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.
Inclusion 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
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.
Medicare coverage
D68.2 is named in 4 Medicare coverage policies — 4 listing it as supporting medical necessity. Which of them applies to you depends on your Medicare contractor, and coverage genuinely differs by state.
- A56065Billing and Coding: Guidance for Anti-Inhibitor Coagulant Complex (AICC) National Coverage Determination (NCD) 110.3
- 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
How D68.2 is indexed
Coders do not find codes by browsing the tabular list — they look them up in the alphabetic index, under the word the physician wrote. These are the index entries that lead here, so you can see which chart wordings map to D68.2.
- 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
Related codes at this level
Codes that share D68. If D68.2 is not quite right, the correct code is usually one of these.
Questions about D68.2
- Is D68.2 a billable ICD-10-CM code?
- Yes. D68.2 is a billable, specific ICD-10-CM code and is valid for submission on a claim.
- Where does D68.2 sit in the tabular list?
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89), in the block Coagulation defects, purpura and other hemorrhagic conditions (D65-D69).