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Hemic and Lymphatic Diseases > Hematologic Diseases > Hemorrhagic Disorders > von Willebrand Diseases > von Willebrand Disease, Type 2
... > Hemic and Lymphatic Diseases > Hematologic Diseases > Blood Coagulation Disorders > Coagulation Protein Disorders > von Willebrand Diseases > von Willebrand Disease, Type 2
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Blood Coagulation Disorders, Inherited > von Willebrand Diseases > von Willebrand Disease, Type 2
... > Hemic and Lymphatic Diseases > Hematologic Diseases > Blood Coagulation Disorders > Blood Coagulation Disorders, Inherited > von Willebrand Diseases > von Willebrand Disease, Type 2
Hemic and Lymphatic Diseases > Hematologic Diseases > Blood Platelet Disorders > von Willebrand Diseases > von Willebrand Disease, Type 2

Término preferido

von Willebrand Disease, Type 2  

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Tipo

  • mesh:Descriptor

Definición

  • 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.

Concepto genérico

Conceptos relacionados

Etiquetas alternativas

  • Type 2 von Willebrand Disease
  • Type II von Willebrand Disease
  • von Willebrand Disease, Type II

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-PWJMSVK4-V

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RDF/XML TURTLE JSON-LD Creado 6/7/09