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81437 - analysis panel, 5 or more genes, interrogation for sequence variants and copy number variants

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Procedure / Serviceanalysis panel, 5 or more genes, interrogation for sequence variants and copy number variants
Procedure / Service Description

CLRN1, GJB2, GPR98, MTRNR1, MYO7A, MYO15A, PCDH15, OTOF, SLC26A4, TMC1, - Hereditary neuroendocrine tumor-related disorders (eg, medullary thyroid carcinoma, parathyroid carcinoma, malignant pheochromocytoma or paraganglioma), genomic sequence 81437 analysis panel, 5 or more genes, interrogation for sequence variants and copy number variants Hereditary neuroendocrine tumor disorders (eg, medullary thyroid carcinoma, parathyroid carcinoma, malignant pheochromocytoma or paraganglioma); duplication/deletion 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.