ONKI3 | Medical Subject Headings

The ONKI is provided as a part of the ONKI Living Lab - an open lab for testing the latest semantic web technologies in practice, with real users like you. Currently, over 10 000 people are using ONKI each month.

We hope you like the ONKI service and enjoy using it for your purposes!

If you encounter any problems or have improvement ideas, please contact the ONKI team. We are also very much interested in your success stories in using ONKI - please share your experiences!

The ONKI Team

Jouni Tuominen, Living Lab contact person, APIs, widgets, publishing of ontologies, etc.
Eero Hyvönen, professor, head of research group

Former members: Kim Viljanen, Rami Alatalo.

Building the future of the Semantic Web and beyond.

SeCo's homepage
For the latest semantic news, follow us on Twitter and fan us on Facebook!

How can we help you?

Live presentations about ONKI: what it is? how to use it?
Support for creating and publishing ontologies.
Online technical support for using ONKI.
Co-operation in projects.
And more, please ask.

suomeksi på svenska in English

The way property values are displayed: value/row values side by side

The way concept relations are shown: separately in hierarchy

Factor X Deficiency

Loading results...


Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Blood Coagulation Disorders, Inherited ∟ Factor X Deficiency 24 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Factor V Deficiency \| ∟ Factor VII 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 X Deficiency 24 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Factor V Deficiency \| ∟ Factor VII 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 X Deficiency 24 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Factor V Deficiency \| ∟ Factor VII 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 X Deficiency 24 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Factor V Deficiency \| ∟ Factor VII 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 X Deficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Blood Coagulation Disorders, Inherited ∟ Factor X Deficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Coagulation Protein Disorders ∟ Factor X Deficiency Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Hemorrhagic Disorders ∟ Factor X 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 X DEFIC X
historyNote*:	91(75); was see under HYPOPROTHROMBINEMIAS 1975-90 X
onlineNote*:	search HYPOPROTHROMBINEMIAS 1966-74 X
publicMeSHNote*:	91; was see under HYPOPROTHROMBINEMIAS 1975-90 X
Scope note:	Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in both the intrinsic and extrinsic pathways, impaired thromboplastin time, and impaired prothrombin consumption. X
activeMeSHYear*:	2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1991-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	agsX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Activated Protein C Resistance \| Afibrinogenemia \| Factor V Deficiency \| Factor VII 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:	Stuart Powerin tekijän puutos (fi) Hyytymistekijän X puutos (fi, replaced) Hyytymistekijän X puute (fi, replaced) Hyytymistekijä X:n puutos (fi, replaced) Stuart Powerin tekijän puute (fi, replaced) Tekijä X:n puute (fi, replaced) Tekijän X puutos (fi, replaced) Tekijän X puute (fi, replaced) Tekijä X:n puutos (fi, replaced) Hyytymistekijä X:n puute (fi, replaced) Faktorin X puutos (fi, replaced) Faktori X:n puute (fi, replaced) Faktorin X puute (fi, replaced) Faktori X:n puutos (fi, replaced) Faktor X-brist (sv) Stuart-Prower Deficiency (en, replaced) Deficiency, Stuart-Prower Factor (en, replaced) Deficiency, Stuart-Prower (en, replaced) Stuart-Prower Factor Deficiency (en, replaced) Deficiency, Factor X (en, replaced) X
Share:	X