Prothrombin Thrombophilia
Disease ID: disease_node_17043
Connections displayed (default: 10).
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| Dbxref | MIM:188050 |
|---|---|
| Subclassof | DOID_2452, DOID_0050736 |
| Data Source | DOID |
| Doid Label | prothrombin thrombophilia |
| Doid Description | A thrombophilia that is characterized by increases the risk of blood clots including deep vein thrombosis and pulmonary embolism and that has_material_basis_in heterozygous mutation in the thrombin gene (F2 gene) on chromosome 11p11. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_17043 |
| Doid Id | DOID_0080701 |
| Label | Prothrombin Thrombophilia |
- Outgoing r'ship
SUBCLASS_OFto/from Thrombophilia(ID:disease_node_10025) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)