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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
acquired coagulation factor deficiency +  
acquired hemophilia +  
acquired von willebrand syndrome 
alpha-2-plasmin inhibitor deficiency 
autoimmune thrombocytopenic purpura 
combined deficiency of factor V and factor VIII +  
congenital factor V deficiency 
congenital factor XI deficiency 
congenital factor XII deficiency 
congenital factor XIII deficiency +  
congenital fibrinogen deficiency +  
congenital high-molecular-weight kininogen deficiency 
congenital plasminogen activator inhibitor type 1 deficiency 
congenital thrombotic thrombocytopenic purpura 
congenital vitamin K-dependent coagulation factors deficiency +  
cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder 
East Texas bleeding disorder 
Ehlers-Danlos syndrome, fibronectinemic type 
factor V and factor VIII, combined deficiency of, type 1 
factor V deficiency +  
factor VII deficiency +  
factor X deficiency +  
factor XIII deficiency +  
factor XIII, A subunit, deficiency of 
familial thrombomodulin anomalies 
fetal and neonatal alloimmune thrombocytopenia 
Glanzmann thrombasthenia +  
hemophilia +  
hemophilia A +  
hemophilia B +  
hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation 
hereditary hemolytic uremic syndrome +  
hereditary thrombocytopenia and hematologic cancer predisposition syndrome +  
hereditary thrombocytosis with transverse limb defect 
hereditary von Willebrand disease +  
Hermansky-Pudlak syndrome +  
hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency 
hypoplasminogenemia 
inherited bleeding disorder, platelet-type +  
inherited prekallikrein deficiency 
An instance of prekallikrein deficiency that is caused by an inherited modification of the individual's genome.
inherited thrombophilia +  
multiple sclerosis-ichthyosis-factor VIII deficiency syndrome 
platelet-type bleeding disorder 10 
platelet-type bleeding disorder 14 
platelet-type bleeding disorder 18 
platelet-type bleeding disorder 8 
prothrombin deficiency +  
purpura +  
Scott syndrome 
thrombomodulin-related bleeding disorder 
thrombophilia due to activated protein C resistance 
vascular hemostatic disease +  
von Willebrand disease (hereditary or acquired) +  
Wiskott-Aldrich syndrome 

Synonyms
Exact Synonyms: fletcher factor (prekallikrein) deficiency ;   hereditary prekallikrein deficiency
Related Synonyms: Fletcher Factor deficiency ;   PKK deficiency ;   prekallikrein deficiency ;   prekallikrein deficiency, congenital
Alternate IDs: MONDO:0012901
Xrefs: GARD:4477 ;   ICD9:286.9 ;   MESH:C562725 ;   NANDO:2200684 ;   OMIM:612423 ;   ORDO:749
see_also: https://rarediseases.info.nih.gov/diseases/4477/prekallikrein-deficiency-congenital xsd:anyURI {source="GARD:0004477"}
Definition Sources: MONDO:patterns/hereditary

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