|OBO ID: DOID:0111054|
|Term Name:||von Willebrand's disease 3||Search Ontology:|
|Definition:||A von Willebrand's disease characterized by autosomal recessive inheritance of a severe quantitative defect or virtual absence of VWF in plasma, prolonged bleeding time, and more severe bleeding tendencies compared to the other types of von Willebrand disease that has material_basis_in homozygous or compound heterozygous mutation in the VWF gene which maps to chromosome 12p13. (2)|
|Ontology:||Human Disease (DOID:0111054)|
|is a type of:||
OTHER von Willebrand's disease 3 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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