FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term von Willebrand's disease ID (Ontology) DOID:12531 (Human Disease)
Definition A hemophilia that is a hereditary abnormality which slows the blood clotting process. It arises from a qualitative or quantitative deficiency of von Willebrand factor (vWF), a multimeric protein that is required for platelet adhesion.
Also Known As "vascular hemophilia" ; "vascular pseudohemophilia" ; "von Willebrand disease" (for all, see Synonyms field below)
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
No relevant statements available
Spanning Tree (Parents/Children)
Only view relationship:
  blood coagulation disease
   |__hemophilia
       |__von Willebrand's disease  1 rec.
           |__von Willebrand's disease 1 1 rec.
           |__von Willebrand's disease 2 1 rec.
           |__von Willebrand's disease 3 1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a hemophilia
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "vascular hemophilia" EXACT
    "vascular pseudohemophilia" EXACT
    "von Willebrand disease" EXACT
    "von Willebrand disorder" EXACT
    "von Willebrand's-Jurgens' disease" EXACT
    "von Willebrand-Jrgens disease" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
GARD:7867
ICD10CM:D68.0
ICD9CM:286.4
MESH:D014842
NCI:C68677
SNOMEDCT_US_2023_03_01:11093006
UMLS_CUI:C0042974