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von Willebrand's disease 2

MeSH: D056728ORPHA: 166081

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Classification & Codes

Overview

von Willebrand's disease characterized by qualitative but not quantitative abnormalities of the VWF protein that has material basis in mutation in the VWF gene which maps to chromosome 12p13

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Classification & Codes

MeSH Code

D056728

Orphanet Code

ORPHA:166081
von Willebrand's disease 2
MeSHD056728
OrphanetORPHA:166081
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO
von Willebrand's disease 2 | OrphanDrug