Von Willebrand Disease, Type 2
Disease ID: disease_node_12249
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| Dbxref | ICD10CM:D68.02, MESH:D056728, MIM:613554, ORDO:166081, SNOMEDCT_US_2023_03_01:128107007, UMLS_CUI:C1264040 |
|---|---|
| Subclassof | DOID_12531 |
| Data Source | DOID, MESH |
| Synonyms | VWD type 2, VWD2, von Willebrand disease type 2, von Willebrand disease type II |
| Mesh Id | D056728 |
| Mesh Label | von Willebrand Disease, Type 2 |
| Mesh Subclassof | D014842 |
| Doid Label | von Willebrand's disease 2 |
| Doid Description | 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. |
| Disease Node Id | disease_node_12249 |
| Doid Id | DOID_0060574 |
| Label | Von Willebrand Disease, Type 2 |
- Outgoing r'ship
SUBCLASS_OFto/from Von Willebrand Diseases(ID:disease_node_7916) (Disease)