MeSH Browser

MeSH Supplementary: Von Willebrand disease, platelet type
Unique ID: C536458
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536458
Entry Term(s): Platelet-type Von Willebrand disease; Pseudo-Von Willebrand disease; Von Willebrand Disease, Platelet-Type
Registry Number: 0
Heading Mapped to: *von Willebrand Diseases
Frequency: 29
Note: An autosomal dominant bleeding disorder characterized by abnormally enhanced binding of VON WILLEBRAND FACTOR by the PLATELET GLYCOPROTEIN GPIB-IX COMPLEX. Mutations in the GP1BA gene have been identified. OMIM: 177820
Date of Entry: 2010/08/25
Revision Date: 2015/08/18

Von Willebrand disease, platelet type MeSH Supplementary Concept Data 2024