GI Comprehensive Panel

GI Comprehensive Panel Genetic Testing

The GI Comprehensive Panel is a broad-spectrum genetic test designed to detect inherited mutations linked to various gastrointestinal (GI) disorders. It evaluates multiple genes known to influence digestive tract health, helping diagnose conditions such as Crohn’s disease, ulcerative colitis, celiac disease, hereditary polyposis syndromes, and colorectal cancer predisposition. This panel supports clinicians in identifying the genetic basis of chronic or unexplained GI symptoms, enabling earlier, more accurate diagnoses and tailored treatment plans. It is particularly valuable for individuals with a personal or family history of GI diseases. Comprehensive insights from this panel can also guide preventive care and long-term health management.

Why Choose This GI Comprehensive Panel?

Choosing the GI Comprehensive Panel Genetic Testing offers a proactive and precise approach to understanding gastrointestinal health. It helps uncover the genetic causes behind chronic, unexplained, or hereditary GI conditions, allowing for earlier diagnosis and more effective, personalized treatment strategies. Unlike traditional diagnostic methods that often rely on symptoms alone, this testing provides a deeper, molecular-level insight that can reveal hidden risks before symptoms appear. It’s especially beneficial for individuals with a family history of GI disorders or those who have not responded well to standard therapies. Ultimately, it empowers informed decisions, preventive care, and improved patient outcomes.

When Is It Used?

For patients experiencing persistent abdominal pain, diarrhea, or bloating without a clear diagnosis.
When symptoms of gastrointestinal conditions appear at an unusually young age.
If there’s a known genetic predisposition to GI cancers or hereditary disorders.
In individuals with overlapping or unclear GI conditions needing precise classification.
For patients not responding to conventional therapies and requiring targeted care.
To identify at-risk individuals before the onset of symptoms for early intervention.

Who Should Consider this Genetic Testing?

This genetic testing is ideal for individuals who have persistent or unexplained gastrointestinal symptoms that don’t respond to usual treatments. It’s especially important for those with a family history of GI disorders, hereditary cancers, or early-onset digestive diseases. Patients with multiple GI conditions or those seeking personalized treatment options can benefit greatly. Additionally, people interested in preventive health to understand their genetic risks before symptoms arise should consider this test. Consulting a healthcare provider can help determine if this comprehensive panel is right based on personal and family medical history.

You should consider this test if:

Individuals with chronic or unexplained GI symptoms
People with a family history of GI cancers or hereditary GI diseases
Patients diagnosed with multiple or complex GI disorders
Those who have not responded to standard GI treatments
Early-onset GI disease patients
Individuals with a history of recurrent GI inflammation or autoimmune GI conditions
Patients preparing for or considering GI-related surgeries who need genetic risk assessment
Individuals seeking preventive genetic screening

How We Work

How is the Test Performed?

Our Services

Just a few of the many health issues we screen for

Crohn’s Disease

Chronic inflammatory bowel disease causing abdominal pain, diarrhea, weight loss, and malnutrition due to immune system attacking the digestive tract.

Ulcerative Colitis

Inflammatory bowel disease causing long-lasting inflammation and ulcers in the colon and rectum, leading to abdominal pain and diarrhea.

Irritable Bowel Syndrome (IBS)

Functional GI disorder with abdominal pain, bloating, and altered bowel habits without structural abnormalities.

Gastroesophageal Reflux Disease (GERD)

Chronic acid reflux causing heartburn and potential damage to esophageal lining over time.

Hereditary Nonpolyposis Colorectal Cancer

Genetic condition increasing risk of colorectal and other cancers due to DNA repair gene mutations.

Familial Adenomatous Polyposis

Inherited disorder causing hundreds to thousands of colon polyps, significantly increasing colorectal cancer risk if untreated.

Who we Are

Why Choose Us?

State-of-the-Art Digital Lab Experience

Our fully integrated E-Lab platform offers online test ordering, real-time tracking, and secure digital reporting bringing convenience and control to both physicians and patients across the country.

Advanced Diagnostic Technology

From routine blood tests to complex genetic panels, we leverage cutting-edge platforms like NGS, PCR, and AI-powered analytics for maximum accuracy and clinical relevance.

Fast Turnaround, Local Support

With lab facilities based in Florida, we ensure faster processing times and direct access to our expert team. You get timely results backed by responsive, local customer support.

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TESTS

NGS TESTING

PCR TESTING

Infectious Disease