Von Willebrand Diseases
Disease ID: disease_node_7916
Connections displayed (default: 10).
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| Dbxref | GARD:7867, ICD10CM:D68.0, ICD9CM:286.4, MESH:D014842, NCI:C68677, SNOMEDCT_US_2023_03_01:11093006, UMLS_CUI:C0042974 |
|---|---|
| Subclassof | DOID_0061030 |
| Data Source | DOID, MESH |
| Synonyms | vascular hemophilia, vascular pseudohemophilia, von Willebrand disease, von Willebrand disorder, von Willebrand's-Jurgens' disease, von Willebrand-Jrgens disease |
| Mesh Id | D014842 |
| Mesh Label | von Willebrand Diseases |
| Mesh Subclassof | D020147, D001791, D025861, D006474 |
| Doid Label | von Willebrand's disease |
| Doid Description | A hemophilia that is a hereditary abnormality which slows the blood clotting process. It arises from a qualitative or quantitative deficiency of von Willebrand factor (vWF), a multimeric protein that is required for platelet adhesion. OMIM mapping confirmed by DO. [SN]. |
| Disease Node Id | disease_node_7916 |
| Doid Id | DOID_12531 |
| Label | Von Willebrand Diseases |
- Incoming r'ship
SUBCLASS_OFto/from Von Willebrand Disease, Type 3(ID:disease_node_12253) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Hemophilia(ID:disease_node_15603) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Von Willebrand Disease, Type 1(ID:disease_node_12245) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Von Willebrand Disease, Type 2(ID:disease_node_12249) (Disease)