An instance of thrombophilia that is inherited.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Hereditary thrombophilia due to congenital protein C deficiency | MONDO:0019145 | 2 | |
| Hereditary thrombophilia due to congenital protein S deficiency | MONDO:0019144 | 2 | |
| Factor 5 excess with spontaneous thrombosis | MONDO:0007594 | ||
| Heparin cofactor 2 deficiency | MONDO:0012876 | SERPIND1 | |
| Hereditary antithrombin deficiency | MONDO:0013144 | SERPINC1 | |
| Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency | MONDO:0013143 | HRG | |
| Thrombomodulin-related bleeding disorder | MONDO:0013775 | THBD | |
| Thrombophilia due to activated protein C resistance | MONDO:0008560 | F5 | |
| Thrombophilia due to thrombin defect | MONDO:0008559 | ||
| Thrombophilia, X-linked, due to factor 8 defect | MONDO:0859082 | F8 | |
| Thrombophilia, X-linked, due to factor 9 defect | MONDO:0010432 | F9 | |
| Thrombophilia, familial, due to decreased release of tissue plasminogen activator | MONDO:0012872 |
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