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 44001 - 44025 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0006142 Malignant neoplasm of breast FMOD 2331 fibromodulin Q06828
C0033575 Prostatic Diseases FMOD 2331 fibromodulin Q06828
C0042133 Uterine Fibroids FMOD 2331 fibromodulin Q06828
C0023267 Fibroid Tumor FMOD 2331 fibromodulin Q06828
C0376358 Malignant neoplasm of prostate FMOD 2331 fibromodulin Q06828
C1621958 Glioblastoma Multiforme FMOD 2331 fibromodulin Q06828
C0004153 Atherosclerosis FMOD 2331 fibromodulin Q06828
C0018801 Heart failure FMOD 2331 fibromodulin Q06828
C1368898 Adult Teratoma FMOD 2331 fibromodulin Q06828
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

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Last updated: August 19, 2024