Concept information
Preferred term
Blood Coagulation Disorders, Inherited
Type
-
Topical Descriptor
Broader concept
Narrower 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
- Gray Platelet Syndrome
- Hemophilia A
- Hemophilia B
- Hermanski-Pudlak Syndrome
- Hypoprothrombinemias
- Protein C Deficiency
- Thrombasthenia
- von Willebrand Diseases
- Wiskott-Aldrich Syndrome
Entry terms
- Coagulation Disorder, Hereditary
- Coagulation Disorder, Inherited
- Coagulation Disorders, Hereditary
- Coagulation Disorders, Inherited
- Hereditary Blood Coagulation Disorders
- Hereditary Coagulation Disorder
- Hereditary Coagulation Disorders
- Inherited Blood Coagulation Disorders
- Inherited Coagulation Disorder
- Inherited Coagulation Disorders
Scope note
- Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation.
History note
- 2002
In other languages
-
Finnish
-
perinnöllinen hyytymishäiriö
-
perinnöllinen koagulopatia
-
perinnölliset koagulopatiat
-
Swedish
-
Ärftliga blodkoagulationsstörningar
URI
http://www.yso.fi/onto/mesh/D025861
{{label}}
{{#each values }} {{! loop through ConceptPropertyValue objects }}
{{#if prefLabel }}
{{/if}}
{{/each}}
{{#if notation }}{{ notation }} {{/if}}{{ prefLabel }}
{{#ifDifferentLabelLang lang }} ({{ lang }}){{/ifDifferentLabelLang}}
{{#if vocabName }}
{{ vocabName }}
{{/if}}