81324 Pmp22 gene dup/delet
Pathology & Lab
Also known as: PMP22 copy number analysis, CMT1A duplication deletion test
Peripheral Myelin Protein 22 (PMP22) gene duplication and deletion analysis to identify copy number variations in Charcot-Marie-Tooth disease.
Clinical Context
Detects PMP22 duplications and deletions causing Charcot-Marie-Tooth disease type 1A, the most common inherited neuropathy.
RVU Breakdown
| Work RVU | 0.00 |
| Practice Expense RVU | 0.00 |
| Malpractice RVU | 0.00 |
| Total RVU | 0.00 |
Specialties
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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.