Search Ontology:
Human Disease

von Willebrand's disease 2

Term ID
DOID:0060574
Synonyms
  • von Willebrand disease type 2
  • von Willebrand disease type II
  • VWD type 2
  • VWD2
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. https://www.ncbi.nlm.nih.gov/pubmed/20409624
References
Ontology
Human Disease   ( DOID:0060574 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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