| Metadata | |
|---|---|
| ID | DOID:0060574 |
| Name | von Willebrand's disease 2 |
| 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. https://www.ncbi.nlm.nih.gov/pubmed/20409624 |
| Xrefs |
SNOMEDCT_US_2023_03_01:128107007 |
| Subsets |
DO_rare_slim |
| Synonyms |
von Willebrand disease type 2 [EXACT] von Willebrand disease type II [EXACT] VWD type 2 [EXACT] VWD2 [EXACT] |
| Parent Relationships |