Structured Summary
Abstract
Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion.
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Classification
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See Also
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Synonyms
16 entry terms
- Angiohemophilia
- Hemophilia, Vascular
- Vascular Pseudohemophilia
- Von Willebrand Disorder
- Von Willebrand's Factor Deficiency
- von Willebrand Disease
- von Willebrand's Disease
- von Willebrand's Diseases
- Angiohemophilias
- Disorder, Von Willebrand
- Pseudohemophilia, Vascular
- Pseudohemophilias, Vascular
- Vascular Hemophilia
- Vascular Hemophilias
- Vascular Pseudohemophilias
- von Willebrand Disease, Recessive Form
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
Indexing Annotation
note specific types of Von Willebrand Disease are available
MeSH Record
History Note
2010(1963)
MeSH Hierarchy
Tree Numbers
MeSH Record
NLM Classification
WH 312
AMA Style
References
- National Library of Medicine. von Willebrand Diseases. Medical Subject Headings (MeSH). 2026. Unique ID D014842. http://id.nlm.nih.gov/mesh/2026/D014842
- von Willebrand Diseases. In: Wikipedia. https://en.wikipedia.org/wiki/Von_Willebrand_disease
- von Willebrand Diseases. In: Wikidata. https://www.wikidata.org/wiki/Q709360