von Willebrand Disease, Type 3

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

Year introduced: 2010

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Tree Number(s): C15.378.100.100.900.300, C15.378.100.141.900.300, C15.378.463.920.300, C16.320.099.920.300

MeSH Unique ID: D056729

Entry Terms:

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

Previous Indexing:

• von Willebrand Disease (1968-2009)

All MeSH Categories
Diseases Category
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Blood Coagulation Disorders, Inherited
von Willebrand Diseases
von Willebrand Disease, Type 3

All MeSH Categories
Diseases Category
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Coagulation Protein Disorders
von Willebrand Diseases
von Willebrand Disease, Type 3

All MeSH Categories
Diseases Category
Hemic and Lymphatic Diseases
Hematologic Diseases
Hemorrhagic Disorders
von Willebrand Diseases
von Willebrand Disease, Type 3

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
von Willebrand Diseases
von Willebrand Disease, Type 3