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Monogenic Hypertension Evaluation #749
Type of Disorder: Monogenic Hypertension
Typical Presentation: Early onset of hypertension in the presence of a strong family associated with low plasma renin activity (PRA)
Indications for Testing: Early onset of hypertension, low plasma renin activity (PRA), low aldosterone
Disease(s) tested for: Congenital Adrenal Hyperplasia, Pseudohypoaldosteronism Type 1, Liddle's syndrome, Apparent Mineralocorticoid Excess (AME), Monogenic Hypertension
Test Details
Test Code: 749
Profile includes: SCNN1B DNA Sequencing Test, SCNN1G DNA Sequencing Test, CYP11B1 DNA Sequencing Test, HSD11B2 DNA Sequencing Test
Informed Consent Required: Yes
Technical Information
Utility: Detects mutations in the SCNN1B, SCNN1G, CYP11B1, and HSD11B2 genes
Methodology: DNA sequencing
Reference Value: No sequence variation detected
CPT Coding
The CPT codes provided are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.
Stacked CPT Code(s): 83891(1), 83898(38), 83904(38), 83909(38), 83912(1)
CPT 2013: 81404(1), 81405(1), 81406(2)
Shipping Considerations
Please label each specimen tube with two forms of patient identification. These forms of identification must also appear on the requisition form.
Preferred Specimen Requirements
Type: Whole blood
Minimum Volume: 10 ml (Pediatric minimum: 2 ml)
Collection Tube: Lavender top (EDTA)
Stability: Hemolysis may compromise DNA recovery and integrity after 48 hrs
Storage Conditions: Refrigerate
Shipping Conditions: Ship room temperature, avoid freezing
Test Turnaround: 6-8 weeks
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