D68.2: Hereditary deficiency of other clotting factors
D68.2 is a billable, specific ICD-10-CM code for hereditary deficiency of other clotting factors. It is valid for submission on a claim.
Check D68.2 with the rest of the claim: free scrubberInclusion terms
Alternative wordings a physician may use in the chart for this same code.
- 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
Excludes1 inherited from the categories above D68.2
A category’s note binds every code beneath it.
Excludes2 inherited from the categories above D68.2
Not part of this code, but both may be coded when both are present.
Other codes that can never be billed with D68.2
Their own Excludes1 notes name this code, so the conflict is not listed above.
- R79.1Abnormal coagulation profile
Risk adjustment
D68.2 risk-adjusts. Under the CMS-HCC V28 model it maps to this category:
- HCC 112 Immune Thrombocytopenia and Specified Coagulation Defects and Hemorrhagic Conditions0.450 RAF
Coefficient shown for the Community Non-dual Aged segment. A higher HCC in the same hierarchy will suppress this one, so capturing it does not always add score. Look up the whole chart to see which of its HCCs the hierarchy would zero.
Medicare coverage
D68.2 is named in 3 Medicare coverage policies: 3 listing it as supporting medical necessity. Which one applies depends on your Medicare contractor.
- A56065Billing and Coding: Guidance for Anti-Inhibitor Coagulant Complex (AICC) National Coverage Determination (NCD) 110.3
- A56416Billing and Coding: Assays for Vitamins and Metabolic Function
- A57954Billing and Coding: Routine Foot Care
Alphabetic index entries that lead here
- Dysfibrinogenemia(congenital)
- Fibrinopenia(hereditary)
- Hageman's factor defect, deficiency or disease
- Hypoproconvertinemia, congenital(hereditary)
- Hypoprothrombinemia(congenital) (hereditary) (idiopathic)
- Owren's disease or syndrome(parahemophilia)
- Parahemophilia
- Stuart deficiency disease(factor X)
- Stuart-Prower factor deficiency(factor X)
- Absence›fibrinogen(congenital)
- Afibrinogenemia›congenital
- Defect, defective›fibrin polymerization
Code history
Unchanged in every release from FY2024 to FY2027.