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 |
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