Definition

A von Willebrand's disease characterized by autosomal recessive inheritance of a severe quantitative defect or virtual absence of VWF in plasma, prolonged bleeding time, and more severe bleeding tendencies compared to the other types of von Willebrand disease that has_material_basis_in homozygous or compound heterozygous mutation in the VWF gene which maps to chromosome 12p13.

Synonyms

von Willebrand disease type 3
von Willebrand disease type III

Cross References

Parent Terms

von Willebrand's disease

Child Terms

None

Sources of Associations

Associated Genes

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Associated Alleles

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Associated Models

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von Willebrand's disease 3

von Willebrand's disease 3

Associated Genes

Associated Alleles

Associated Models