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81323 - syndrome) gene analysis; duplication/deletion variant

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Procedure / Servicesyndrome) gene analysis; duplication/deletion variant
Procedure / Service Description

zygosity in multiple birth pregnancies) (List separately in addition to code for primary - 81322 syndrome) gene analysis; known familial variant PTEN (phosphatase and tensin homolog) (eg, Cowden syndrome, PTEN hamartoma tumor 81323 syndrome) gene analysis; duplication/deletion variant PMP22 (peripheral myelin protein 22) (eg, Charcot-Marie-Tooth, hereditary neuropathy with 81324 liability to pressure palsies) gene analysis; duplication/deletion analysis

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.