ONKI3 | Medical Subject Headings

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Factor V 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 V Deficiency 24 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII 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 V Deficiency 24 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII 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 V Deficiency 24 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII 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 V Deficiency 24 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII 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 V Deficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Blood Coagulation Disorders, Inherited ∟ Factor V Deficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Coagulation Protein Disorders ∟ Factor V Deficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Hemorrhagic Disorders ∟ Factor V 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 V DEFIC X
historyNote*:	73(64); was see under HYPOPROTHROMBINEMIAS 1963-72 X
onlineNote*:	use HYPOPROTHROMBINEMIAS to search FACTOR V DEFICIENCY 1966-72 X
publicMeSHNote*:	73; was see under HYPOPROTHROMBINEMIAS 1963-72 X
Scope note:	A deficiency of blood coagulation factor V (known as proaccelerin or accelerator globulin or labile factor) leading to a rare hemorrhagic tendency known as Owren's disease or parahemophilia. It varies greatly in severity. Factor V deficiency is an autosomal recessive trait. (Dorland, 27th ed) X
activeMeSHYear*:	2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1973-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	agsX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Activated Protein C Resistance \| Afibrinogenemia \| Factor VII Deficiency \| Factor X Deficiency \| Factor XI Deficiency \| Factor XII 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:	Proakseleriinin puutos (fi) Proakseleriinipuute (fi, replaced) Proakseleriinin puute (fi, replaced) Hyytymistekijän V puutos (fi, replaced) Hyytymistekijän V puute (fi, replaced) Proakseleriinipuutos (fi, replaced) Tekijä V:n puute (fi, replaced) Tekijän V puutos (fi, replaced) Tekijän V puute (fi, replaced) Tekijä V:n puutos (fi, replaced) Hyytymistekijä V:n puutos (fi, replaced) Hyytymistekijä V:n puute (fi, replaced) Faktori V:n puute (fi, replaced) Faktori V:n puutos (fi, replaced) Faktorin V puute (fi, replaced) FV-puutos (fi, replaced) FV-puute (fi, replaced) Faktorin V puutos (fi, replaced) Faktor V-brist (sv) Parahemophilia (en, replaced) Owren's Disease (en, replaced) Owren Disease (en, replaced) Deficiency, Factor V (en, replaced) X
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