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0269U - of 14 genes, blood, buccal swab, or amniotic fluid

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Procedure / Serviceof 14 genes, blood, buccal swab, or amniotic fluid
Procedure / Service Description

Rare constitutional and other heritable disorders, identification of copy number variations, - 0269T programming, and repositioning, when performed) Hematology (autosomal dominant congenital thrombocytopenia), genomic sequence analysis 0269U of 14 genes, blood, buccal swab, or amniotic fluid Revision or removal of carotid sinus baroreflex activation device; lead only, unilateral (includes 0270T intra-operative interrogation, programming, and repositioning, when performed)

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.