von Willebrand's disease 2

Summary
Synonym
  • VWD type 2
  • VWD2
  • von Willebrand disease type 2
  • von Willebrand disease type II
Definition
A von Willebrand's disease characterized by qualitative but not quantitative abnormalities of the VWF protein that has_material_basis_in mutation in the VWF gene which maps to chromosome 12p13.
Super Class
von Willebrand's disease
Disease Ontology
DOID:0060574
Mondo Disease Ontology
MeSH
UMLS
ORDO
MGI genotype (from TogoID)
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
3673 ITGA2 integrin subunit alpha 2
7450 VWF von Willebrand factor
Displaying 1 entry
Gene ID Gene Symbol Description Source
22371 Vwf Von Willebrand factor
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
Q8CIZ8 von Willebrand factor

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 7, 2025