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von Willebrand Diseases
MeSH Headingvon Willebrand Diseases
Tree NumberC15.378.100.100.900
Tree NumberC15.378.100.141.900
Tree NumberC15.378.140.900
Tree NumberC15.378.463.920
Tree NumberC16.320.099.920
Annotationnote specific types of Von Willebrand Disease are available
Scope NoteGroup 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.
Entry TermAngiohemophilia
Entry TermHemophilia, Vascular
Entry Termvon Willebrand Disease
Entry Termvon Willebrand Disease, Recessive Form
Entry Termvon Willebrand's Disease
Entry Termvon Willebrand's Diseases
Allowable QualifiersBL CF CI CL CO DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RA RH RI RT SU TH UR US VE VI
History Note2010(1963)
Date of Entry19990101
Unique IDD014842


MeSH Tree Structures

 
Hemic and Lymphatic Diseases [C15]
   Hematologic Diseases [C15.378]
      Blood Coagulation Disorders [C15.378.100]
         Blood Coagulation Disorders, Inherited [C15.378.100.100]
Activated Protein C Resistance [C15.378.100.100.037]
Afibrinogenemia [C15.378.100.100.056]
Antithrombin III Deficiency [C15.378.100.100.075]
Bernard-Soulier Syndrome [C15.378.100.100.080]
Factor V Deficiency [C15.378.100.100.300]
Factor VII Deficiency [C15.378.100.100.310]
Factor X Deficiency [C15.378.100.100.320]
Factor XI Deficiency [C15.378.100.100.325]
Factor XII Deficiency [C15.378.100.100.330]
Factor XIII Deficiency [C15.378.100.100.335]
Hemophilia A [C15.378.100.100.500]
Hemophilia B [C15.378.100.100.510]
Hermanski-Pudlak Syndrome [C15.378.100.100.515]
Hypoprothrombinemias [C15.378.100.100.550]
Protein C Deficiency [C15.378.100.100.690]
Thrombasthenia [C15.378.100.100.820]
Arrow pointing to current tree nodevon Willebrand Diseases [C15.378.100.100.900]
von Willebrand Disease, Type 1 [C15.378.100.100.900.100]
von Willebrand Disease, Type 2 [C15.378.100.100.900.200]
von Willebrand Disease, Type 3 [C15.378.100.100.900.300]
Wiskott-Aldrich Syndrome [C15.378.100.100.970]

 
Hemic and Lymphatic Diseases [C15]
   Hematologic Diseases [C15.378]
      Blood Coagulation Disorders [C15.378.100]
         Coagulation Protein Disorders [C15.378.100.141]
Activated Protein C Resistance [C15.378.100.141.036]
Afibrinogenemia [C15.378.100.141.072]
Factor V Deficiency [C15.378.100.141.300]
Factor VII Deficiency [C15.378.100.141.310]
Factor X Deficiency [C15.378.100.141.320]
Factor XI Deficiency [C15.378.100.141.325]
Factor XII Deficiency [C15.378.100.141.330]
Factor XIII Deficiency [C15.378.100.141.335]
Hemophilia A [C15.378.100.141.500]
Hemophilia B [C15.378.100.141.510]
Hypoprothrombinemias [C15.378.100.141.550]
Arrow pointing to current tree nodevon Willebrand Diseases [C15.378.100.141.900]
von Willebrand Disease, Type 1 [C15.378.100.141.900.100]
von Willebrand Disease, Type 2 [C15.378.100.141.900.200]
von Willebrand Disease, Type 3 [C15.378.100.141.900.300]

 
Hemic and Lymphatic Diseases [C15]
   Hematologic Diseases [C15.378]
      Blood Platelet Disorders [C15.378.140]
Bernard-Soulier Syndrome [C15.378.140.120]
Gray Platelet Syndrome [C15.378.140.427]
Platelet Storage Pool Deficiency [C15.378.140.735]  +
Thrombasthenia [C15.378.140.810]
Thrombocytopenia [C15.378.140.855]  +
Thrombocytosis [C15.378.140.860]  +
Arrow pointing to current tree nodevon Willebrand Diseases [C15.378.140.900]

 
Hemic and Lymphatic Diseases [C15]
   Hematologic Diseases [C15.378]
      Hemorrhagic Disorders [C15.378.463]
Afibrinogenemia [C15.378.463.067]
Bernard-Soulier Syndrome [C15.378.463.080]
Disseminated Intravascular Coagulation [C15.378.463.250]
Factor V Deficiency [C15.378.463.300]
Factor VII Deficiency [C15.378.463.310]
Factor X Deficiency [C15.378.463.320]
Factor XI Deficiency [C15.378.463.325]
Factor XII Deficiency [C15.378.463.330]
Factor XIII Deficiency [C15.378.463.335]
Hemophilia A [C15.378.463.500]
Hemophilia B [C15.378.463.510]
Hemostatic Disorders [C15.378.463.515]  +
Hypoprothrombinemias [C15.378.463.550]
Platelet Storage Pool Deficiency [C15.378.463.735]  +
Purpura, Thrombocytopenic, Idiopathic [C15.378.463.740]
Thrombasthenia [C15.378.463.810]
Thrombocythemia, Essential [C15.378.463.825]
Vitamin K Deficiency [C15.378.463.841]  +
Arrow pointing to current tree nodevon Willebrand Diseases [C15.378.463.920]
von Willebrand Disease, Type 1 [C15.378.463.920.100]
von Willebrand Disease, Type 2 [C15.378.463.920.200]
von Willebrand Disease, Type 3 [C15.378.463.920.300]
Waterhouse-Friderichsen Syndrome [C15.378.463.950]
Wiskott-Aldrich Syndrome [C15.378.463.960]

 
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
   Genetic Diseases, Inborn [C16.320]
      Blood Coagulation Disorders, Inherited [C16.320.099]
Activated Protein C Resistance [C16.320.099.037]
Afibrinogenemia [C16.320.099.056]
Antithrombin III Deficiency [C16.320.099.075]
Bernard-Soulier Syndrome [C16.320.099.080]
Factor V Deficiency [C16.320.099.300]
Factor VII Deficiency [C16.320.099.310]
Factor X Deficiency [C16.320.099.320]
Factor XI Deficiency [C16.320.099.325]
Factor XII Deficiency [C16.320.099.330]
Factor XIII Deficiency [C16.320.099.335]
Gray Platelet Syndrome [C16.320.099.417]
Hemophilia A [C16.320.099.500]
Hemophilia B [C16.320.099.510]
Hermanski-Pudlak Syndrome [C16.320.099.515]
Hypoprothrombinemias [C16.320.099.550]
Protein C Deficiency [C16.320.099.690]
Thrombasthenia [C16.320.099.820]
Arrow pointing to current tree nodevon Willebrand Diseases [C16.320.099.920]
von Willebrand Disease, Type 1 [C16.320.099.920.100]
von Willebrand Disease, Type 2 [C16.320.099.920.200]
von Willebrand Disease, Type 3 [C16.320.099.920.300]
Wiskott-Aldrich Syndrome [C16.320.099.970]

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