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 1 ID (Ontology) DOID:0060573 (Human Disease)
Definition A von Willebrand's disease characterized by quantitative partial deficiency of circulating VWF that has_material_basis_in heterozygous mutation in the VWF gene on chromosome 12p13.
Also Known As "von Willebrand disease type 1" ; "von Willebrand disease type I" ; "VWD type 1" (for all, see Synonyms field below)
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 Genes
 von Willebrand's disease 1       1
 for disease ribbon | von Willebrand's disease 1       1
 model of | von Willebrand's disease 1       1
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  hemophilia
   |__von Willebrand's disease
       |__von Willebrand's disease 1  1 rec.
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Is a von Willebrand's disease
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Synonyms
  • "von Willebrand disease type 1" EXACT
    "von Willebrand disease type I" EXACT
    "VWD type 1" EXACT
    "VWD1" EXACT OMO:0003012
Secondary IDs
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ICD10CM:D68.01
MESH:D056725
MIM:193400
NCI:C131685
SNOMEDCT_US_2023_03_01:128106003
UMLS_CUI:C1264039