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81190 - CSTB (cystatin B) (eg, Unverricht-Lundborg disease) gene analysis; known familial variant(s)

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Procedure / ServiceCSTB (cystatin B) (eg, Unverricht-Lundborg disease) gene analysis; known familial variant(s)
Procedure / Service Description

for attenuation correction and anatomical localization imaging; limited area (eg, chest, - 81188 abnormal (eg, expanded) alleles 81189 CSTB (cystatin B) (eg, Unverricht-Lundborg disease) gene analysis; full gene sequence 81190 CSTB (cystatin B) (eg, Unverricht-Lundborg disease) gene analysis; known familial variant(s) 81191 NTRK1 (neurotrophic receptor tyrosine kinase 1) (eg, solid tumors) translocation analysis 81192 NTRK2 (neurotrophic receptor tyrosine kinase 2) (eg, solid tumors) translocation 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.