81362 Hbb gene known fam variant
Also known as: HBB familial variant testing, hemoglobinopathy family screening
Beta-Globin (HBB) gene analysis for known familial variants to facilitate screening in sickle cell and beta thalassemia families.
In Plain Language
Family sickle cell test; Inherited hemoglobin disorder screening
Clinical Context
Targeted HBB testing of family members for previously identified variants in hemoglobinopathy families.
RVU Information
CPT 81362 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 81362?
CPT 81362 (Hbb gene known fam variant) is a Pathology & Lab code. Beta-Globin (HBB) gene analysis for known familial variants to facilitate screening in sickle cell and beta thalassemia families.
Who uses CPT code 81362?
CPT 81362 is used by Pathology, Hematology, Genetics. Targeted HBB testing of family members for previously identified variants in hemoglobinopathy families.
When is CPT 81362 used?
Targeted HBB testing of family members for previously identified variants in hemoglobinopathy families.
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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.