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Von Willebrand Disease — Gene Therapy & Clinical Trials | FollowGene
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Von Willebrand Disease
Von Willebrand Disease
Prevalence:
1/100
hematologic
Official
·
OMIM:193400
Official
·
ORPHA903
Most common hereditary bleeding disorder due to VWF gene mutations.
Associated Genes
VWF
Von Willebrand Factor
Chromosome 12
Autosomal Dominant