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prekallikrein deficiency

Disease Summary
Associated Targets (1)
Tclin

1


Mondo Description 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.
Uniprot Description This disorder is a blood coagulation defect.
Mondo Term and Equivalent IDs
MONDO:0044744:  prekallikrein deficiency
NCIT:C99022: 
SCTID:48976006: