ICD-10-CM Code For Hereditary Factor IX Deficiency: Group Overview
The International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) code group D67 includes congenital deficiencies of coagulation factor IX, covering hereditary hemophilia B and related bleeding disorders caused by factor IX defects. These ICD-10-CM diagnosis codes are used to document clinical presentations of bleeding tendency, severity of factor deficiency, and related complications such as spontaneous bleeding or postprocedural hemorrhage. Accurate coding within the ICD-10-CM D67 group supports proper claim adjudication and complete clinical documentation for appropriate reimbursement.
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ICD-10-CM D67: Hereditary Factor IX Deficiency Overview
Hereditary factor IX deficiency encompasses congenital deficiencies of coagulation factor IX that lead to bleeding diatheses, most notably hemophilia B. These diagnoses target the hematologic and coagulation system and describe inherited impairments in clotting factor production or function. Accurate coding is important for appropriate claims processing and to reflect the clinical complexity that influences treatment and resource use.