ONKI3 | Medical Subject Headings

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The way property values are displayed: value/row values side by side

The way concept relations are shown: separately in hierarchy

von Willebrand Disease

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Blood Coagulation Disorders, Inherited ∟ von Willebrand Disease 26 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Bernard-Soulier Syndrome \| ∟ Platelet Storage Pool Deficiency \| ∟ Thrombasthenia \| ∟ Thrombocytopenia \| ∟ Thrombocytosis \| ∟ Disseminated Intravascular Coagulation \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombocythemia, Hemorrhagic \| ∟ Vascular Hemostatic Disorders \| ∟ Vitamin K Deficiency \| ∟ Waterhouse-Friderichsen Syndrome \| ∟ Wiskott-Aldrich Syndrome \| ∟ Antithrombin III Deficiency \| ∟ Hermanski-Pudlak Syndrome \| ∟ Protein C Deficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Blood Coagulation Disorders, Inherited ∟ von Willebrand Disease 26 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Bernard-Soulier Syndrome \| ∟ Platelet Storage Pool Deficiency \| ∟ Thrombasthenia \| ∟ Thrombocytopenia \| ∟ Thrombocytosis \| ∟ Disseminated Intravascular Coagulation \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombocythemia, Hemorrhagic \| ∟ Vascular Hemostatic Disorders \| ∟ Vitamin K Deficiency \| ∟ Waterhouse-Friderichsen Syndrome \| ∟ Wiskott-Aldrich Syndrome \| ∟ Antithrombin III Deficiency \| ∟ Hermanski-Pudlak Syndrome \| ∟ Protein C Deficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Coagulation Protein Disorders ∟ von Willebrand Disease 26 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Bernard-Soulier Syndrome \| ∟ Platelet Storage Pool Deficiency \| ∟ Thrombasthenia \| ∟ Thrombocytopenia \| ∟ Thrombocytosis \| ∟ Disseminated Intravascular Coagulation \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombocythemia, Hemorrhagic \| ∟ Vascular Hemostatic Disorders \| ∟ Vitamin K Deficiency \| ∟ Waterhouse-Friderichsen Syndrome \| ∟ Wiskott-Aldrich Syndrome \| ∟ Antithrombin III Deficiency \| ∟ Hermanski-Pudlak Syndrome \| ∟ Protein C Deficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Platelet Disorders ∟ von Willebrand Disease 26 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Bernard-Soulier Syndrome \| ∟ Platelet Storage Pool Deficiency \| ∟ Thrombasthenia \| ∟ Thrombocytopenia \| ∟ Thrombocytosis \| ∟ Disseminated Intravascular Coagulation \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombocythemia, Hemorrhagic \| ∟ Vascular Hemostatic Disorders \| ∟ Vitamin K Deficiency \| ∟ Waterhouse-Friderichsen Syndrome \| ∟ Wiskott-Aldrich Syndrome \| ∟ Antithrombin III Deficiency \| ∟ Hermanski-Pudlak Syndrome \| ∟ Protein C Deficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Hemorrhagic Disorders ∟ von Willebrand Disease 26 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Bernard-Soulier Syndrome \| ∟ Platelet Storage Pool Deficiency \| ∟ Thrombasthenia \| ∟ Thrombocytopenia \| ∟ Thrombocytosis \| ∟ Disseminated Intravascular Coagulation \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombocythemia, Hemorrhagic \| ∟ Vascular Hemostatic Disorders \| ∟ Vitamin K Deficiency \| ∟ Waterhouse-Friderichsen Syndrome \| ∟ Wiskott-Aldrich Syndrome \| ∟ Antithrombin III Deficiency \| ∟ Hermanski-Pudlak Syndrome \| ∟ Protein C Deficiency X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Blood Coagulation Disorders, Inherited ∟ von Willebrand Disease Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Blood Coagulation Disorders, Inherited ∟ von Willebrand Disease Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Coagulation Protein Disorders ∟ von Willebrand Disease Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Platelet Disorders ∟ von Willebrand Disease Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Hemorrhagic Disorders ∟ von Willebrand Disease Blood Coagulation Disorders, Inherited > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Blood Coagulation Disorders, Inherited > Blood Coagulation Disorders > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) Coagulation Protein Disorders > Blood Coagulation Disorders > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) Blood Platelet Disorders > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) Hemorrhagic Disorders > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) X
Annotation:	do not coord with INFANT, NEWBORN, DISEASES X
historyNote*:	99(63) X
publicMeSHNote*:	99; see von Willebrand's Disease 1968-98, see HEMORRHAGIC DIATHESIS 1967, see THROMBOCYTOPATHY 1963-66 X
Scope note:	Group of hemorrhagic disorders in which the von Willebrand factor (Factor VIII-related antigen) 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. X
activeMeSHYear*:	2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1968-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	agsX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Activated Protein C Resistance \| Afibrinogenemia \| Factor V Deficiency \| Factor VII Deficiency \| Factor X Deficiency \| Factor XI Deficiency \| Factor XII Deficiency \| Factor XIII Deficiency \| Hemophilia A \| Hemophilia B \| Hypoprothrombinemias \| Bernard-Soulier Syndrome \| Platelet Storage Pool Deficiency \| Thrombasthenia \| Thrombocytopenia \| Thrombocytosis \| Disseminated Intravascular Coagulation \| Purpura, Thrombocytopenic, Idiopathic \| Thrombocythemia, Hemorrhagic \| Vascular Hemostatic Disorders \| Vitamin K Deficiency \| Waterhouse-Friderichsen Syndrome \| Wiskott-Aldrich Syndrome \| Antithrombin III Deficiency \| Hermanski-Pudlak Syndrome \| Protein C Deficiency X
URI:	X
Labels and equivalent concepts:	von Willebrandin tauti (fi) Vaskulaarinen hemofilia (fi, replaced) Angiohemofilia (fi, replaced) von Willebrands sjukdom (sv) Willebrands sjukdom (sv, replaced) Hemophilia, Vascular (en, replaced) von Willebrand's Disease (en, replaced) Angiohemophilia (en, replaced) Morbus von Willebrand (la-FI, replaced) X
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