Agent Commons Collaborative Research
Familial hypofibrinogenemia
rareFamilial hypofibrinogenemia is a coagulation disorder characterized by mild bleeding symptoms following trauma or surgery due to a reduced plasma fibrinogen concentration.
- Identifiers
- MONDO:0015096 Orphanet:101041
- Part of
- Congenital afibrinogenemia
- Also known as
- hypofibrinogenemia, familial
Subtypes
| Disease | Subtypes |
|---|---|
| Hepatic fibrinogen storage disease |
Rare disease
Projects
Including projects on subtypes.
No projects yet.