Behçet's disease (BD) is a chronic multi-systemic disorder that commonly presents with diverse clinical manifestations. These can range from inflammatory mucocutaneous lesions to serious internal organ disorders, such as gastrointestinal (GI) disease, neurologic disease, and vascular disease. 1 A number of previous studies have described the clinical manifestations of BD in patients from different geographic regions across the world, including Turkey, Iran, Japan, China, and England. However, the heterogeneity of these reports in regards to epidemiologic data, combined with the use of multiple diagnostic criteria, has limited clinicians' ability to utilize these data for aiding the prediction of disease progress and possible systemic involvement. 2,3 In particular, because infrequent, but fatal, systemic symptoms, such as neurological, GI, and vessel involvement, often precede mucocutaneous or ocular manifestations, it is difficult to predict the occurrence of these minor but severe symptoms in BD patients. [4][5][6][7] Here, to address these limitations, we analyzed the clinical manifestations in a cohort of full-blown BD patients, defined as having complete BD based on the Japanese criteria, 8 which automatically fulfill all other diagnostic criteria for BD, including the International Criteria for Behçet's disease (ICBD) 9 and the International Study Group (ISG) criteria. 1 We then performed unbiased clustering analysis to better understand the heterogeneous spectrum within complete BD, followed by subgroup analysis based on the identified clusters and logistic regression to uncover possible associations between various clinical factors and disease outcome. Critically, we anticipate that this approach will aid in the understanding of clinical outcomes in full-blown BD patients, which may ultimately explain the heterogeneity of this complex disease.