1. Home
2. ICD-10 Codes
3. Chapter - D50-D89
4. Section - D65-D69
5. Category - D68
6. D68.2

D68.2 - Hereditary deficiency of other clotting factors

• Applicable to Hereditary deficiency of other clotting factors
• The 2025 edition of ICD10-CM D68.2 became effective on October 1, 2024.
• This is the American ICD10-CM version of D68.2 - other international versions of ICD10 D68.2 may differ.
• D68.2 is a Billable / Specific ICD10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

• 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

The following codes above D68.2 contain annotation back-references that may be applicable to D68.2:

• Chapter: D50-D89 - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
• Section: D65-D69 - Coagulation defects, purpura and other hemorrhagic conditions
• Category: D68 - Other coagulation defects

Browse other similar CM codes:

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.