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81259 - syndrome, HbH disease), gene analysis; full gene sequence

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Procedure / Servicesyndrome, HbH disease), gene analysis; full gene sequence
Procedure / Service Description

for attenuation correction and anatomical localization imaging; limited area (eg, chest, - 81258 syndrome, HbH disease), gene analysis; known familial variant HBA1/HBA2 (alpha globin 1 and alpha globin 2) (eg, alpha thalassemia, Hb Bart hydrops fetalis 81259 syndrome, HbH disease), gene analysis; full gene sequence IKBKAP (inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex- associated protein) (eg, familial dysautonomia) gene analysis, common variants (eg,

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.