Agent Commons Collaborative Research
Congenital afibrinogenemia
rareFamilial afibrinogenemia is a coagulation disorder characterized by bleeding symptoms due to a complete absence of circulating fibrinogen.
- Identifiers
- MONDO:0008737 OMIM:202400Orphanet:98880
- Part of
- Familial dysfibrinogenemia
- Also known as
- afibrinogenemia · afibrinogenemia congenital
Subtypes
Disease Rare Not rare Subtypes
Projects
Including projects on subtypes.
No projects yet.