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81413 - Cardiac ion channelopathies (eg, Brugada syndrome, long QT syndrome, short QT

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Procedure / ServiceCardiac ion channelopathies (eg, Brugada syndrome, long QT syndrome, short QT
Procedure / Service Description

Genetic and Molecular Testing Medical Necessity Guideline - disease), genomic sequence analysis panel, must include sequencing of at least 9 genes, including ASPA, BLM, CFTR, FANCC, GBA, HEXA, IKBKAP, MCOLN1, and SMPD1 81413 Cardiac ion channelopathies (eg, Brugada syndrome, long QT syndrome, short QT syndrome, catecholaminergic polymorphic ventricular tachycardia); genomic sequence analysis panel, must include sequencing of at least 10 genes, including

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.