ONKI3 | Medical Subject Headings

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Protein C Deficiency

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Blood Coagulation Disorders, Inherited ∟ Protein C Deficiency 25 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Antithrombin III Deficiency \| ∟ 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 \| ∟ 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 ∟ Protein C Deficiency 25 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Antithrombin III Deficiency \| ∟ 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 \| ∟ 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 ∟ Protein C Deficiency 25 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Antithrombin III Deficiency \| ∟ 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 \| ∟ 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 ∟ Protein C Deficiency 25 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Antithrombin III Deficiency \| ∟ 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 \| ∟ 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 ∟ Protein C Deficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Blood Coagulation Disorders, Inherited ∟ Protein C Deficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Protein Disorders ∟ Protein C Deficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Thrombophilia ∟ Protein C 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
Annotation:	DF: PROTEIN C DEFIC X
History note:	Blood Proteins (1981-1987) \| Glycoproteins (1981-1987) \| Protein C (1987-1998)X
historyNote*:	99 X
publicMeSHNote*:	99 X
Scope note:	An absence or deficiency in PROTEIN C which leads to impaired regulation of blood coagulation. It is associated with an increased risk of severe or premature thrombosis. (Stedman's Med. Dict., 26th ed.) X
activeMeSHYear*:	2007X
dateCreated*:	1998-06-10X
dateEstablished*:	1999-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	agsX
recordOriginator*:	NNSX
Related term:	Activated Protein C Resistance X
Type:	Concept X
Coordinate terms:	Activated Protein C Resistance \| Afibrinogenemia \| Antithrombin III Deficiency \| 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 \| 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:	Proteiini C:n puutos (fi) Proteiini C:n puute (fi, replaced) C-proteiinin puutos (fi, replaced) C-proteiinin puute (fi, replaced) Protein C-brist (sv) Deficiency, Protein C (en, replaced) X
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