Disease Risk Management
Overview
The Disease Risk Management Panel is a precision health tool that screens for genetic predispositions to a wide range of chronic, complex, and lifestyle-related conditions. With a focus on prevention, this panel helps both individuals and providers identify hidden risk factors before symptoms arise enabling early intervention and personalized care strategies. Designed for proactive healthcare, this one-time genetic screen empowers better planning for long-term health and lifestyle optimization.
What This Test Covers
This panel analyzes genetic risk markers linked to several high-impact conditions across multiple systems:
Abdominal Aortic Aneurysm
Stroke (CVA)
Type 2 Diabetes
Heart Disease
Alzheimer’s Disease (Late Onset)
Autism
Irritable Bowel Syndrome (IBS)
Endometriosis
Lupus
Nicotine Dependence
Noise-Induced Hearing Loss
Male Pattern Baldness
Lactose Intolerance
Intracranial Aneurysm
Sight Loss
Why It Matters
Many chronic diseases begin silently and progress over time. Identifying risk early allows for action before symptoms begin. This panel helps:
- Detect predispositions to high impact diseases across body systems
- Enable early preventive care, lifestyle changes, and screening protocols
- Guide targeted nutrition, diagnostics, and wellness strategies
- Support cardiologists, endocrinologists, neurologists, primary care, and wellness professionals in delivering precision-based care
- Empower patients with genetic clarity to make informed health decisions
Who Should Take This Test
This panel is ideal for:
Individuals with a family history of chronic diseases
People interested in early detection and proactive health planning
Providers aiming to personalize care for complex conditions
Adults seeking precision insights into aging, cognition, cardiovascular, or metabolic health
Wellness and functional medicine practitioners looking to integrate genomics into long-term care
What You’ll Receive
Easy-to-understand visuals that clearly highlight relative risk across each condition.
The report outlines associated genetic risk factors, possible causes, and known symptoms
Reports are digitally delivered and easily shareable through the ExtendingME Provider Portal for streamlined clinical care.
Turnaround Time
Results will be available within 4 weeks from the receipt of the sample and will be securely delivered through the Provider Portal, enabling seamless access, viewing, and sharing of reports.
Collection Method
ExtendingME kits include all necessary self-collection devices for non-invasive, at-home saliva collection, making it easy to deliver real-time, data-driven healthcare solutions without the need for lab visits
Don’t Wait for Symptoms - Get Ahead of Risk
Turn genetic insight into preventive action. Detect, manage, and reduce the risk of chronic disease before it starts.
