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von Willebrand's disease 1

MeSH: D056725ORPHA: 166078

Contents

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

Overview

von Willebrand's disease characterized by quantitative partial deficiency of circulating VWF that has material basis in heterozygous mutation in the VWF gene on chromosome 12p13

Available Treatments (0)

No treatments linked yet

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

Classification & Codes

MeSH Code

D056725

Orphanet Code

ORPHA:166078
von Willebrand's disease 1
MeSHD056725
OrphanetORPHA:166078
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO
von Willebrand's disease 1 | OrphanDrug