- D68.2 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2024 edition of ICD-10-CM D68.2 became effective on October 1, 2022.
- This is the American ICD-10-CM version of D68.2 – other international versions of ICD-10 D68.2 may differ.
ICD-10-CM D68.2 is grouped within Diagnostic Related Group(s):
- 813 Coagulation disorders
Applicable To
- 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
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2016 (effective 10/1/2015): No change
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2024 (effective 10/1/2022): No change
Diagnosis Index entries containing back-references to D68.2:
- fibrinogen (congenital) > Absence (of) (organ or part) (complete or partial)
- congenital > Afibrinogenemia D68.8
- hereditary NEC > coagulation (factor) D68.9
- fibrin polymerization > Defect, defective Q89.9
- Hageman (factor) > Defect, defective Q89.9
- accelerator globulin (Ac G) (blood) > Deficiency, deficient
- AC globulin (congenital) (hereditary) > Deficiency, deficient
- activating factor (blood) > Deficiency, deficient
- autoprothrombin > Deficiency, deficient
- I > autoprothrombin D68.2
- C > autoprothrombin D68.2
- clotting factor NEC (hereditary) > Deficiency, deficient
- clotting factor NEC > coagulation NOS D68.9
- contact factor > Deficiency, deficient
- factor > Deficiency, deficient
- Hageman > factor D68.2
- I (congenital) (hereditary) > factor D68.2
- II (congenital) (hereditary) > factor D68.2
- V (congenital) (hereditary) > factor D68.2
- VII (congenital) (hereditary) > factor D68.2
- X (congenital) (hereditary) > factor D68.2
- XII (congenital) (hereditary) > factor D68.2
- XIII (congenital) (hereditary) > factor D68.2
- fibrin-stabilizing factor (congenital) (hereditary) > Deficiency, deficient
- fibrinase > Deficiency, deficient
- fibrinogen (congenital) (hereditary) > Deficiency, deficient
- glass factor > Deficiency, deficient
- Hageman factor > Deficiency, deficient
- labile factor (congenital) (hereditary) > Deficiency, deficient
- Laki-Lorand factor > Deficiency, deficient
- proaccelerin (congenital) (hereditary) > Deficiency, deficient
- proconvertin factor (congenital) (hereditary) > Deficiency, deficient
- prothrombin (congenital) (heredItary) > Deficiency, deficient
- Prower factor > Deficiency, deficient
- SPCA (factor VII) > Deficiency, deficient
- stable factor (congenital) (hereditary) > Deficiency, deficient
- Stuart-Prower (factor X) > Deficiency, deficient
- thrombokinase > Deficiency, deficient
- Hageman (congenital factor XII deficiency) > Disease, diseased
- Stuart-Prower (congenital factor X deficiency) > Disease, diseased
- Stuart\’s (congenital factor X deficiency) > Disease, diseased
- congenital > Fibrinogenopenia D68.8
- congenital (hereditary) > Hypofibrinogenemia D68.8
- Owren\’s > Syndrome