D68.2
Hereditary deficiency of other clotting factors
Billable
Code Hierarchy
D68D68.2
Coding Guidelines
Inclusion Terms
- AC globulin deficiency
- Congenital afibrinogenemia
- Deficiency of factor I [fibrinogen]
- Deficiency of factor II [prothrombin]
- Deficiency of factor V [labile]
- Deficiency of factor VII [stable]
- Deficiency of factor X [Stuart-Prower]
- Deficiency of factor XII [Hageman]
- Deficiency of factor XIII [fibrin stabilizing]
- Dysfibrinogenemia (congenital)
- Hypoproconvertinemia
- Owren's disease
- Proaccelerin deficiency
Related Codes
D68.0Category
Von Willebrand disease
D68.1Billable
Hereditary factor XI deficiency
D68.3Category
Hemorrhagic disorder due to circulating anticoagulants
D68.4Billable
Acquired coagulation factor deficiency
D68.5Category
Primary thrombophilia
D68.6Category
Other thrombophilia
D68.8Billable
Other specified coagulation defects
D68.9Billable
Coagulation defect, unspecified
