Athena Diagnostics - Testing that Makes a Difference
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Hypercholesterolemia Evaluation #895
Type of Disorder: Cholesterol
Typical Presentation: Elevated plasma levels of total cholesterol and plasma LDL-cholesterol, tendon xanthomata, premature coronary heart disease (CHD)
Indications for Testing: Elevated plasma cholesterol levels
Family history of premature CHD
Family history of hypercholesterolemia
Disease(s) tested for: Familial Hypercholesterolemia
Test Details
Test Code: 895
Profile includes: APOB (Hypercholesterolemia) Mutation Analysis, LDLR (Hypercholesterolemia) DNA Sequencing Test
Informed Consent Required: Yes
Medicare ABN Required: Yes
Technical Information
Utility: Detects mutations (including point mutations, deletions, insertions, and rearrangements) in the coding sequence of LDLR and in the region of APOB where all disease associated mutations have been found
Methodology: Polymerase Chain Reaction (PCR), DNA sequencing of entire protein coding region of gene
Reference Value: No mutation 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(19), 83904(19), 83909(1), 83912(1)
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: Yellow or lavender top
Stability: Hemolysis may compromise DNA recovery and integrity after 48 hrs
Storage Conditions: For short periods (until shipped) at 4°C
Shipping Conditions: Overnight at room temperature (specimen arrival must be less than 24 hrs after collection); ship Monday through Thursday only
Test Turnaround: 2 - 8 weeks
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