D68.2
Billable codeHereditary deficiency of other clotting factors
The ICD-10 code for hereditary deficiency of other clotting factors is D68.2.
Clinical notes
Also known as
Alternate wording, synonyms, or specific conditions that fall under this code, listed to help confirm you've picked the right one.
- 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
Documentation support
General coding-documentation guidance — not a substitute for payer-specific requirements or professional coding judgment.
- •As a general rule, code to the highest level of specificity supported by the documentation in the medical record.
Related codes in this category
- D68.0Von Willebrand diseasenon-billable header
- D68.1Hereditary factor XI deficiency
- D68.3Hemorrhagic disorder due to circulating anticoagulantsnon-billable header
- D68.4Acquired coagulation factor deficiency
- D68.5Primary thrombophilianon-billable header
- D68.6Other thrombophilianon-billable header
- D68.8Other specified coagulation defects
- D68.9Coagulation defect, unspecified
- D68.2Hereditary deficiency of other clotting factors
ICD-9-CM equivalent
Informational only — GEM mappings are approximate, not guaranteed one-to-one equivalents. Verify before use in billing.
- 2863
Associated MS-DRGs
D68.2 can serve as the principal diagnosis for these Medicare Severity Diagnosis-Related Groups.
Informational only — actual DRG assignment also depends on procedures, complications/comorbidities (CC/MCC), discharge status, and payer-specific rules not reflected here.