ONKI3 | Medical Subject Headings

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Activated Protein C Resistance

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Blood Coagulation Disorders, Inherited ∟ Activated Protein C Resistance 20 coordinate concepts ∟ Afibrinogenemia \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ von Willebrand Disease \| ∟ Antithrombin III Deficiency \| ∟ Bernard-Soulier Syndrome \| ∟ Hermanski-Pudlak Syndrome \| ∟ Protein C Deficiency \| ∟ Thrombasthenia \| ∟ Wiskott-Aldrich Syndrome \| ∟ Disseminated Intravascular Coagulation \| ∟ Protein S Deficiency \| ∟ Purpura, Thrombotic Thrombocytopenic Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Blood Coagulation Disorders, Inherited ∟ Activated Protein C Resistance 20 coordinate concepts ∟ Afibrinogenemia \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ von Willebrand Disease \| ∟ Antithrombin III Deficiency \| ∟ Bernard-Soulier Syndrome \| ∟ Hermanski-Pudlak Syndrome \| ∟ Protein C Deficiency \| ∟ Thrombasthenia \| ∟ Wiskott-Aldrich Syndrome \| ∟ Disseminated Intravascular Coagulation \| ∟ Protein S Deficiency \| ∟ Purpura, Thrombotic Thrombocytopenic Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Coagulation Protein Disorders ∟ Activated Protein C Resistance 20 coordinate concepts ∟ Afibrinogenemia \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ von Willebrand Disease \| ∟ Antithrombin III Deficiency \| ∟ Bernard-Soulier Syndrome \| ∟ Hermanski-Pudlak Syndrome \| ∟ Protein C Deficiency \| ∟ Thrombasthenia \| ∟ Wiskott-Aldrich Syndrome \| ∟ Disseminated Intravascular Coagulation \| ∟ Protein S Deficiency \| ∟ Purpura, Thrombotic Thrombocytopenic Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Thrombophilia ∟ Activated Protein C Resistance 20 coordinate concepts ∟ Afibrinogenemia \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ von Willebrand Disease \| ∟ Antithrombin III Deficiency \| ∟ Bernard-Soulier Syndrome \| ∟ Hermanski-Pudlak Syndrome \| ∟ Protein C Deficiency \| ∟ Thrombasthenia \| ∟ Wiskott-Aldrich Syndrome \| ∟ Disseminated Intravascular Coagulation \| ∟ Protein S Deficiency \| ∟ Purpura, Thrombotic Thrombocytopenic X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Blood Coagulation Disorders, Inherited ∟ Activated Protein C Resistance Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Blood Coagulation Disorders, Inherited ∟ Activated Protein C Resistance Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Coagulation Protein Disorders ∟ Activated Protein C Resistance Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Thrombophilia ∟ Activated Protein C Resistance 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) Thrombophilia > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) X
History note:	Factor V/genetics (1994-1998) \| Protein C (1993-1998)X
historyNote*:	99 X
publicMeSHNote*:	99 X
Scope note:	A hemostatic disorder characterized by a poor anticoagulant response to activated protein C (APC). The activated form of Factor V (Factor Va) is more slowly degraded by activated protein C. Factor V Leiden mutation (R506Q) is the most common cause of APC resistance. X
activeMeSHYear*:	2007X
dateCreated*:	1998-06-10X
dateEstablished*:	1999-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	agsX
recordOriginator*:	NNSX
Related term:	Protein C Deficiency X
Type:	Concept X
Coordinate terms:	Afibrinogenemia \| Factor V Deficiency \| Factor VII Deficiency \| Factor X Deficiency \| Factor XI Deficiency \| Factor XII Deficiency \| Factor XIII Deficiency \| Hemophilia A \| Hemophilia B \| Hypoprothrombinemias \| von Willebrand Disease \| Antithrombin III Deficiency \| Bernard-Soulier Syndrome \| Hermanski-Pudlak Syndrome \| Protein C Deficiency \| Thrombasthenia \| Wiskott-Aldrich Syndrome \| Disseminated Intravascular Coagulation \| Protein S Deficiency \| Purpura, Thrombotic Thrombocytopenic X
URI:	X
Labels and equivalent concepts:	APC-resistenssi (fi) Resistenssi aktivoituneelle proteiini C:lle (fi, replaced) Resistenssi aktivoituneelle proteiini-C:lle (fi, replaced) Resistenssi aktivoidulle proteiini-C:lle (fi, replaced) Resistenssi aktivoidulle proteiini C:lle (fi, replaced) Aktivoidun proteiini-C:n resistenssi (fi, replaced) FV-mutaatio (fi, replaced) Hyytymistekijä V:n mutaatio (fi, replaced) Aktiverat protein C-resistens (sv) APC-resistens (sv, replaced) APC Resistance (en, replaced) X
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