Von Willebrand Disease, Type 1
Disease ID: disease_node_12245
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| Dbxref | ICD10CM:D68.01, MESH:D056725, MIM:193400, NCI:C131685, SNOMEDCT_US_2023_03_01:128106003, UMLS_CUI:C1264039 |
|---|---|
| Subclassof | DOID_12531 |
| Data Source | DOID, MESH |
| Synonyms | VWD type 1, VWD1, von Willebrand disease type 1, von Willebrand disease type I |
| Mesh Id | D056725 |
| Mesh Label | von Willebrand Disease, Type 1 |
| Mesh Subclassof | D014842 |
| Doid Label | von Willebrand's disease 1 |
| Doid Description | A von Willebrand's disease characterized by quantitative partial deficiency of circulating VWF that has_material_basis_in heterozygous mutation in the VWF gene on chromosome 12p13. |
| Disease Node Id | disease_node_12245 |
| Doid Id | DOID_0060573 |
| Label | Von Willebrand Disease, Type 1 |
- Outgoing r'ship
SUBCLASS_OFto/from Von Willebrand Diseases(ID:disease_node_7916) (Disease)