Term Name: | von Willebrand's disease 2 |
---|---|
Synonyms: | von Willebrand disease type 2, von Willebrand disease type II, VWD type 2, VWD2 |
Definition: | A 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. |
Ontology: | Human Disease [DOID:0060574] ( DOID:0060574 ) |