Welcome to PathemaGX
We Provide Comprehensive Genetic Testing Services For Both Individuals And Healthcare Providers.
We Provide Comprehensive Genetic Testing Services For Both Individuals And Healthcare Providers.
We give patients the genetic information they need to achieve a healthier, more enjoyable life.
Offering health care professionals a full suite of diagnostic-testing across multiple clinical specialties.
We uncover your genetic information to enable more effective preventative care, personalized treatment regimens and greater clinical knowledge overall.
By utilizing today’s most advanced molecular testing techniques, PathemaGx can identify specific pathogens through their unique gene expressions.
Easy to do with just 5 simple steps
Open package and remove collector without touching sponge tip. Place sponge as far back in your mouth as you feel comfortable then gently rub along your lower gums in a back-and-forth motion 10 times (see close-up image). If possible, avoid rubbing your teeth.
Gently repeat rubbing motion on the opposite side of your mouth along your lower gums 10 more times.
Hold the tube upright to prevent the liquid inside the tube from spilling. Unscrew the blue cap from the collection tube without touching the sponge.
Turn the cap upside down, then insert the sponge into the tube and close cap tightly.
Invert the capped tube and shake vigorously 10 times. That’s all there is to it!
As a leading molecular-diagnostics laboratory, we partner with clinicians by offering a full suite of genetics-testing capabilities. These not only help maximize a clinical provider’s ability to accurately and timely diagnose and treat patients’ medical conditions, they also give patients the knowledge of their unique, specific genetic makeup so they can take effective actions in response.
PathemaGx is proud to be a CLIA-certified and CAP-accredited clinical molecular laboratory that serves all 50 states. We were founded on the principles of true partnership in medication safety and compliance. We’re fully committed to upholding the industry’s highest standards of service and strictest regulatory compliance in providing clinically relevant data to providers and patients.
Knowing your family history is an important first step, but testing can give you a more accurate picture of your risk for a hereditary cardiovascular disease. This helps you and your healthcare professional understand your risk so you can make the best choices for preventive care.
Testing for a hereditary cardiovascular disease will enable you and your doctor to inform other members of your family about their risk of inheriting heart disease. This information can permit both you and family members make the best choices for preventive care.
While testing is the most accurate way to determine the risk of hereditary cardiovascular disease, only people who have heart disease in their family or their personal history need to be tested. If you have heart disease and/or it runs in your family, let your healthcare professional know.
To determine if you could benefit from genetic testing for hereditary heart disease, simply take the simple 30-second Pathema GX Labs quiz. It will give you the information you need to discuss your risk of heart disease with your healthcare professional and to request further evaluation
First, ask your healthcare professional if testing is right for you. If so and if approved by your doctor, your genetic-testing kit will be sent to you by Priority Mail. Simply follow instructions on how to use the enclosed noninvasive Q-tip oral swab, then mail back your DNA specimen in the pre-paid package.
The results will be sent to your trusted healthcare professional within 2-3 weeks of the day your sample arrives at the lab.
Most insurance carriers cover genetic-testing services for hereditary cardiovascular disease. Although each case is unique, the average patient pays little to nothing out of pocket.
If you have any questions about partnership opportunities to meet your testing-services needs or any other questions, we welcome your inquiry.
Knowing your family history is an important first step, but testing for a hereditary cancer risk gives you and your healthcare professional a more accurate picture of your risk, which enables the best choices to be made for preventive care.
Testing for a hereditary cancer reveals your risk for developing a second primary cancer, thus helping your doctor determine the best type of preventive care. You can then make your family members aware of their hereditary risk as well.
While testing is the most accurate way to determine your risk of hereditary cancer, if you have had cancer and/or cancer runs in your family, your primary physician may already direct or recommend that you get tested so that such health professional has a better understanding of any other potential health risks you may have.
To decide if you might benefit from hereditary-cancer genetic testing, simply take the simple, 30-second Pathema GX Labs quiz. Based on the results, you can discuss your risk of cancer with your healthcare professional and ask for further evaluation.
First, ask your healthcare professional if testing is right for you. If so, and if approved by your doctor, your genetic testing kit will be sent to you by Priority Mail. Simply follow instructions on how to use the enclosed noninvasive Q-tip oral swab, then mail back your DNA specimen in the pre-paid package.
The results will be sent to your trusted healthcare professional within 2-3 weeks of the day your sample arrives at the lab.
The results will be sent to your healthcare professional. Pathema GX labs can, however, give you (along with your physician) access to the education portal, which will help you understand the results. In many cases, a genetic counselor is provided if ordered by your doctor.
Most insurance carriers cover genetic-testing services for hereditary cancer. Although each case is unique, the average patient pays little to nothing out of pocket.
Knowing your family history is an important first step, but testing can give you a more accurate picture of your risk for a hereditary cardiovascular disease. This helps you and your healthcare professional understand your risk so you can make the best choices for preventive care.
Testing for a hereditary cardiovascular disease will enable you and your doctor to inform other members of your family about their risk of inheriting heart disease. This information can permit both you and family members make the best choices for preventive care.
While testing is the most accurate way to determine the risk of hereditary cardiovascular disease, only people who have heart disease in their family or their personal history need to be tested. If you have heart disease and/or it runs in your family, your primary physician may already direct or recommend that you get tested so that such health professional has a better understanding of any other potential health risks you may have.
To determine if you could benefit from genetic testing for hereditary heart disease, simply take the simple 30-second Pathema GX Labs quiz. It will give you the information you need to discuss your risk of heart disease with your healthcare professional and to request further evaluation.
First, ask your healthcare professional if testing is right for you. If so and if approved by your doctor, your genetic-testing kit will be sent to you by Priority Mail. Simply follow instructions on how to use the enclosed noninvasive Q-tip oral swab, then mail back your DNA specimen in the pre-paid package.
The results will be sent to your trusted healthcare professional within 2-3 weeks of the day your sample arrives at the lab.
Most insurance carriers cover genetic-testing services for hereditary cardiovascular disease. Although each case is unique, the average patient pays little to nothing out of pocket.
Pharmacogenomics is the study of how your genes affect your response to drugs. This relatively new field combines pharmacology (the science of drugs) and genomics (the study of genes and their functions) to develop effective, safe medications and doses that are tailored to your unique genetic makeup.
Ask your healthcare professional if pharmacogenomics testing is right for you. If so, and if approved by your doctor, your genetic-testing kit will be sent to you by Priority Mail. Simply follow instructions on how to use the enclosed noninvasive Q-tip oral swab, then mail back your DNA specimen in the pre-paid package.
The results will be sent to your trusted healthcare professional within 2-3 weeks of the day your sample arrives at the lab.
The results will be sent to your healthcare professional. Pathema GX labs can, however, give you (along with your physician) access to the education portal, which will help you understand the results. In many cases, a genetic counselor is provided if ordered by your doctor.
Most insurance carriers cover genetic-testing services for pharmacogenomics. Although each case is unique, the average patient pays little to nothing out of pocket.