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The Common Phenotypes Hypothesis

The Common Phenotypes Hypothesis proposes that Functional Neurological Disorder (FND) may confuse common neurological presentations with a distinct disorder. Much like “dropsy” once described swelling caused by various underlying diseases, symptoms such as weakness, tremors, seizures and sensory disturbances may arise from different biological processes rather than a single disorder. The hypothesis questions whether the clinical signs used to diagnose FND identify a distinct condition or merely recognise symptom patterns shared across multiple diseases, potentially obscuring their underlying causes.

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FND Study of Nearly 600,000 Patients Reveals Different Biological Patterns Behind Different Symptoms

A major 2026 study links FND diagnoses to inherited disorders, congenital abnormalities, neurodevelopmental conditions and early-life biological factors. But are these vulnerabilities to FND, or evidence that different biological diseases produce overlapping clinical phenotypes? We examine the findings through the Common Phenotypes Hypothesis.