Search Ontology:
Human Disease

von Willebrand's disease 3

Term ID
DOID:0111054
Synonyms
  • 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)
References
  • ICD10CM:D68.03
  • MESH:D056729
  • MIM:277480
  • NCI:C85213
  • ORDO:166096
  • SNOMEDCT_US_2023_03_01:128108002
  • UMLS_CUI:C1264041
Ontology
Human Disease   ( DOID:0111054 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models