ONKI3 | Medical Subject Headings


Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Blood Coagulation Disorders, Inherited ∟ Thrombasthenia 26 coordinate concepts ∟ Bernard-Soulier Syndrome \| ∟ Platelet Storage Pool Deficiency \| ∟ 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 ∟ Thrombasthenia 26 coordinate concepts ∟ Bernard-Soulier Syndrome \| ∟ Platelet Storage Pool Deficiency \| ∟ 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 ∟ Thrombasthenia 26 coordinate concepts ∟ Bernard-Soulier Syndrome \| ∟ Platelet Storage Pool Deficiency \| ∟ 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 ∟ Thrombasthenia 26 coordinate concepts ∟ Bernard-Soulier Syndrome \| ∟ Platelet Storage Pool Deficiency \| ∟ 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 ∟ Thrombasthenia Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Blood Coagulation Disorders, Inherited ∟ Thrombasthenia Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Platelet Disorders ∟ Thrombasthenia Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Hemorrhagic Disorders ∟ Thrombasthenia 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
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 congenital bleeding disorder with prolonged bleeding time, absence of aggregation of platelets in response to most agents, especially ADP, and impaired or absent clot retraction. Platelet membranes are deficient in or have a defect in the glycoprotein IIb-IIIa complex (PLATELET GLYCOPROTEIN GPIIB-IIIA COMPLEX). X
activeMeSHYear*:	2007X
dateCreated*:	1985-03-11X
dateEstablished*:	1991-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	agsX
recordOriginator*:	VDKX
Related term:	Platelet Glycoprotein GPIIb-IIIa Complex X
Type:	Concept X
Coordinate terms:	Bernard-Soulier Syndrome \| Platelet Storage Pool Deficiency \| 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:	Trombastenia (fi) Glantzmannin tauti (fi, replaced) Glantzmannin sairaus (fi, replaced) Glanzmann Thrombasthenia (en, replaced) Thrombasthenia (la-FI, replaced) Morbus Glantzmann (la-FI, replaced) X
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