ONKI3 | Medical Subject Headings

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Bernard-Soulier Syndrome

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Blood Coagulation Disorders, Inherited ∟ Bernard-Soulier Syndrome 26 coordinate concepts ∟ Platelet Storage Pool Deficiency \| ∟ Thrombasthenia \| ∟ Thrombocytopenia \| ∟ Thrombocytosis \| ∟ von Willebrand Disease \| ∟ Afibrinogenemia \| ∟ Disseminated Intravascular Coagulation \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombocythemia, Hemorrhagic \| ∟ Vascular Hemostatic Disorders \| ∟ Vitamin K Deficiency \| ∟ Waterhouse-Friderichsen Syndrome \| ∟ Wiskott-Aldrich Syndrome \| ∟ Activated Protein C Resistance \| ∟ 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 ∟ Bernard-Soulier Syndrome 26 coordinate concepts ∟ Platelet Storage Pool Deficiency \| ∟ Thrombasthenia \| ∟ Thrombocytopenia \| ∟ Thrombocytosis \| ∟ von Willebrand Disease \| ∟ Afibrinogenemia \| ∟ Disseminated Intravascular Coagulation \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombocythemia, Hemorrhagic \| ∟ Vascular Hemostatic Disorders \| ∟ Vitamin K Deficiency \| ∟ Waterhouse-Friderichsen Syndrome \| ∟ Wiskott-Aldrich Syndrome \| ∟ Activated Protein C Resistance \| ∟ Antithrombin III Deficiency \| ∟ Hermanski-Pudlak Syndrome \| ∟ Protein C Deficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Platelet Disorders ∟ Bernard-Soulier Syndrome 26 coordinate concepts ∟ Platelet Storage Pool Deficiency \| ∟ Thrombasthenia \| ∟ Thrombocytopenia \| ∟ Thrombocytosis \| ∟ von Willebrand Disease \| ∟ Afibrinogenemia \| ∟ Disseminated Intravascular Coagulation \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombocythemia, Hemorrhagic \| ∟ Vascular Hemostatic Disorders \| ∟ Vitamin K Deficiency \| ∟ Waterhouse-Friderichsen Syndrome \| ∟ Wiskott-Aldrich Syndrome \| ∟ Activated Protein C Resistance \| ∟ Antithrombin III Deficiency \| ∟ Hermanski-Pudlak Syndrome \| ∟ Protein C Deficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Hemorrhagic Disorders ∟ Bernard-Soulier Syndrome 26 coordinate concepts ∟ Platelet Storage Pool Deficiency \| ∟ Thrombasthenia \| ∟ Thrombocytopenia \| ∟ Thrombocytosis \| ∟ von Willebrand Disease \| ∟ Afibrinogenemia \| ∟ Disseminated Intravascular Coagulation \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombocythemia, Hemorrhagic \| ∟ Vascular Hemostatic Disorders \| ∟ Vitamin K Deficiency \| ∟ Waterhouse-Friderichsen Syndrome \| ∟ Wiskott-Aldrich Syndrome \| ∟ Activated Protein C Resistance \| ∟ 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 ∟ Bernard-Soulier Syndrome Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Blood Coagulation Disorders, Inherited ∟ Bernard-Soulier Syndrome Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Platelet Disorders ∟ Bernard-Soulier Syndrome Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Hemorrhagic Disorders ∟ Bernard-Soulier Syndrome 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) 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:	a familial blood platelet disord X
History note:	Blood Platelet Disorders (1967-1985)X
historyNote*:	91(86); was see under BLOOD PLATELET DISORDERS 1986-90 X
publicMeSHNote*:	91; was see under BLOOD PLATELET DISORDERS 1986-90 X
Scope note:	A familial coagulation disorder characterized by a prolonged bleeding time, unusually large platelets, and impaired prothrombin consumption. X
activeMeSHYear*:	2007X
dateCreated*:	1985-03-11X
dateEstablished*:	1991-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	agsX
recordOriginator*:	VDKX
Type:	Concept X
Coordinate terms:	Platelet Storage Pool Deficiency \| Thrombasthenia \| Thrombocytopenia \| Thrombocytosis \| von Willebrand Disease \| Afibrinogenemia \| Disseminated Intravascular Coagulation \| Factor V Deficiency \| Factor VII Deficiency \| Factor X Deficiency \| Factor XI Deficiency \| Factor XII Deficiency \| Factor XIII Deficiency \| Hemophilia A \| Hemophilia B \| Hypoprothrombinemias \| Purpura, Thrombocytopenic, Idiopathic \| Thrombocythemia, Hemorrhagic \| Vascular Hemostatic Disorders \| Vitamin K Deficiency \| Waterhouse-Friderichsen Syndrome \| Wiskott-Aldrich Syndrome \| Activated Protein C Resistance \| Antithrombin III Deficiency \| Hermanski-Pudlak Syndrome \| Protein C Deficiency X
URI:	X
Labels and equivalent concepts:	Bernard-Soulierin oireyhtymä (fi) Jättitrombosyyttisyndrooma (fi, replaced) Jättitrombosyyttioireyhtymä (fi, replaced) Bernard-Soulierin syndrooma (fi, replaced) Bernard-Souliers syndrom (sv) Giant Platelet Syndrome (en, replaced) Syndroma Bernard-Soulier (la-FI, replaced) X
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