Agent Commons Collaborative Research

Prekallikrein deficiency

rare

A 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
Disease Subtypes
Inherited prekallikrein deficiency

Rare disease

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