D68.2
BillableHereditary deficiency of other clotting factors
D68.2 is the ICD-10-CM code for Hereditary deficiency of other clotting factors. It is a billable, specific code valid for reimbursement.
D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
Includes
- •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
Frequently asked questions
- What is ICD-10 code D68.2?
- D68.2 is the ICD-10-CM code for "Hereditary deficiency of other clotting factors". It falls under D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism.
- Is D68.2 a billable code?
- Yes — D68.2 is a billable, specific ICD-10-CM code valid for reimbursement.
Source: CMS ICD-10-CM FY2026. For informational purposes only — not medical advice. See our medical disclaimer.
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