D68.2
ICD-10BillableHereditary deficiency of other clotting factors
Official ICD-10-CM descriptor (FY2026)
Hereditary deficiency of other clotting factors
D68.2 is valid for submission on a claim — CMS flags it as a billable, specific code.
Inclusion terms
- 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
Related codes in D68
- D68.0Von Willebrand diseasecategory
- D68.1Hereditary factor XI deficiency
- D68.3Hemorrhagic disorder due to circulating anticoagulantscategory
- D68.4Acquired coagulation factor deficiency
- D68.5Primary thrombophiliacategory
- D68.6Other thrombophiliacategory
- D68.8Other specified coagulation defects
- D68.9Coagulation defect, unspecified
Where this code sits
- Parent code
- D68
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ICD-10-CM FY2026. Centers for Medicare & Medicaid Services (CMS) / National Center for Health Statistics (NCHS), “2026 ICD-10-CM Code Descriptions in Tabular Order” (icd10cm_order_2026.txt). Download the original file from cms.gov. Public domain (US Government work). Descriptors, billable flags and instructional notes on this page are reproduced from that file without modification. Krasyn adds no clinical guidance.