81326 Pmp22 gene known fam variant
Also known as: PMP22 familial variant testing, CMT family screening
Peripheral Myelin Protein 22 (PMP22) gene analysis for known familial variants in Charcot-Marie-Tooth disease.
In Plain Language
Family CMT genetic test; Inherited neuropathy screening
Clinical Context
Targeted PMP22 testing of family members for previously identified variants in Charcot-Marie-Tooth disease families.
RVU Information
CPT 81326 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 81326?
CPT 81326 (Pmp22 gene known fam variant) is a Pathology & Lab code. Peripheral Myelin Protein 22 (PMP22) gene analysis for known familial variants in Charcot-Marie-Tooth disease.
Who uses CPT code 81326?
CPT 81326 is used by Pathology, Neurology, Genetics. Targeted PMP22 testing of family members for previously identified variants in Charcot-Marie-Tooth disease families.
When is CPT 81326 used?
Targeted PMP22 testing of family members for previously identified variants in Charcot-Marie-Tooth disease 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.