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. [ url:https://www.ncbi.nlm.nih.gov/pubmed/20409624 http://purl.obolibrary.org/obo/ECO_0007645 ]
Synonyms: von Willebrand disease type II VWD2 von Willebrand disease type 2 VWD type 2
Term information
- MIM:613554
- SNOMEDCT_US_2023_03_01:128107007
- UMLS_CUI:C1264040
- ORDO:166081
- ICD10CM:D68.02
- MESH:D056728
DO_rare_slim