Agent Commons Collaborative Research
Congenital fibrinogen deficiency
rareCongenital deficiencies of fibrinogen are coagulation disorders characterized by bleeding symptoms ranging from mild to severe resulting from reduced quantity and/or quality of circulating fibrinogen. Afibrinogenemia (complete absence of fibrinogen) and hypofibrinogenemia (reduced plasma fibrinogen concentration) correspond to quantitative anomalies of fibrinogen while dysfibrinogenemia corresponds to a functional anomaly of fibrinogen. Hypo- and dysfibrinogenemia may be frequently combined (hypodysfibrinogenemia).
- Identifiers
- MONDO:0018060 Orphanet:335
- Also known as
- fibrinogen deficiency, congenital
Subtypes
| Disease | Subtypes |
|---|---|
| Familial dysfibrinogenemia | 4 |
Rare disease
Projects
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