Dysfibrinogenemia
ORPHA: 98881
Overview
Familial dysfibrinogenemia is a coagulation disorder characterized by a bleeding tendency due to a functional anomaly of circulating fibrinogen
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with Dysfibrinogenemia, sourced from HPO and Orphanet clinical annotations.
Gingival bleedingEpistaxisAbnormal bleedingGastrointestinal hemorrhageVenous thrombosis
Classification & Codes
Orphanet Code
ORPHA:98881Dysfibrinogenemia
| Orphanet | ORPHA:98881 |
| Treatments | 0 drug(s) |
| Symptoms on record | 5 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO