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Ontology Browser
Term:
combined deficiency of factor V and factor VIII (EFO:MONDO:0018175)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0) Naked Mole-rat: (0) Green Monkey: (0)
Parent Terms Term With Siblings Child Terms
acquired coagulation factor deficiency +  
acquired hemophilia +  
acquired von willebrand syndrome 
alpha-2-plasmin inhibitor deficiency 
combined deficiency of factor V and factor VIII +  
Combined deficiency of factor V and factor VIII is an inherited bleeding disorder due to the reduction in activity and antigen levels of both factor V (FV) and factor VIII (FVIII) and characterized by mild-to-moderate bleeding symptoms.
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 vitamin K-dependent coagulation factors deficiency +  
East Texas bleeding disorder 
factor V deficiency +  
factor VII deficiency +  
factor X deficiency +  
factor XIII deficiency +  
fetal and neonatal alloimmune thrombocytopenia 
hemophilia +  
hemophilia A +  
hemophilia B +  
hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation 
hereditary von Willebrand disease +  
hypoplasminogenemia 
inherited bleeding disorder, platelet-type +  
inherited prekallikrein deficiency 
multiple sclerosis-ichthyosis-factor VIII deficiency syndrome 
prothrombin deficiency +  
purpura +  
thrombomodulin-related bleeding disorder 
thrombophilia due to activated protein C resistance 
vascular hemostatic disease +  
von Willebrand disease (hereditary or acquired) +  

Synonyms
Exact Synonyms: F5F8D ;   FV and FVIII combined deficiency ;   combined deficiency of factor V and factor type VIII ;   familial multiple coagulation factor deficiency
Alternate IDs: MONDO:0018175
Xrefs: GARD:16639 ;   MEDGEN:384006 ;   NANDO:2200686 ;   ORDO:35909 ;   SCTID:715559004 ;   UMLS:C1856883
Definition Sources: Orphanet:35909

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