Platelet-Type Bleeding Disorder 3
Disease ID: disease_node_17056
Connections displayed (default: 10).
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| Dbxref | ICD10CM:D69.8, MIM:177820, ORDO:52530 |
|---|---|
| Subclassof | DOID_0050736, DOID_2218 |
| Data Source | DOID |
| Synonyms | BDPLT3, PT-VWD, platelet type-von Willebrand disease, pseudo-von Willebrand disease, von Willebrand disease platelet-type |
| Doid Label | platelet-type bleeding disorder 3 |
| Doid Description | A blood platelet disease characterized by enhanced binding of von Willebrand factor by the platelet glycoprotein Ib receptor complex that has_material_basis_in mutation in the GP1BA gene on chromosome 17p13.2. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_17056 |
| Doid Id | DOID_0111056 |
| Label | Platelet-Type Bleeding Disorder 3 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Blood Platelet Disorders(ID:disease_node_1622) (Disease)