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81413 - Genetic Testing Cardiac ion channelopathies (eg, Brugada syndrome, long QT
This procedure appears on the selected insurer prior authorization source.
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Procedure / ServiceGenetic Testing Cardiac ion channelopathies (eg, Brugada syndrome, long QT
Procedure / Service Description
Canavan disease, cystic fibrosis, familial dysautonomia, Fanconi - and SMPD1 Genetic Testing 81413 Cardiac ion channelopathies (eg, Brugada syndrome, long QT syndrome, short QT syndrome, catecholaminergic polymorphic
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.