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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
acquired factor XIII deficiency 
acquired hemophilia +  
acquired von willebrand syndrome 
alpha-2-plasmin inhibitor deficiency 
combined deficiency of factor V and factor VIII +  
congenital agammaglobulinemia +  
congenital amegakaryocytic thrombocytopenia 1 
congenital analbuminemia 
congenital anemia +  
congenital factor V deficiency 
congenital factor XI deficiency 
congenital factor XII deficiency 
congenital factor XIII deficiency +  
Congenital factor XIII deficiency is an inherited bleeding disorder due to reduced levels and activity of factor XIII (FXIII) and characterized by hemorrhagic diathesis frequently associated with spontaneous abortions and defective wound healing. Factor XIII deficiency is one of the most rare coagulation factor deficiencies.
congenital fibrinogen deficiency +  
congenital high-molecular-weight kininogen deficiency 
congenital plasminogen activator inhibitor type 1 deficiency 
congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome 
congenital secondary polycythemia +  
congenital thrombotic thrombocytopenic purpura 
congenital vitamin K-dependent coagulation factors deficiency +  
constitutional neutropenia +  
East Texas bleeding disorder 
factor VII deficiency +  
factor X deficiency +  
fetal and neonatal alloimmune thrombocytopenia 
GNE myopathy 
hemophilia A +  
hemophilia B +  
hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation 
hereditary thrombocytosis with transverse limb defect 
hereditary von Willebrand disease +  
hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency 
inherited bleeding disorder, platelet-type +  
inherited prekallikrein deficiency 
leukocyte adhesion deficiency type II 
macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome 
multiple sclerosis-ichthyosis-factor VIII deficiency syndrome 
prothrombin deficiency +  
purpura +  
radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome 
thrombocytopenia-absent radius syndrome 
thrombomodulin-related bleeding disorder 
vascular hemostatic disease +  

Synonyms
Exact Synonyms: deficiency, Laki-Lorand factor ;   factor XIII deficiency disease ;   hereditary factor XIII deficiency disease
Related Synonyms: factor XIII deficiency ;   fibrin stabilising factor deficiency ;   fibrin stabilizing factor deficiency
Alternate IDs: MONDO:0018029
Xrefs: DOID:2211 ;   GARD:10766 ;   ICD9:286.3 ;   NANDO:2200681 ;   NCI:C131633 ;   ORDO:331 ;   SCTID:50189006
Definition Sources: Orphanet:331

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