List of diseases covered by
Coagulation Disorders NGS panel
| Gene | Condition |
| F2 | Hypoprothrombinemia; Thrombophilia due to thrombin defect |
| F5 | Factor V deficiency; Thrombophilia due to activated protein C resistance |
| F8 | Hemophilia A |
| F9 | Hemophilia B; Thrombophilia, X-linked, due to factor IX defect |
| F10 | Factor X deficiency |
| F11 | Factor XI deficiency |
| F12 | Factor XII deficiency; Angioedema, hereditary, type III |
| F13A1 | Factor XIIIA deficiency |
| FGA | Afibrinogenemia, congenital; Amyloidosis, familial visceral; Dysfibrinogenemia, congenital |
| FGB | Afibrinogenemia, congenital; Dysfibrinogenemia, congenital |
| FGG | Afibrinogenemia, congenital; Dysfibrinogenemia, congenital |
| GGCX | Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency; Vitamin K-dependent clotting factors, combined deficiency of, 1 |
| LMAN1 | Combined factor V and VIII deficiency |
| MCFD2 | Factor V and factor VIII, combined deficiency of |
| SERPINC1 | Thrombophilia due to antithrombin III deficiency |
| VKORC1 | Vitamin K-dependent clotting factors, combined deficiency of, 2; Warfarin resistance |
| VWF | von Willebrand disease, type 1; von Willebrand disease, types 2A, 2B, 2M, and 2N; von Willibrand disease, type 3 |