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Hemic and Lymphatic Diseases > Hematologic Diseases > Hemorrhagic Disorders > von Willebrand Diseases > von Willebrand Disease, Type 2
... > Hemic and Lymphatic Diseases > Hematologic Diseases > Blood Coagulation Disorders > Coagulation Protein Disorders > von Willebrand Diseases > von Willebrand Disease, Type 2
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Blood Coagulation Disorders, Inherited > von Willebrand Diseases > von Willebrand Disease, Type 2
... > Hemic and Lymphatic Diseases > Hematologic Diseases > Blood Coagulation Disorders > Blood Coagulation Disorders, Inherited > von Willebrand Diseases > von Willebrand Disease, Type 2
Hemic and Lymphatic Diseases > Hematologic Diseases > Blood Platelet Disorders > von Willebrand Diseases > von Willebrand Disease, Type 2

Preferred term

von Willebrand Disease, Type 2  

Type

  • Topical Descriptor

Broader concept

Related concepts

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

URI

http://www.yso.fi/onto/mesh/D056728

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