Type 2 von Willebrand Disease

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.

Also Known As:

von Willebrand Disease, Type 2; Type 2A von Willebrand Disease; Type 2B von Willebrand Disease; Type 2M von Willebrand Disease; Type 2N von Willebrand Disease; Type II von Willebrand Disease; Type IIA von Willebrand Disease; Type IIB von Willebrand Disease; Type IIM von Willebrand Disease; Type IIN von Willebrand Disease; von Willebrand Disease, Type 2A; von Willebrand Disease, Type 2B; von Willebrand Disease, Type 2M; von Willebrand Disease, Type 2N; von Willebrand Disease, Type II; von Willebrand Disease, Type IIA; von Willebrand Disease, Type IIB; von Willebrand Disease, Type IIM; von Willebrand Disease, Type IIN

Hemic and Lymphatic Diseases: 6
- Hematologic Diseases: 3366
  - Hemorrhagic Disorders: 702
    - von Willebrand Diseases: 2295
      - Type 2 von Willebrand Disease: 260
  - Blood Coagulation Disorders: 167
    - Inherited Blood Coagulation Disorders: 74
      - von Willebrand Diseases: 2295
        Type 2 von Willebrand Disease: 260
    - Coagulation Protein Disorders: 1
      - von Willebrand Diseases: 2295
        Type 2 von Willebrand Disease: 260
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Inherited Blood Coagulation Disorders: 74
    - von Willebrand Diseases: 2295
      - Type 2 von Willebrand Disease: 260

D Rapson Selected Research

D Rapson Research Topics

Disease

Drug/Important Bio-Agent (IBA)