ICD-10-CM
ICD-10 code for Afibrinogenemia congenital: D68.2
The ICD-10-CM index points "Afibrinogenemia congenital" to D68.2, Hereditary deficiency of other clotting factors. D68.2 is a billable code.
Source: CDC ICD-10-CM FY2027 Alphabetic Index file dated June 16, 2026. Publisher page
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More specific codes in D68
A header groups codes and is not billed. A billable code is one you can report.
- D68Other coagulation defectsHeader
- D68.0Von Willebrand diseaseHeader
- D68.00Von Willebrand disease, unspecifiedBillable
- D68.01Von Willebrand disease, type 1Billable
- D68.02Von Willebrand disease, type 2Header
- D68.020Von Willebrand disease, type 2ABillable
- D68.021Von Willebrand disease, type 2BBillable
- D68.022Von Willebrand disease, type 2MBillable
- D68.023Von Willebrand disease, type 2NBillable
- D68.029Von Willebrand disease, type 2, unspecifiedBillable
- D68.03Von Willebrand disease, type 3Billable
- D68.04Acquired von Willebrand diseaseBillable
- D68.09Other von Willebrand diseaseBillable
- D68.1Hereditary factor XI deficiencyBillable
- D68.2Hereditary deficiency of other clotting factorsBillable
- D68.3Hemorrhagic disorder due to circulating anticoagulantsHeader
- D68.31Hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitorsHeader
- D68.311Acquired hemophiliaBillable
- D68.312Antiphospholipid antibody with hemorrhagic disorderBillable
- D68.318Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitorsBillable
- D68.32Hemorrhagic disorder due to extrinsic circulating anticoagulantsBillable
- D68.4Acquired coagulation factor deficiencyBillable
- D68.5Primary thrombophiliaHeader
- D68.51Activated protein C resistanceBillable
- D68.52Prothrombin gene mutationBillable
- D68.59Other primary thrombophiliaBillable
- D68.6Other thrombophiliaHeader
- D68.61Antiphospholipid syndromeBillable
- D68.62Lupus anticoagulant syndromeBillable
- D68.69Other thrombophiliaBillable
- D68.8Other specified coagulation defectsBillable
- D68.9Coagulation defect, unspecifiedBillable
Excludes1
Excludes1 means these codes are not reported together.
From D68. A note on a category applies to every code under it.
Excludes2
Excludes2 means the other condition can be reported with this one when both are documented.
From D68. A note on a category applies to every code under it.
Related conditions
Related pages
- D68.2 code detailsNotes, nearby codes, CMS-HCC group
- Category D68Every code under it
- Chapter 3Diseases of the blood and blood-forming organs
- ICD-10 codes by conditionA to Z
- Check a list of ICD-10 codes
- Denial code CO-11Diagnosis does not support the procedure
- Denial code CO-146Diagnosis invalid for the date of service
- HCPCS Level II code lookup
Questions
What is the ICD-10 code for Afibrinogenemia congenital?
The ICD-10-CM index points "Afibrinogenemia congenital" to D68.2, Hereditary deficiency of other clotting factors. D68.2 is a billable code.
Is D68.2 billable?
Yes. D68.2 is a billable code in the FY2027 ICD-10-CM file. Use a more specific code when the record documents one.
What documentation notes apply to D68.2?
The CDC tabular list gives 1 Excludes1 note (not coded together), 2 Excludes2 notes (may be coded together when both are documented) for D68.2 and the categories above it. They are listed on this page.
What chapter is D68.2 in?
Chapter 3. Diseases of the blood and blood-forming organs.
When do ICD-10-CM codes change?
Every October 1, with the new fiscal year file. Some years add April 1 updates. This page uses the FY2027 file, effective October 1, 2026.