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Von Willebrand disease type 2M
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Disease definition
A subtype of type 2 von Willebrand disease characterized by a bleeding disorder associated with decreased affinity of the Willebrand factor (VWF) for platelets or collagen in the absence of any deficiency of high molecular weight VWF multimers. The disease manifests as mucocutaneous bleeding (menorrhagia, epistaxis, gastrointestinal hemorrhage, etc.).
ORPHA:166090
Detailed information
: produced/endorsed by ERN(s)
: produced/endorsed by FSMR(s)
General public
Article for general public
Guidelines
Emergency guidelines
Anesthesia guidelines
Clinical practice guidelines
Disease review articles
Clinical genetics review
Patient-Centered Outcome Measures (PCOMs)
Access questionnaires assessing quality of life in this disease
(English)
Additional information
Further information on this disease
Patient-centred resources for this disease
Research activities on this disease
- Research project(s) (40)
- Clinical trial(s) (8)
- Biobank(s) (10)
- Registry(ies) (36)
- Network of experts (7)
Newborn screening
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