Concept information
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Blood Coagulation Disorders, Inherited
Preferred term
von Willebrand Diseases
Type
-
Topical Descriptor
Broader concept
Narrower concepts
Entry terms
- Angiohemophilia
- Angiohemophilias
- Disorder, Von Willebrand
- Hemophilia, Vascular
- Pseudohemophilias, Vascular
- Pseudohemophilia, Vascular
- Vascular Hemophilia
- Vascular Hemophilias
- Vascular Pseudohemophilia
- Vascular Pseudohemophilias
- von Willebrand Disease
- Von Willebrand Disorder
- von Willebrand's Disease
- von Willebrand's Diseases
- Von Willebrand's Factor Deficiency
Note
- note specific types of Von Willebrand Disease are available
Scope note
- Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion.
History note
- 2010(1963)
In other languages
-
Finnish
-
angiohaemophilia
-
angiohemofili
-
angiohemofilia
-
deficientia factoris VIII cum defectu endotheliali
-
faktor VIII-brist med vaskulär defekt
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haemophilia vascularis
-
hyytymistekijä VIII:n puute
-
morbus von Willebrand
-
vaskulaarinen hemofilia
-
vaskulär hemofili
-
verisuonten endoteelivajaukseen liittyvä tekijä VIII:n puute
-
von Willebrand
-
von Willebrandin taudit
-
von Willebrands sjukdom
-
von Willebrandt
-
von Willebrandtin tauti
-
von Willebrant
-
von Willebrantin tauti
-
Willebrand
-
Willebrandt
-
Willebrant
-
Swedish
-
Angiohemofili
-
Vaskulär hemofili
-
Vaskulär pseudohemofili
-
Willebrands sjukdomar
URI
http://www.yso.fi/onto/mesh/D014842
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