242852 Proliferative vitreoretinopathy FMOD 2331 fibromodulin Q06828
C0678222 Breast Carcinoma FMOD 2331 fibromodulin Q06828
C0079731 B-Cell Lymphomas FMOD 2331 fibromodulin Q06828
C0003850 Arteriosclerosis FMOD 2331 fibromodulin Q06828
C1864111 MYOPIA 3 (disorder) FMOD 2331 fibromodulin Q06828
C1332977 Childhood Leukemia FMOD 2331 fibromodulin Q06828
C0042025 Urinary Stress Incontinence FMOD 2331 fibromodulin Q06828
C0699790 Colon Carcinoma FMOD 2331 fibromodulin Q06828
C0149925 Small cell carcinoma of lung FMOD 2331 fibromodulin Q06828
C1332206 Adult Lymphoma FMOD 2331 fibromodulin Q06828
C0023418 leukemia FMOD 2331 fibromodulin Q06828
C0410174 Fukuyama Type Congenital Muscular Dystrophy FKTN 2218 fukutin O75072
C0003466 Anus, Imperforate FKTN 2218 fukutin O75072
C0521694 Atrophic retina FKTN 2218 fukutin O75072
C0265221 Walker-Warburg congenital muscular dystrophy FKTN 2218 fukutin O75072
C0006826 Malignant Neoplasms FKTN 2218 fukutin O75072

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Last updated: August 19, 2024