81251 Gba gene
Also known as: GBA gene testing, Gaucher disease screening
Molecular analysis of the GBA gene to identify mutations associated with Gaucher disease, a lysosomal storage disorder.
In Plain Language
genetic enzyme disorder test; lysosomal storage disease screening
Clinical Context
Used to diagnose Gaucher disease in patients with hepatosplenomegaly, bone disease, and elevated acid phosphatase.
RVU Information
CPT 81251 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 81251?
CPT 81251 (Gba gene) is a Pathology & Lab code. Molecular analysis of the GBA gene to identify mutations associated with Gaucher disease, a lysosomal storage disorder.
Who uses CPT code 81251?
CPT 81251 is used by Genetics, Hematology, Pathology. Used to diagnose Gaucher disease in patients with hepatosplenomegaly, bone disease, and elevated acid phosphatase.
When is CPT 81251 used?
Used to diagnose Gaucher disease in patients with hepatosplenomegaly, bone disease, and elevated acid phosphatase.
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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.