D68.1
Billable codeHereditary factor XI deficiency
The ICD-10 code for hereditary factor xi deficiency is D68.1.
Clinical notes
Also known as
Alternate wording, synonyms, or specific conditions that fall under this code, listed to help confirm you've picked the right one.
- Hemophilia C
- Plasma thromboplastin antecedent [PTA] deficiency
- Rosenthal's disease
Documentation support
General coding-documentation guidance — not a substitute for payer-specific requirements or professional coding judgment.
- •As a general rule, code to the highest level of specificity supported by the documentation in the medical record.
Related codes in this category
- D68.0Von Willebrand diseasenon-billable header
- D68.2Hereditary deficiency of other clotting factors
- D68.3Hemorrhagic disorder due to circulating anticoagulantsnon-billable header
- D68.4Acquired coagulation factor deficiency
- D68.5Primary thrombophilianon-billable header
- D68.6Other thrombophilianon-billable header
- D68.8Other specified coagulation defects
- D68.9Coagulation defect, unspecified
- D68.1Hereditary factor XI deficiency
ICD-9-CM equivalent
Informational only — GEM mappings are approximate, not guaranteed one-to-one equivalents. Verify before use in billing.
- 2862
Associated MS-DRGs
D68.1 can serve as the principal diagnosis for these Medicare Severity Diagnosis-Related Groups.
Informational only — actual DRG assignment also depends on procedures, complications/comorbidities (CC/MCC), discharge status, and payer-specific rules not reflected here.