FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term von Willebrand's disease 3 ID (Ontology) DOID:0111054 (Human Disease)
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.
Also Known As "von Willebrand disease type 3" ; "von Willebrand disease type III" ; "VWD type 3" (for all, see Synonyms field below)
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 Genes
 von Willebrand's disease 3       1
 for disease ribbon | von Willebrand's disease 3       1
 model of | von Willebrand's disease 3       1
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  hemophilia
   |__von Willebrand's disease
       |__von Willebrand's disease 3  1 rec.
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Synonyms
  • "von Willebrand disease type 3" EXACT
    "von Willebrand disease type III" EXACT
    "VWD type 3" EXACT
    "VWD3" EXACT OMO:0003012
Secondary IDs
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ICD10CM:D68.03
MESH:D056729
MIM:277480
NCI:C85213
ORDO:166096
SNOMEDCT_US_2023_03_01:128108002
UMLS_CUI:C1264041