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Hemic and Lymphatic Diseases > Hematologic Diseases > Hemorrhagic Disorders > von Willebrand Diseases > von Willebrand Disease, Type 1
... > Hemic and Lymphatic Diseases > Hematologic Diseases > Blood Coagulation Disorders > Coagulation Protein Disorders > von Willebrand Diseases > von Willebrand Disease, Type 1
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Blood Coagulation Disorders, Inherited > von Willebrand Diseases > von Willebrand Disease, Type 1
... > Hemic and Lymphatic Diseases > Hematologic Diseases > Blood Coagulation Disorders > Blood Coagulation Disorders, Inherited > von Willebrand Diseases > von Willebrand Disease, Type 1
Hemic and Lymphatic Diseases > Hematologic Diseases > Blood Platelet Disorders > von Willebrand Diseases > von Willebrand Disease, Type 1

Preferred term

von Willebrand Disease, Type 1  

Type

  • Topical Descriptor

Broader concept

Related concepts

Entry terms

  • Type 1 von Willebrand Disease
  • Type I von Willebrand Disease
  • von Willebrand Disease, Type I

Scope note

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

History note

  • 2010

In other languages

URI

http://www.yso.fi/onto/mesh/D056725

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