- D68.4 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 D68.4 became effective on October 1, 2022.
- This is the American ICD-10-CM version of D68.4 – other international versions of ICD-10 D68.4 may differ.
ICD-10-CM D68.4 is grouped within Diagnostic Related Group(s):
- 813 Coagulation disorders
Applicable To
- Deficiency of coagulation factor due to liver disease
- Deficiency of coagulation factor due to vitamin K deficiency
Type 1 Excludes
- vitamin K deficiency of newborn (P53)
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 D68.4:
- acquired > coagulation (factor) D68.9
- due to > coagulation (factor) D68.9
- liver disease > due to D68.4
- vitamin K deficiency > due to D68.4
- acquired > AC globulin (congenital) (hereditary) D68.2
- acquired (any) > coagulation NOS D68.9
- due to > coagulation NOS D68.9
- hyperprothrombinemia > due to D68.4
- liver disease > due to D68.4
- vitamin K deficiency > due to D68.4
- acquired > multiple (congenital) D68.8
- acquired > fibrin-stabilizing factor (congenital) (hereditary) D68.2
- acquired > labile factor (congenital) (hereditary) D68.2
- acquired > proaccelerin (congenital) (hereditary) D68.2
- acquired > proconvertin factor (congenital) (hereditary) D68.2
- acquired > prothrombin (congenital) (heredItary) D68.2
- acquired > stable factor (congenital) (hereditary) D68.2
- acquired > Fibrinopenia (hereditary) D68.2
- calcipriva > Hemophilia (classical) (familial) (hereditary) D66
- nonfamilial > Hemophilia (classical) (familial) (hereditary) D66
- acquired > Hypoprothrombinemia (congenital) (hereditary) (idiopathic) D68.2