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Hemic and Lymphatic Diseases > Hematologic Diseases > Blood Platelet Disorders > von Willebrand Diseases > von Willebrand Disease, Type 3
Hemic and Lymphatic Diseases > Hematologic Diseases > Hemorrhagic Disorders > von Willebrand Diseases > von Willebrand Disease, Type 3
... > Hemic and Lymphatic Diseases > Hematologic Diseases > Blood Coagulation Disorders > Blood Coagulation Disorders, Inherited > von Willebrand Diseases > von Willebrand Disease, Type 3
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Blood Coagulation Disorders, Inherited > von Willebrand Diseases > von Willebrand Disease, Type 3
... > Hemic and Lymphatic Diseases > Hematologic Diseases > Blood Coagulation Disorders > Coagulation Protein Disorders > von Willebrand Diseases > von Willebrand Disease, Type 3

Preferred term

von Willebrand Disease, Type 3  

Type

  • Topical Descriptor

Broader concept

Related concepts

Entry terms

  • Type 3 Von Willebrand's Disease
  • Type 3 VWD
  • Von Willebrand Disease, Severe Form

Scope note

  • A subtype of von Willebrand disease that results from a total or near total deficiency of VON WILLEBRAND FACTOR.

History note

  • 2010

In other languages

URI

http://www.yso.fi/onto/mesh/D056729

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