ONKI3 | Medical Subject Headings

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Antithrombin III Deficiency

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Blood Coagulation Disorders, Inherited ∟ Antithrombin III Deficiency 25 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Bernard-Soulier Syndrome \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hermanski-Pudlak Syndrome \| ∟ Hypoprothrombinemias \| ∟ Protein C Deficiency \| ∟ Thrombasthenia \| ∟ von Willebrand Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ Agammaglobulinemia \| ∟ Dysgammaglobulinemia \| ∟ Hypergammaglobulinemia \| ∟ Hypoproteinemia \| ∟ Paraproteinemias \| ∟ Protein S Deficiency \| ∟ Disseminated Intravascular Coagulation \| ∟ Purpura, Thrombotic Thrombocytopenic Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Blood Coagulation Disorders, Inherited ∟ Antithrombin III Deficiency 25 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Bernard-Soulier Syndrome \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hermanski-Pudlak Syndrome \| ∟ Hypoprothrombinemias \| ∟ Protein C Deficiency \| ∟ Thrombasthenia \| ∟ von Willebrand Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ Agammaglobulinemia \| ∟ Dysgammaglobulinemia \| ∟ Hypergammaglobulinemia \| ∟ Hypoproteinemia \| ∟ Paraproteinemias \| ∟ Protein S Deficiency \| ∟ Disseminated Intravascular Coagulation \| ∟ Purpura, Thrombotic Thrombocytopenic Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Protein Disorders ∟ Antithrombin III Deficiency 25 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Bernard-Soulier Syndrome \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hermanski-Pudlak Syndrome \| ∟ Hypoprothrombinemias \| ∟ Protein C Deficiency \| ∟ Thrombasthenia \| ∟ von Willebrand Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ Agammaglobulinemia \| ∟ Dysgammaglobulinemia \| ∟ Hypergammaglobulinemia \| ∟ Hypoproteinemia \| ∟ Paraproteinemias \| ∟ Protein S Deficiency \| ∟ Disseminated Intravascular Coagulation \| ∟ Purpura, Thrombotic Thrombocytopenic Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Thrombophilia ∟ Antithrombin III Deficiency 25 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Bernard-Soulier Syndrome \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hermanski-Pudlak Syndrome \| ∟ Hypoprothrombinemias \| ∟ Protein C Deficiency \| ∟ Thrombasthenia \| ∟ von Willebrand Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ Agammaglobulinemia \| ∟ Dysgammaglobulinemia \| ∟ Hypergammaglobulinemia \| ∟ Hypoproteinemia \| ∟ Paraproteinemias \| ∟ Protein S Deficiency \| ∟ Disseminated Intravascular Coagulation \| ∟ Purpura, Thrombotic Thrombocytopenic X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Blood Coagulation Disorders, Inherited ∟ Antithrombin III Deficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Blood Coagulation Disorders, Inherited ∟ Antithrombin III Deficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Protein Disorders ∟ Antithrombin III Deficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Thrombophilia ∟ Antithrombin III Deficiency 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 Protein Disorders > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) Thrombophilia > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) X
History note:	Antithrombin III/deficiency (1979-1998) \| Antithrombins/deficiency (1971-1978)X
historyNote*:	99 X
publicMeSHNote*:	99 X
Scope note:	An absence or reduced level of Antithrombin III leading to an increased risk for thrombosis. X
activeMeSHYear*:	2007X
dateCreated*:	1998-06-18X
dateEstablished*:	1999-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	agsX
recordOriginator*:	NNSX
Type:	Concept X
Coordinate terms:	Activated Protein C Resistance \| Afibrinogenemia \| Bernard-Soulier Syndrome \| Factor V Deficiency \| Factor VII Deficiency \| Factor X Deficiency \| Factor XI Deficiency \| Factor XII Deficiency \| Factor XIII Deficiency \| Hemophilia A \| Hemophilia B \| Hermanski-Pudlak Syndrome \| Hypoprothrombinemias \| Protein C Deficiency \| Thrombasthenia \| von Willebrand Disease \| Wiskott-Aldrich Syndrome \| Agammaglobulinemia \| Dysgammaglobulinemia \| Hypergammaglobulinemia \| Hypoproteinemia \| Paraproteinemias \| Protein S Deficiency \| Disseminated Intravascular Coagulation \| Purpura, Thrombotic Thrombocytopenic X
URI:	X
Labels and equivalent concepts:	Antitrombiini III:n puutos (fi) AT III:n puutos (fi, replaced) AT III:n puute (fi, replaced) Antitrombiini III:n puute (fi, replaced) Antitrombin III-brist (sv) Deficiency, Antithrombin III (en, replaced) Antithrombin 3 Deficiency (en, replaced) X
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