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 2 ID (Ontology) DOID:0060574 (Human Disease)
Definition A von Willebrand's disease characterized by qualitative but not quantitative abnormalities of the VWF protein that has_material_basis_in mutation in the VWF gene which maps to chromosome 12p13.
Also Known As "von Willebrand disease type 2" ; "von Willebrand disease type II" ; "VWD type 2" (for all, see Synonyms field below)
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 Genes
 von Willebrand's disease 2       1
 for disease ribbon | von Willebrand's disease 2       1
 model of | von Willebrand's disease 2       1
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  hemophilia
   |__von Willebrand's disease
       |__von Willebrand's disease 2  1 rec.
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Synonyms
  • "von Willebrand disease type 2" EXACT
    "von Willebrand disease type II" EXACT
    "VWD type 2" EXACT
    "VWD2" EXACT OMO:0003012
Secondary IDs
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ICD10CM:D68.02
MESH:D056728
MIM:613554
ORDO:166081
SNOMEDCT_US_2023_03_01:128107007
UMLS_CUI:C1264040