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81326 - PMP22 (peripheral myelin protein 22) (eg, Charcot-Marie-Tooth, hereditary

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Procedure / ServicePMP22 (peripheral myelin protein 22) (eg, Charcot-Marie-Tooth, hereditary
Procedure / Service Description

Genetic and Molecular Testing Medical Necessity Guideline - 81325 PMP22 (peripheral myelin protein 22) (eg, Charcot-Marie-Tooth, hereditary neuropathy with liability to pressure palsies) gene analysis; full sequence analysis 81326 PMP22 (peripheral myelin protein 22) (eg, Charcot-Marie-Tooth, hereditary neuropathy with liability to pressure palsies) gene analysis; known familial variant 81327 SEPT9 (Septin9) (eg, colorectal cancer) promoter methylation analysis

Likely documents
  • Confirm benefit details
  • Submit clinical notes if requested by the plan
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  • Confirm the current plan policy before submission.
  • Use the insurer authorization workflow for this listed code.