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.
Inclusion Term
- 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:
Section: D65-D69 Coagulation defects, purpura and other hemorrhagic conditions
Category: D68 Other coagulation defects
Billable/Specific Code
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Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
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