|OBO ID: DOID:0060573|
|Term Name:||von Willebrand's disease 1||Search Ontology:|
|Definition:||A von Willebrand's disease characterized by quantitative partial deficiency of circulating VWF that has material_basis_in heterozygous mutation in the VWF gene on chromosome 12p13. (2)|
|Ontology:||Human Disease (DOID:0060573)|
|is a type of:||
OTHER von Willebrand's disease 1 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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