|OBO ID: DOID:0060574|
|Term Name:||von Willebrand's disease 2||Search Ontology:|
|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|
|Ontology:||Human Disease (DOID:0060574)|
|is a type of:||
OTHER von Willebrand's disease 2 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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