Six waves of structured diagnostic assessments were conducted of 168 clinic-referred 7-to 12-year-olds, over 7 years. Wave-to-wave changes in the number of conduct disorder (CD) behaviors were paralleled by correlated changes in the numbers of symptoms of oppositional defiant disorder (ODD), attentiondeficit/hyperactivity disorder (ADHD), depression, and anxiety. In addition, CD in Wave 1 predicted levels of ODD, ADHD, depression, and anxiety in later waves when initial levels of those symptoms were controlled, but only ODD in Wave 1 predicted CD in later waves when initial CD levels were controlled. These findings indicate a striking degree of dynamic comorbidity between CD and other types of psychopathology and provide an initial empirical framework for needed developmental models of comorbidity.Conduct disorder (CD) co-occurs at greater than chance levels with oppositional defiant disorder (ODD), attention-deficit/hyperactivity disorder (ADHD), anxiety disorders, and depressive disorders in both clinical and population-based samples (Angold, Costello, & Erkanli, 1999;Caron & Rutter, 1991;Lahey, Miller, Gordon, & Riley, 1999;Loeber & Keenan, 1994;Moffitt, Caspi, Rutter, & Silva, 2001). Comorbid psychopathology almost certainly contributes to the distress and functional impairment experienced by youths with CD and complicates their treatment. Moreover, theories of the origins and course of CD that do not explain its high degree of comorbidity with other types of psychopathology would be incomplete. Therefore, understanding these patterns of comorbidity is essential to understanding the fundamental nature of both CD and its comorbid conditions. Caron and Rutter (1991) and Loeber and Keenan (1994) noted the particular need for longitudinal studies of comorbidity to understand the developmental relationships among disorders. Among other things, such studies would help to determine if (a) one type of psychopathology tends to precede another in developmental time and increase the likelihood of the latter type of psychopathology, (b) whether CD and other disorders are more likely to be comorbid at particular times in development than other times, and (c) whether CD and other disorders tend to wax and wane in concert over time. Such information would provide much of the necessary empirical framework for theories of both the development of CD and its dynamic comorbidity with other disorders.