von Willebrand Disease, Type 2

"von Willebrand Disease, Type 2" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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.

Descriptor ID	D056728
MeSH Number(s)	C15.378.100.100.900.200 C15.378.100.141.900.200 C15.378.463.920.200 C16.320.099.920.200
Concept/Terms	von Willebrand Disease, Type 2 von Willebrand Disease, Type 2 Type 2 von Willebrand Disease von Willebrand Disease, Type II Type II von Willebrand Disease von Willebrand Disease, Type 2N von Willebrand Disease, Type 2N Type IIN von Willebrand Disease von Willebrand Disease, Type IIN Type 2N von Willebrand Disease von Willebrand Disease, Type 2M von Willebrand Disease, Type 2M Type IIM von Willebrand Disease von Willebrand Disease, Type IIM Type 2M von Willebrand Disease von Willebrand Disease, Type 2A von Willebrand Disease, Type 2A Type IIA von Willebrand Disease von Willebrand Disease, Type IIA Type 2A von Willebrand Disease von Willebrand Disease, Type 2B von Willebrand Disease, Type 2B Type IIB von Willebrand Disease von Willebrand Disease, Type IIB Type 2B von Willebrand Disease

Below are MeSH descriptors whose meaning is more general than "von Willebrand Disease, Type 2".

Diseases [C]
Hemic and Lymphatic Diseases [C15]
Hematologic Diseases [C15.378]
Blood Coagulation Disorders [C15.378.100]
Blood Coagulation Disorders, Inherited [C15.378.100.100]
von Willebrand Diseases [C15.378.100.100.900]
von Willebrand Disease, Type 2 [C15.378.100.100.900.200]
Coagulation Protein Disorders [C15.378.100.141]
von Willebrand Diseases [C15.378.100.141.900]
von Willebrand Disease, Type 2 [C15.378.100.141.900.200]
Hemorrhagic Disorders [C15.378.463]
von Willebrand Diseases [C15.378.463.920]
von Willebrand Disease, Type 2 [C15.378.463.920.200]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Blood Coagulation Disorders, Inherited [C16.320.099]
von Willebrand Diseases [C16.320.099.920]
von Willebrand Disease, Type 2 [C16.320.099.920.200]

Below are MeSH descriptors whose meaning is related to "von Willebrand Disease, Type 2".

Below are MeSH descriptors whose meaning is more specific than "von Willebrand Disease, Type 2".

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