No. The symptom checker helps you track and communicate your symptoms clearly but does not diagnose conditions.

It can help identify the underlying cause of symptoms affecting multiple systems, enabling earlier and more targeted care.

Ask your doctor about referral to a neurology, nephrology, cardiology, or genetics department, or a national centre specialising in inherited metabolic diseases.

Multi-system diseases can mimic many more common conditions. Symptoms like fatigue, pain, or digestive problems are often treated separately — without recognising they might share the same root cause. People also adapt to chronic discomfort, assuming their symptoms are “normal” or just part of ageing. For rare or inherited conditions, even healthcare professionals may not immediately suspect a genetic link.

These renowned centres provide comprehensive genetic and metabolic care:
1. Ann & Robert H. Lurie Children’s Hospital of Chicago
2. Northwestern Medicine Clinical Genetics & Genomics (Feinberg School of Medicine)

At Volv Global, we combine advanced AI in healthcare with real-world data (RWD) to deliver transformative solutions for rare and difficult-to-diagnose disease patients. Our proprietary methodology for machine learning in healthcare technology enables: – Detecting rare diseases faster and more accurately – Generating real-world evidence (RWE) for clinical trials and regulatory submissions – Optimising the patient journey with data-driven insights – Reducing time and costs in drug development and market access By partnering with Volv Global, pharmaceutical innovators, healthcare providers, and policymakers gain the tools to make smarter, faster, and more impactful decisions across the entire healthcare ecosystem.