Prior Auth Required

81269 - syndrome, HbH disease), gene analysis; duplication/deletion variants

This procedure appears on the selected insurer prior authorization source.

Check another codeExplore policy data
Prior authorizationPrior Auth Required
Procedure / Servicesyndrome, HbH disease), gene analysis; duplication/deletion variants
Procedure / Service Description

zygosity in multiple birth pregnancies) (List separately in addition to code for primary - 81266 procedure) HBA1/HBA2 (alpha globin 1 and alpha globin 2) (eg, alpha thalassemia, Hb Bart hydrops fetalis 81269 syndrome, HbH disease), gene analysis; duplication/deletion variants Jak2 (Janus Kinase 2) (Eg, Myeloproliferative Disorder) Gene Analysis, P.Val617Phe (V617F) 81270 Variant

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.