ONKI3 | Medical Subject Headings

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Factor XII Deficiency

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Blood Coagulation Disorders, Inherited ∟ Factor XII Deficiency 24 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ von Willebrand Disease \| ∟ Bernard-Soulier Syndrome \| ∟ Disseminated Intravascular Coagulation \| ∟ Platelet Storage Pool Deficiency \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombasthenia \| ∟ 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 ∟ Factor XII Deficiency 24 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ von Willebrand Disease \| ∟ Bernard-Soulier Syndrome \| ∟ Disseminated Intravascular Coagulation \| ∟ Platelet Storage Pool Deficiency \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombasthenia \| ∟ 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 ∟ Factor XII Deficiency 24 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ von Willebrand Disease \| ∟ Bernard-Soulier Syndrome \| ∟ Disseminated Intravascular Coagulation \| ∟ Platelet Storage Pool Deficiency \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombasthenia \| ∟ 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 ∟ Factor XII Deficiency 24 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ von Willebrand Disease \| ∟ Bernard-Soulier Syndrome \| ∟ Disseminated Intravascular Coagulation \| ∟ Platelet Storage Pool Deficiency \| ∟ Purpura, Thrombocytopenic, Idiopathic \| ∟ Thrombasthenia \| ∟ 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 ∟ Factor XII Deficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Blood Coagulation Disorders, Inherited ∟ Factor XII Deficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Coagulation Protein Disorders ∟ Factor XII Deficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Hemorrhagic Disorders ∟ Factor XII 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) Coagulation Protein Disorders > Blood Coagulation 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 blood coag disord; DF: FACTOR XII DEFIC X
History note:	Blood Coagulation Disorders (1966-1977) \| Factor XII (1966-1977)X
historyNote*:	78 X
publicMeSHNote*:	78 X
Scope note:	An absence or reduced level of blood coagulation factor XII. It normally occurs in the absence of patient or family history of hemorrhagic disorders and is marked by prolonged clotting time. X
activeMeSHYear*:	2007X
dateCreated*:	1977-04-27X
dateEstablished*:	1978-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	agsX
recordOriginator*:	VDKX
Type:	Concept X
Coordinate terms:	Activated Protein C Resistance \| Afibrinogenemia \| Factor V Deficiency \| Factor VII Deficiency \| Factor X Deficiency \| Factor XI Deficiency \| Factor XIII Deficiency \| Hemophilia A \| Hemophilia B \| Hypoprothrombinemias \| von Willebrand Disease \| Bernard-Soulier Syndrome \| Disseminated Intravascular Coagulation \| Platelet Storage Pool Deficiency \| Purpura, Thrombocytopenic, Idiopathic \| Thrombasthenia \| 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:	Hageman-tekijän puutos (fi) Hyytymistekijän XII puutos (fi, replaced) Hyytymistekijän XII puute (fi, replaced) Tekijä XII:n puute (fi, replaced) Tekijä XII:n puutos (fi, replaced) Tekijän XII puutos (fi, replaced) Tekijän XII puute (fi, replaced) Hyytymistekijä XII:n puutos (fi, replaced) Hyytymistekijä XII:n puute (fi, replaced) Faktori XII:n puute (fi, replaced) Faktori XII:n puutos (fi, replaced) Faktorin XII puute (fi, replaced) Hageman-tekijän puute (fi, replaced) Faktorin XII puutos (fi, replaced) Faktor XII-brist (sv) Hageman Trait (en, replaced) Deficiency, Factor XII (en, replaced) X
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