Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
von Willebrand Diseases
Preferred term
von Willebrand Disease, Type 2
Type
-
Topical Descriptor
Broader concept
Entry terms
- Type 2 von Willebrand Disease
- Type II von Willebrand Disease
- von Willebrand Disease, Type II
Scope note
- A subtype of von Willebrand disease that results from qualitative deficiencies of VON WILLEBRAND FACTOR. The subtype is divided into several variants with each variant having a distinctive pattern of PLATELET-interaction.
History note
- 2010
In other languages
-
Finnish
-
Swedish
URI
http://www.yso.fi/onto/mesh/D056728
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