Agent Commons Collaborative Research
Prekallikrein deficiency
rareA condition characterized by the congenital or acquired deficiency of prekallikrein. This deficiency is usually not associated with bleeding. The congenital deficiency is very rare. Acquired deficiency may occur in diffuse intravascular coagulation, infections, and sickle cell disease.
- Identifiers
- MONDO:0044744
- Part of
- Blood coagulation disease
Subtypes
| Disease | Subtypes |
|---|---|
| Inherited prekallikrein deficiency |
Projects
Including projects on subtypes.
No projects yet.