ICD-10-CM 2027 diagnosis code
D68.2Hereditary deficiency of other clotting factors
D68.2 is a valid, billable ICD-10-CM code for hereditary deficiency of other clotting factors. It can be reported on claims for dates of service from October 1, 2026 – September 30, 2027.
Looking up by condition? See ICD-10 code for Fibrinopenia, ICD-10 code for Parahemophilia, ICD-10 code for Dysfibrinogenemia, ICD-10 code for Hypoprothrombinemia.
Code unchanged since ICD-10-CM took effect on October 1, 2015. Source: official FY2027 ICD-10-CM release from CDC/NCHS and CMS. Page updated September 29, 2026. About our data
About D68.2
D68.2 is the ICD-10-CM diagnosis code for hereditary deficiency of other clotting factors. It belongs to category D68 (other coagulation defects), block D65-D69 (coagulation defects, purpura and other hemorrhagic conditions) and chapter 3 (diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism). It is billable, so it can be reported on its own for dates of service from October 1, 2026 through September 30, 2027.
Within D68, choose D68.2 (Hereditary deficiency of other clotting factors) only when documentation doesn't support a more specific option: von Willebrand disease (D68.0), hereditary factor XI deficiency (D68.1), hemorrhagic disorder due to circulating anticoagulants (D68.3), acquired coagulation factor deficiency (D68.4), primary thrombophilia (D68.5), other thrombophilia (D68.6), other specified coagulation defects (D68.8) and coagulation defect, unspecified (D68.9).
As a secondary diagnosis it is a CC (complication or comorbidity), which can move an inpatient stay into the "with CC" MS-DRG of its family, unless the principal diagnosis excludes it.
In MS-DRG v44.0, it is part of the grouping logic for DRG 813 (Coagulation Disorders, relative weight 1.5257), in MDC 16 (Diseases and Disorders of the Blood and Blood Forming Organs and Immunological Disorders), as a principal or secondary diagnosis. The DRG a claim lands in depends on the principal diagnosis, procedures and any CC/MCC secondary diagnoses.
It has been part of ICD-10-CM since the code set took effect on October 1, 2015 and hasn't changed since.
Before ICD-10, this condition was coded in ICD-9-CM as 286.3 (congenital deficiency of other clotting factors).
Coding notes
- 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
Notes that apply from higher levels
Instructions written at a parent level also apply to D68.2.
Broader instructions also apply from Chapter 3: Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism.
Alphabetic index entries
40 entriesTerms in the official ICD-10-CM index that lead to D68.2.
- Absence (of) (organ or part) (complete or partial) › fibrinogen (congenital)
- Afibrinogenemia › congenital
- Defect, defective › coagulation (factor) › hereditary NEC
- Defect, defective › fibrin polymerization
- Defect, defective › Hageman (factor)
- Deficiency, deficient › accelerator globulin (Ac G) (blood)
- Deficiency, deficient › AC globulin (congenital) (hereditary)
- Deficiency, deficient › activating factor (blood)
- Deficiency, deficient › autoprothrombin › I
- Deficiency, deficient › autoprothrombin › C
- Deficiency, deficient › clotting factor NEC (hereditary)
- Deficiency, deficient › coagulation NOS › clotting factor NEC
- Deficiency, deficient › contact factor
- Deficiency, deficient › factor › Hageman
- Deficiency, deficient › factor › I (congenital) (hereditary)
- Deficiency, deficient › factor › II (congenital) (hereditary)
- Deficiency, deficient › factor › V (congenital) (hereditary)
- Deficiency, deficient › factor › VII (congenital) (hereditary)
- Deficiency, deficient › factor › X (congenital) (hereditary)
- Deficiency, deficient › factor › XII (congenital) (hereditary)
- Deficiency, deficient › factor › XIII (congenital) (hereditary)
- Deficiency, deficient › 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
- Disease, diseased › Hageman (congenital factor XII deficiency)
- Disease, diseased › Stuart-Prower (congenital factor X deficiency)
- Disease, diseased › Stuart's (congenital factor X deficiency)
- Dysfibrinogenemia (congenital)
MS-DRG v44.0 grouping
All DRGs →Inpatient MS-DRGs this diagnosis can group to, as the principal or a secondary diagnosis, depending on the rest of the claim.
MDC 16 · Diseases and Disorders of the Blood and Blood Forming Organs and Immunological Disorders
ICD-9-CM equivalent
Converter →- 286.3Congenital deficiency of other clotting factorsexact
From the CMS 2018 General Equivalence Mappings (GEMs), the final GEMs release.
Code history
- 2016
- 2017
- 2018
- 2019
- 2020
- 2021
- 2022
- 2023
- 2024
- 2025
- 2026
- 2027
- FY2016 (effective 10/1/2015): Added (first year of ICD-10-CM)
- No changes since FY2016.
Common questions about D68.2
Is D68.2 billable?
- Yes. D68.2 is a billable/specific ICD-10-CM code valid for FY2027 (October 1, 2026 – September 30, 2027).
Can D68.2 be used as a principal diagnosis?
- Yes. The Medicare Code Editor doesn't restrict D68.2 as a principal diagnosis.
Is D68.2 a CC or MCC?
- D68.2 is a CC (complication or comorbidity) under MS-DRG v44.0, unless excluded by the principal diagnosis.
What DRG does D68.2 group to?
- D68.2 is used in the MS-DRG v44.0 logic for MS-DRG 813 (Coagulation Disorders). Which one applies depends on whether it is the principal diagnosis and on the rest of the claim.
What is the ICD-9 code for D68.2?
- The CMS General Equivalence Mappings map D68.2 to ICD-9-CM 286.3.