81250 G6pc gene
Also known as: G6PC gene testing, Glycogen Storage Disease 1a screening
Molecular analysis of the G6PC gene to identify mutations associated with Glycogen Storage Disease type 1a.
In Plain Language
metabolic disorder gene test; genetic hypoglycemia screening
Clinical Context
Used to diagnose Glycogen Storage Disease type 1a in infants with severe hypoglycemia and hepatomegaly.
RVU Information
CPT 81250 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 81250?
CPT 81250 (G6pc gene) is a Pathology & Lab code. Molecular analysis of the G6PC gene to identify mutations associated with Glycogen Storage Disease type 1a.
Who uses CPT code 81250?
CPT 81250 is used by Genetics, Pediatrics, Pathology. Used to diagnose Glycogen Storage Disease type 1a in infants with severe hypoglycemia and hepatomegaly.
When is CPT 81250 used?
Used to diagnose Glycogen Storage Disease type 1a in infants with severe hypoglycemia and hepatomegaly.
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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.