The IntellxxDNA Clinical Decision Support Tool
With detailed discussions of over 700 SNPs and over 10,000 references, our clinical decision support software provides comprehensive, accessible medical reports and scientific explanations of specific genomic patient data. IntellxxDNA puts the world of medical genomics research and functional medicine interventions at your fingertips
What Sets Us Apart
Accuracy and Integrity of Research
Released only to licensed health care professionals, our reporting and analytics follow strict guidelines that ensure only studies with good scientific evidence and appropriate confidence levels are included. Utilizing our proprietary analytical methodology, IntellxxDNA provides clinicians with unbiased, scientifically current data reflecting potential additive risks and benefits that are clinically significant and scientifically supported.
The Convergence of Traditional, Functional and Integrative Medicine
Our personalized reports help clinicians understand gene function and explore potential prevention and intervention strategies. One key feature of our reports is our detailed discussions of potential interventions, which include elements from integrative and functional medicine as well as traditional medicine. Clinical reports are divided into health risk and benefit categories, where genomic single nucleotide polymorphisms (SNPs) are grouped to show risks and benefits. As a Clinical Decision Support Tool, IntellxxDNA gives you enough information about potential interventions, including information about supplement mechanisms, studies and dosing, so that you can truly develop informed, targeted plans.
Our Medical Overview Report arms you with the information you need as a clinician to help your patients address and reverse chronic health issues.
Society has accepted that as we age chronic illnesses such as cardiac disease, diabetes, osteoporosis and obesity are inevitable. However, when underlying contributing factors are made clear and addressed, chronic disease can generally be prevented and often reversed.
Our Medical Overview Report gives you the information you need to guide your patients toward a healthy lifestyle, and allows you to develop a personalized prevention or treatment plan. Without genomics, there is no way of knowing who is not able to make enough nitric oxide for opening the blood vessels, who cannot properly open their insulin channels to lower their blood sugar, who does not convert thyroid hormone to its active form in their brain, or who needs extra vitamin K2 in order to keep the calcium in their bones where it belongs; not in their arteries where it can contribute to heart disease. These are just some of the hundreds of pearls that can help you personalize your care. When a patient knows that your recommendation to cut down saturated fat in their diet or take curcumin to lower inflammation is a specific recommendation for them based on their genes, they are more compliant and achieve better outcomes.
The Medical Overview Report also helps you to better understand metabolic pathways related to anesthesia, iron, blood clotting factors and other nutrients, which will improve quality of life. It may even help prevent major healthcare events.
Over 300 clinically significant gene variants are analyzed and linked to research within 20 different organized topics allowing your clinician to provide a highly individualized health plan to optimize your quality of life and achieve your health goals.
Key panels focus on the following:
