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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 |
| Disease ID | Disease Name | Gene Symbol | Gene ID ▼ | Gene Name | UniProt ID |
|---|---|---|---|---|---|
| C1140680 | Malignant neoplasm of ovary | FCN3 | 8547 | ficolin 3 | O75636 |
| C0003257 | Antibody Deficiency Syndrome | FCN3 | 8547 | ficolin 3 | O75636 |
| C0006826 | Malignant Neoplasms | FCN3 | 8547 | ficolin 3 | O75636 |
| C0023343 | Leprosy | FCN3 | 8547 | ficolin 3 | O75636 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | FCN3 | 8547 | ficolin 3 | O75636 |
| C0027051 | Myocardial Infarction | FCN3 | 8547 | ficolin 3 | O75636 |
| C0162871 | Aortic Aneurysm, Abdominal | FCN3 | 8547 | ficolin 3 | O75636 |
| C0024141 | Lupus Erythematosus, Systemic | FCN3 | 8547 | ficolin 3 | O75636 |
| C2239176 | Liver carcinoma | FCN3 | 8547 | ficolin 3 | O75636 |
| C3665596 | Warts | FCN3 | 8547 | ficolin 3 | O75636 |
| C0010346 | Crohn Disease | FCN3 | 8547 | ficolin 3 | O75636 |
| C0206062 | Lung Diseases, Interstitial | FCN3 | 8547 | ficolin 3 | O75636 |
| C0010068 | Coronary heart disease | FCN3 | 8547 | ficolin 3 | O75636 |
| C0020538 | Hypertensive disease | FCN3 | 8547 | ficolin 3 | O75636 |
| C0041296 | Tuberculosis | FCN3 | 8547 | ficolin 3 | O75636 |
| C0043037 | Common wart | FCN3 | 8547 | ficolin 3 | O75636 |
| C0919267 | ovarian neoplasm | FCN3 | 8547 | ficolin 3 | O75636 |
| C0036421 | Systemic Scleroderma | FCN3 | 8547 | ficolin 3 | O75636 |
| C4721610 | Carcinoma, Ovarian Epithelial | FCN3 | 8547 | ficolin 3 | O75636 |
| C0002736 | Amyotrophic Lateral Sclerosis | FCN3 | 8547 | ficolin 3 | O75636 |
| C0085580 | Essential Hypertension | FCN3 | 8547 | ficolin 3 | O75636 |
| C0004623 | Bacterial Infections | FCN3 | 8547 | ficolin 3 | O75636 |
| C0015934 | Fetal Growth Retardation | FCN3 | 8547 | ficolin 3 | O75636 |
| C0272242 | Complement deficiency disease | FCN3 | 8547 | ficolin 3 | O75636 |
| C0008925 | Cleft Palate | SELENOI | 85465 | selenoprotein I | Q9C0D9 |
