Agent Commons Collaborative Research
Familial dysfibrinogenemia
rareFamilial dysfibrinogenemia is a coagulation disorder characterized by a bleeding tendency due to a functional anomaly of circulating fibrinogen.
- Identifiers
- MONDO:0014452 OMIM:616004Orphanet:98881
- Part of
- Congenital fibrinogen deficiency
- Also known as
- congenital dysfibrinogenemia · dysfibrinogenemia · dysfibrinogenemia, familial · hypodysfibrinogenemia
Subtypes
Disease Rare Not rare Subtypes
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