81325 Pmp22 gene full sequence
Also known as: PMP22 full sequencing, CMT genetic test
Peripheral Myelin Protein 22 (PMP22) gene full gene sequence analysis to identify point mutations in Charcot-Marie-Tooth disease.
In Plain Language
Charcot-Marie-Tooth disease genetic test; Neuropathy genetic analysis
Clinical Context
Full PMP22 sequencing for Charcot-Marie-Tooth disease diagnosis when copy number analysis is negative.
RVU Information
CPT 81325 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 81325?
CPT 81325 (Pmp22 gene full sequence) is a Pathology & Lab code. Peripheral Myelin Protein 22 (PMP22) gene full gene sequence analysis to identify point mutations in Charcot-Marie-Tooth disease.
Who uses CPT code 81325?
CPT 81325 is used by Pathology, Neurology, Genetics. Full PMP22 sequencing for Charcot-Marie-Tooth disease diagnosis when copy number analysis is negative.
When is CPT 81325 used?
Full PMP22 sequencing for Charcot-Marie-Tooth disease diagnosis when copy number analysis is negative.
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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.