Von Willebrand Disease, Type 3
Disease ID: disease_node_12253
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| Dbxref | ICD10CM:D68.03, MESH:D056729, MIM:277480, NCI:C85213, ORDO:166096, SNOMEDCT_US_2023_03_01:128108002, UMLS_CUI:C1264041 |
|---|---|
| Subclassof | DOID_12531 |
| Data Source | DOID, MESH |
| Synonyms | VWD type 3, VWD3, von Willebrand disease type 3, von Willebrand disease type III |
| Mesh Id | D056729 |
| Mesh Label | von Willebrand Disease, Type 3 |
| Mesh Subclassof | D014842 |
| Doid Label | von Willebrand's disease 3 |
| Doid Description | A von Willebrand's disease characterized by autosomal recessive inheritance of a severe quantitative defect or virtual absence of VWF in plasma, prolonged bleeding time, and more severe bleeding tendencies compared to the other types of von Willebrand disease that has_material_basis_in homozygous or compound heterozygous mutation in the VWF gene which maps to chromosome 12p13. |
| Has Symptom | SYMP_0000007 |
| Disease Node Id | disease_node_12253 |
| Doid Id | DOID_0111054 |
| Label | Von Willebrand Disease, Type 3 |
- Outgoing r'ship
HAS_SYMPTOMto/from Bleeding(ID:disease_node_21108) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Von Willebrand Diseases(ID:disease_node_7916) (Disease)