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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
acquired von Willebrand syndrome 
Bleeding Disorder, East Texas Type 
Bleeding Disorder, Vascular-Type  
Car Factor Deficiency 
Coagulation Protein Disorders +   
Deficiency of Plasma Clot Retraction Factor 
disseminated intravascular coagulation +   
Ecchymosis 
Fibrinolytic Defect 
Globulin Anomaly involving Beta (2A)-Globulin 
hemorrhagic disease +   
Hyperheparinemia 
Inherited Blood Coagulation Disease +   
Prekallikrein Deficiency  
This disease is a rare asymptomatic clotting defect characterized by prolongation of activated partial thromboplastin time
purpura +   
thrombophilia +   

Synonyms
Exact Synonyms: Fletcher Factor Deficiency ;   INHERITED PREKALLIKREIN DEFICIENCY ;   KLKB1-RELATED CONDITION ;   PKK Deficiency ;   PKKD
Primary IDs: MESH:C562725
Alternate IDs: OMIA:000819 ;   OMIM:612423
Definition Sources: OMIM:612423

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