eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | thrombophilia |
| Symptom | C0584960|factor v leiden mutation |
| Sentences | 1 |
| PubMedID- 25674132 | High prevalence of protein c, protein s, antithrombin deficiency, and factor v leiden mutation as a cause of hereditary thrombophilia in patients of venous thromboembolism and cerebrovascular accident. |
Page: 1