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81174 - chromosome inactivation) gene analysis; known familial variant

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Procedure / Servicechromosome inactivation) gene analysis; known familial variant
Procedure / Service Description

for attenuation correction and anatomical localization imaging; limited area (eg, chest, - 81173 chromosome inactivation) gene analysis; full gene sequence AR (androgen receptor) (eg, spinal and bulbar muscular atrophy, Kennedy disease, X 81174 chromosome inactivation) gene analysis; known familial variant ASXL1 (additional sex combs like 1, transcriptional regulator) (eg, myelodysplastic syndrome, myeloproliferative neoplasms, chronic myelomonocytic leukemia), gene analysis; full gene

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.