Thrombophilia
Disease ID: disease_node_10025
Connections displayed (default: 10).
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| Dbxref | ICD10CM:D68.59, MESH:D019851, MIM:PS188050, NCI:C84479, SNOMEDCT_US_2023_03_01:191302007, UMLS_CUI:C0398623 |
|---|---|
| Subclassof | DOID_1247 |
| Data Source | DOID, MESH |
| Synonyms | hypercoagulability state |
| Mesh Id | D019851 |
| Mesh Label | Thrombophilia |
| Mesh Subclassof | D006402 |
| Doid Label | thrombophilia |
| Doid Description | A blood coagulation disease that is characterized by an increased tendency to form clots. OMIM mapping confirmed by DO. [LS]. |
| Disease Node Id | disease_node_10025 |
| Doid Id | DOID_2452 |
| Label | Thrombophilia |
- Incoming r'ship
SUBCLASS_OFto/from Thrombophilia Due To Hrg Deficiency(ID:disease_node_17042) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Thrombophilia Due To Thrombin Defect(ID:disease_node_17041) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Blood Coagulation Disorders(ID:disease_node_1621) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Purpura, Thrombotic Thrombocytopenic(ID:disease_node_6474) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Protein S Deficiency(ID:disease_node_9711) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Protein C Deficiency(ID:disease_node_10116) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Prothrombin Thrombophilia(ID:disease_node_17043) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Disseminated Intravascular Coagulation(ID:disease_node_2560) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Antithrombin Iii Deficiency(ID:disease_node_10120) (Disease)