ONKI3 | Medical Subject Headings

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

The way concept relations are shown: separately in hierarchy

Blood Coagulation Disorders, Inherited

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Blood Coagulation Disorders, Inherited 42 coordinate concepts 18 subordinate 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 \| ∟ Protein C Deficiency \| ∟ Thrombasthenia \| ∟ von Willebrand Disease \| ∟ Wiskott-Aldrich Syndrome ∟ Coagulation Protein Disorders \| ∟ Disseminated Intravascular Coagulation \| ∟ Platelet Storage Pool Deficiency \| ∟ Protein S Deficiency \| ∟ Purpura \| ∟ Purpura, Thrombocytopenic \| ∟ Thrombocythemia, Hemorrhagic \| ∟ Vitamin K Deficiency \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Brugada Syndrome \| ∟ CADASIL \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Blood Coagulation Disorders, Inherited 42 coordinate concepts 18 subordinate 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 \| ∟ Protein C Deficiency \| ∟ Thrombasthenia \| ∟ von Willebrand Disease \| ∟ Wiskott-Aldrich Syndrome ∟ Coagulation Protein Disorders \| ∟ Disseminated Intravascular Coagulation \| ∟ Platelet Storage Pool Deficiency \| ∟ Protein S Deficiency \| ∟ Purpura \| ∟ Purpura, Thrombocytopenic \| ∟ Thrombocythemia, Hemorrhagic \| ∟ Vitamin K Deficiency \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Brugada Syndrome \| ∟ CADASIL \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Blood Coagulation Disorders, Inherited Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Blood Coagulation Disorders, Inherited Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Blood Coagulation Disorders > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) X
Narrower 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 \| Protein C Deficiency \| Thrombasthenia \| von Willebrand Disease \| Wiskott-Aldrich Syndrome X
History note:	Blood Coagulation Disorders (1995-2001)X
historyNote*:	2002 X
publicMeSHNote*:	2002 X
Scope note:	Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation. X
activeMeSHYear*:	2007X
dateCreated*:	2001-07-25X
dateEstablished*:	2002-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	agsX
recordOriginator*:	nnsX
Type:	Concept X
Coordinate terms:	Coagulation Protein Disorders \| Disseminated Intravascular Coagulation \| Platelet Storage Pool Deficiency \| Protein S Deficiency \| Purpura \| Purpura, Thrombocytopenic \| Thrombocythemia, Hemorrhagic \| Vitamin K Deficiency \| Adrenal Hyperplasia, Congenital \| Anemia, Hemolytic, Congenital \| Anemia, Hypoplastic, Congenital \| Ataxia Telangiectasia \| Brugada Syndrome \| CADASIL \| Camurati-Engelmann Syndrome \| Cardiomyopathy, Hypertrophic, Familial \| Cherubism \| Chromosome Disorders \| Cystic Fibrosis \| Dwarfism \| Eye Diseases, Hereditary \| Familial Mediterranean Fever \| Genetic Diseases, X-Linked \| Genetic Diseases, Y-Linked \| Hajdu-Cheney Syndrome \| Hemoglobinopathies \| Heredodegenerative Disorders, Nervous System \| Hyperthyroxinemia, Familial Dysalbuminemic \| Jervell-Lange Nielsen Syndrome \| Kallmann Syndrome \| Kartagener Syndrome \| Marfan Syndrome \| Metabolism, Inborn Errors \| Muscular Dystrophies \| Myasthenic Syndromes, Congenital \| Nail-Patella Syndrome \| Neoplastic Syndromes, Hereditary \| Osteogenesis Imperfecta \| Pain Insensitivity, Congenital \| Romano-Ward Syndrome \| Skin Diseases, Genetic \| Werner Syndrome X
URI:	X
Labels and equivalent concepts:	Perinnölliset hyytymishäiriöt (fi) Perinnöllinen hyytymishäiriö (fi, replaced) Perinnöllinen koagulopatia (fi, replaced) Perinnölliset koagulopatiat (fi, replaced) Blodkoagulationsstörningar, ärftliga (sv) Inherited Coagulation Disorders (en, replaced) Inherited Blood Coagulation Disorders (en, replaced) Hereditary Blood Coagulation Disorders (en, replaced) Hereditary Coagulation Disorders (en, replaced) Coagulation Disorders, Inherited (en, replaced) X
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