Direct Payment By Patients

HNL Genomics (CTGT) offers a self pay option for patients who do not have health insurance or who choose not to use their health insurance to pay for genetic testing.

Patients may elect to pay for tests using a Visa or Mastercard credit card or by money order or bank check. Patients in the United States may also pay by personal check. Payments by patients must be submitted with the Requisition Form and specimen.  For international orders, all payments must be in U.S. dollars.

For credit card payments, patients must provide complete cardholder information on the Requisition Form and sign the form where indicated.

For check and money order payments, simply insert the check or money order in the shipping container along with the Requisition Form and specimen being sent to HNL Genomics (CTGT).

A payment plan can be offered when full payment up front cannot be completed. A period of up to 10 months can be chosen, with 10% due up front.

The American Medical Association (AMA) Current Procedural Terminology (CPT) codes published by HNL Lab Medicine are guidelines and are intended for informational purposes only. CPT coding is the exclusive responsibility of the billing entity. HNL Lab Medicine strongly recommends confirmation of CPT codes with third-party payors and/or the AMA. We assume no responsibility for billing errors due to reliance upon CPT codes provided by HNL Lab Medicine.

News

August 08, 2022

Familial hypercholesterolemia (FH)

Familial hypercholesterolemia (FH) is a genetic disorder that increases the likelihood of having coronary heart disease at a younger age. Learn about how to determine if you have hypercholesterolemia and what actions you can take to create better outcomes!

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April 11, 2022

Genome Sequencing: A Vital Tool Used in Identifying and Tracking New COVID-19 Variants

Genome sequencing is reading or decoding the complete genetic information i.e. “Genome” of an organism that is encrypted in the form of a very long string called DNA made up of 4 letters, A, T, G, and C. The genome of an organism essentially determines their physical characteristics and ...
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March 03, 2022

The Effect of Genetics on Individual Heart Health: Early Identification of FH Variations to Optimize Treatment

Test must be ordered by a Physician.

Familial hypercholesterolemia (FH) is a genetic disorder that is characterized by abnormally high blood levels of low-density lipoprotein (LDL) cholesterol, sometimes referred to as "bad cholesterol". This condition affects an estimated 1 in 250 people, and increases the likelihood of developing cardiovascular disease. In fact, FH is estimated to be the cause of 2-3% of heart attacks in individuals younger than age 60.

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October 13, 2021

CTGT.net: A New Website Experience

We've refreshed our look and feel to better meet your needs. 

CTGT's new website is not only user-friendly but also provides more advanced test search capabilities, additional methodologies, and a clean design suited for multi-platform usage.

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September 28, 2021

9 New Tests for Genetic Carrier Screening Panels

HNL Genomics (CTGT) is now offering 9 NEW tests for Genetic Carrier Screening. 
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