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Ontology Browser

Parent Terms Term With Siblings Child Terms
acquired von Willebrand syndrome 
alpha-2-plasmin inhibitor deficiency  
Bernard-Soulier syndrome +   
Bleeding Disorder, East Texas Type 
blood platelet disease +   
Car Factor Deficiency 
coagulation protein disease +   
congenital afibrinogenemia +   
disseminated intravascular coagulation +   
essential thrombocythemia  
A clinical syndrome characterized by repeated spontaneous hemorrhages and a remarkable increase in the number of circulating platelets.
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 
Fibrinolytic Defect 
Glanzmann's thrombasthenia +   
Globulin Anomaly involving Beta (2A)-Globulin 
hemophilia B  
Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Cataracts  
hemorrhagic disease +   
inherited blood coagulation disease +   
myeloproliferative disorder with eosinophilia  
Plasma Clot Retraction Factor, Deficiency of 
Plasminogen Activator Inhibitor-1 Deficiency  
platelet storage pool deficiency +   
Platelet-Type Bleeding Disorder 13  
platelet-type bleeding disorder 14  
polycythemia vera +   
Prekallikrein Deficiency  
protein S deficiency +   
prothrombin deficiency +   
purpura +   
Thrombocythemia 2  
Thrombocythemia 3  
Thrombocythemia, X-Linked 
Thrombocytosis, Benign Familial Microcytic  
Thrombocytosis, Familial X-Linked 
thrombophilia +   
transient myeloproliferative syndrome  
vascular hemostatic disease +   
vitamin K deficiency bleeding  
von Willebrand's disease +   
Waterhouse-Friderichsen syndrome +  
Wiskott-Aldrich syndrome +   

Exact Synonyms: Autosomal Dominant Thrombocytoses ;   Autosomal Dominant Thrombocytosis ;   Essential Thrombocythemias ;   Hemorrhagic Thrombocythemia ;   Hemorrhagic Thrombocythemias ;   Idiopathic Thrombocythemia ;   Idiopathic Thrombocythemias ;   Primary Thrombocythemia ;   Primary Thrombocythemias ;   Primary Thrombocytoses ;   Primary Thrombocytosis ;   THCYT1 ;   essential thrombocythaemia ;   familial thrombocytosis ;   hereditary thrombocythemia ;   thrombocythemia 1 ;   thrombocytosis 1
Narrow Synonyms: familial essential thrombocythemia
Primary IDs: MESH:D013920
Alternate IDs: OMIM:187950 ;   RDO:0006690
Xrefs: GARD:6594 ;   ICD10CM:D47.3 ;   ICD9CM:238.71 ;   NCI:C3407 ;   ORDO:3318 ;   ORDO:71493
Definition Sources: MESH:D013920,

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