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VWF

—Von Willebrand Factor

Chromosome: 12

Location: 12:5948877-6124770

OMIM: 613160

Ensembl: ENSG00000110799

Official·OMIM:613160 Official·ENSG00000110799

Encodes von Willebrand factor. Mutations cause von Willebrand disease.

Treatment Roadmap — VWF

Preclinical

Phase 1

Phase 2

2 trial

Phase 3

1 trial

Approved

Clinical trials have approximately 10% success rate. This roadmap shows the current status, not guaranteed outcomes.

Associated Diseases

Von Willebrand Disease

Autosomal DominantPrevalence: 1/100hematologic

Official·OMIM:193400 Official·ORPHA903

Summary

Clinical Trial

Approved Therapy

Registered Variant