OBO ID: DOID:0111054
Term Name: von Willebrand's disease 3 Search Ontology:
  • von Willebrand disease type 3
  • von Willebrand disease type III
  • VWD type 3
  • VWD3
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)
OTHER von Willebrand's disease 3 PAGES
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
VWF von Willebrand disease, type 3 277480
ZEBRAFISH MODELS No data available
PHENOTYPE No data available