ICD-10-CM D67 is the diagnosis code for Hereditary factor IX deficiency. This code falls under the section "Coagulation defects, purpura and other hemorrhagic conditions" within Chapter 3 — Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89). It is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. Medical coders and healthcare providers use this code to document and classify diagnoses in electronic health records, insurance claims, and clinical databases.
Understanding where D67 sits in the ICD-10-CM classification helps ensure proper coding:
Yes, D67 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
D67 is the ICD-10-CM diagnosis code for "Hereditary factor IX deficiency". It is used by healthcare providers to classify and document this condition in medical records and insurance claims.
D67 is located in Section D65-D69 — "Coagulation defects, purpura and other hemorrhagic conditions" within Chapter 3 of the ICD-10-CM Tabular List.
Use D67 when the patients documented diagnosis matches "Hereditary factor IX deficiency" and the clinical documentation supports this level of specificity. Always verify with the latest ICD-10-CM guidelines and payer requirements.
The ICD-10-CM code for Hereditary factor IX deficiency is D67.
Yes, D67 can be used as a primary diagnosis code since it is billable and specific.
D67 is in Chapter 3 of the ICD-10-CM Tabular List.
Yes, D67 is a valid ICD-10-CM code for the 2026 fiscal year, subject to official CMS updates.