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81302 - MECP2 (methyl CpG binding protein 2) (eg, Rett syndrome) gene analysis; full

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Procedure / ServiceMECP2 (methyl CpG binding protein 2) (eg, Rett syndrome) gene analysis; full
Procedure / Service Description

Genetic and Molecular Testing Medical Necessity Guideline - Lynch syndrome) of markers for mismatch repair deficiency (eg, BAT25, BAT26), includes comparison of neoplastic and normal tissue, if performed 81302 MECP2 (methyl CpG binding protein 2) (eg, Rett syndrome) gene analysis; full sequence analysis 81303 MECP2 (methyl CpG binding protein 2) (eg, Rett syndrome) gene analysis; known

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