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von Willebrand disease type 2

disorder
SNOMED 128107007CUI C1264040

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Research Evidence

Peer-reviewed studies linked via MeSH term "von Willebrand Disease, Type 2" from the MEDLINE/PubMed database.

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Laboratory assays of VWF activity and use of desmopressin trials in the diagnosis of VWD: a systematic review and meta-analysis.
[object Object], [object Object], [object Object] et al. · Blood Adv · 2022
PMID: 35192687Meta-AnalysisFull text (PMC)
Type 2B von Willebrand Disease in Pregnancy: A Systematic Literature Review.
[object Object], [object Object], [object Object] et al. · Semin Thromb Hemost · 2021
PMID: 33636751Meta-Analysis
A randomised pilot trial of the anti-von Willebrand factor aptamer ARC1779 in patients with type 2b von Willebrand disease.
[object Object], [object Object], [object Object] et al. · Thromb Haemost · 2010
PMID: 20589313RCT
Von Willebrand Factor Multimer Analysis and Classification: A Comprehensive Review and Updates.
[object Object], [object Object], [object Object] et al. · Semin Thromb Hemost · 2023
PMID: 36174612Review
Von Willebrand disease type 2N: An update.
[object Object], [object Object], [object Object] · J Thromb Haemost · 2021
PMID: 33497541Review
How I manage severe von Willebrand disease.
[object Object], [object Object] · Br J Haematol · 2019
PMID: 31498884ReviewFull text (PMC)
How I treat type 2B von Willebrand disease.
[object Object], [object Object] · Blood · 2018
PMID: 29378695Review
Diagnostic Differentiation of von Willebrand Disease Types 1 and 2 by von Willebrand Factor Multimer Analysis and DDAVP Challenge Test.
[object Object], [object Object], [object Object] et al. · Clin Appl Thromb Hemost · 2017
PMID: 27443694Review
Advances in the diagnosis and treatment of Von Willebrand disease.
[object Object], [object Object] · Hematology Am Soc Hematol Educ Program · 2017
PMID: 29222282ReviewFull text (PMC)
Diagnosing von Willebrand disease: genetic analysis.
[object Object] · Hematology Am Soc Hematol Educ Program · 2016
PMID: 27913546ReviewFull text (PMC)

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Bruising susceptibility
HP:0000978
Frequent nosebleeds
HP:0000421
Hypermenorrhea
HP:0000132
Low platelet count
HP:0001873

Quick Facts

SNOMED CT
128107007
UMLS CUI
C1264040
Fully Specified Name
Hereditary von Willebrand disease type 2 (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
4
Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.