Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
alpha-2-plasmin inhibitor deficiency  
Bernard-Soulier syndrome +   
blood platelet disease +   
Disorders caused by abnormalities in platelet count or function.
congenital afibrinogenemia +   
disseminated intravascular coagulation +   
essential thrombocythemia  
factor V deficiency +   
factor VII deficiency  
factor VIII deficiency +   
factor X deficiency  
factor XI deficiency  
factor XII deficiency  
factor XIII deficiency +   
Familial Hemorrhagic Diathesis due to Antithrombin 
Glanzmann's thrombasthenia +   
hemophilia B  
Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Cataracts  
Plasminogen Activator Inhibitor-1 Deficiency  
platelet storage pool deficiency +   
prothrombin deficiency +   
purpura +   
vascular hemostatic disease +   
vitamin K deficiency bleeding  
von Willebrand's disease +   
Waterhouse-Friderichsen syndrome +  
Wiskott-Aldrich syndrome +   

Synonyms
Exact Synonyms: Thrombocytopathies ;   blood platelet disorder ;   blood platelet disorders ;   platelet disorder ;   thrombocytopathy
Narrow Synonyms: Thrombopathia
Primary IDs: MESH:D001791
Alternate IDs: OMIA:001003 ;   RDO:0002359
Xrefs: OMIM:PS231200
Definition Sources: MESH:D001791

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.