81238 F9 full gene sequence
Also known as: F9 sequencing, Factor IX gene analysis
Complete sequence analysis of the F9 gene to identify mutations associated with Hemophilia B.
In Plain Language
bleeding disorder gene test; hemophilia genetic screening
Clinical Context
Used to diagnose Hemophilia B (Factor IX deficiency) in males with bleeding symptoms for genetic counseling and family carrier screening.
RVU Information
CPT 81238 does not have a physician work RVU assigned by CMS. Reimbursement for this code is determined by payer-specific fee schedules.
Billing & Documentation
Lab and pathology codes require an order from the treating provider with clinical indication. For molecular pathology and genetic testing, document the specific analytes tested and clinical rationale.
How This Code Compares
This code has a work RVU of 0.00, meaning it does not have a physician work component assigned by CMS. In the Pathology & Lab category, 94% of codes share this characteristic.
Specialties
Frequently Asked Questions
What is CPT code 81238?
CPT 81238 (F9 full gene sequence) is a Pathology & Lab code. Complete sequence analysis of the F9 gene to identify mutations associated with Hemophilia B.
Who uses CPT code 81238?
CPT 81238 is used by Genetics, Hematology, Pathology. Used to diagnose Hemophilia B (Factor IX deficiency) in males with bleeding symptoms for genetic counseling and family carrier screening.
When is CPT 81238 used?
Used to diagnose Hemophilia B (Factor IX deficiency) in males with bleeding symptoms for genetic counseling and family carrier screening.
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CPT® is a registered trademark of the American Medical Association. Data sourced from CMS Physician Fee Schedule RVU26A. Descriptions, synonyms, and clinical context are original content by RVU Edge.