Structural pathology is often treated as the starting point for causal explanation. This Perspective argues that, in rare, complex, and syndromic disease trajectories, the visible lesion may instead be the residue of a prior threshold transition whose upstream route has become only partially observable. The manuscript proposes multiroute functional convergence: distinct molecular, metabolic, vascular, inflammatory, or hemorheological trajectories may enter the same vulnerable physiological territory, become constrained by shared requirements, and cross into tissue-level pathology before structural damage becomes clinically legible. This pre-structural interval is defined as functional dissonance. The central claim is that structural similarity does not imply mechanistic identity. A lesion may localize where biological failure became visible without identifying how that failure was produced. Under this framework, complex disease becomes experimentally searchable rather than merely descriptive: not by cataloguing every downstream abnormality, but by reconstructing the convergence constraints, threshold transitions, and residual route-specific signals that made pathology possible.
Nereida Guillén Azpurua (Fri,) studied this question.