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von Willebrand's disease (DOID:12531)
Annotations: Rat: (7) Mouse: (7) Human: (7) Chinchilla: (7) Bonobo: (7) Dog: (7) Squirrel: (7) Pig: (7)
Parent Terms Term With Siblings Child Terms
Activated Protein C Resistance  
alpha-2-plasmin inhibitor deficiency  
antithrombin III deficiency  
Bernard-Soulier syndrome +   
blood platelet disease +   
Chondrodysplasia Punctata with Coagulation Factor Deficiency 
congenital afibrinogenemia +   
Congenital Plasminogen Deficiency 
disseminated intravascular coagulation +   
Dysfibrinogenemia Causing Recurrent Thrombosis 
Ehlers-Danlos Syndrome with Platelet Dysfunction from Fibronectin Abnormality 
Essential Athrombia 
essential thrombocythemia  
factor V deficiency +   
factor VII deficiency  
factor VIII deficiency +   
factor X deficiency  
factor XI deficiency  
factor XII deficiency  
factor XIII deficiency +   
Factors VIII, IX and XI, Combined Deficiency of 
Familial Hemorrhagic Diathesis due to Antithrombin 
Familial Multiple Coagulation Factor Deficiency II 
Familial Multiple Coagulation Factor Deficiency IV 
Familial Multiple Coagulation Factor Deficiency VI 
Familial Platelet Disorder with Associated Myeloid Malignancy  
Flood Factor Deficiency 
Glanzmann's thrombasthenia +   
gray platelet syndrome +   
hemophilia B  
Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Cataracts  
Hermansky-Pudlak syndrome +   
high molecular weight kininogen deficiency  
MYH-9 related disease +   
Passovoy Factor 
Pechet Factor Deficiency 
Phospholipase A2, Group IVA, Deficiency of  
Plasminogen Activator Inhibitor-1 Deficiency  
Platelet Abnormalities with Eosinophilia and Immune-Mediated Inflammatory Disease  
Platelet Aggregation, Spontaneous 
Platelet Factor 3 Deficiency 
Platelet Prostacyclin Receptor Defect 
Platelet Receptor for Collagen, Deficiency of 
Platelet Signal Processing Defect 
platelet storage pool deficiency +   
platelet-type bleeding disorder 10  
platelet-type bleeding disorder 11  
platelet-type bleeding disorder 12 
Platelet-Type Bleeding Disorder 13  
platelet-type bleeding disorder 14  
platelet-type bleeding disorder 15  
platelet-type bleeding disorder 16  
platelet-type bleeding disorder 17  
platelet-type bleeding disorder 18  
platelet-type bleeding disorder 19  
platelet-type bleeding disorder 20  
Platelet-Type Bleeding Disorder 21  
Platelet-Type Bleeding Disorder 22  
platelet-type bleeding disorder 3  
platelet-type bleeding disorder 8  
platelet-type bleeding disorder 9  
Primary Release Disorder Of Platelets 
Prolonged Bleeding Time, Brachydactyly, and Mental Retardation  
protein C deficiency +   
prothrombin deficiency +   
Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency  
purpura +   
qualitative platelet defect 
Quebec platelet disorder  
Scott syndrome  
Stormorken syndrome  
Tatsumi Factor Deficiency 
thrombocytopenia +   
thrombocytosis +   
Undefined Platelet Disorder 
vascular hemostatic disease +   
vitamin K deficiency bleeding  
Vitamin K-Dependent Clotting Factors, Combined Deficiency Of, 1  
Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 2  
von Willebrand's disease +   
Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion.
Waterhouse-Friderichsen syndrome +  
White Platelet Syndrome 
Wiskott-Aldrich syndrome +   
X-Linked Anemia with or without Neutropenia and/or Platelet Abnormalities  

Exact Synonyms: Angiohemophilia ;   Angiohemophilias ;   Vascular Hemophilia ;   Vascular Hemophilias ;   Vascular Pseudohemophilia ;   Vascular Pseudohemophilias ;   Von Willebrand Disorder ;   Von Willebrand's Factor Deficiency ;   von Willebrand Disease ;   von Willebrand Disease, Recessive Form ;   von Willebrand diseases ;   von Willebrand's Diseases ;   von Willebrand's-Jurgens' disease ;   von Willebrand-Jrgens disease
Primary IDs: MESH:D014842 ;   RDO:0000238
Xrefs: GARD:7867 ;   ICD10CM:D68.0 ;   ICD10CM:D69.8 ;   ICD9CM:286.4 ;   NCI:C68677
Definition Sources: MESH:D014842,,

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