M35.2 Behçet's diseaseBillable ICD-10-CM code, FY2026. Acts as a Complication or Comorbidity (CC) as a secondary diagnosis.
Defines the logic of DRG(s) 545-547 in MDC 08.
136.1 Behcet's syndrome (approximate)136.1 Behcet's syndrome (approximate)711.20 Arthropathy in Behcet's syndrome, site unspecified (approximate)M02 Postinfective and reactive arthropathies ("Behçet's disease (M35.2)")M45 Ankylosing spondylitis ("Behçet's disease (M35.2)")N77.0 Ulceration of vulva in diseases classified elsewhere ("Behçet's disease (M35.2)")I77 Other disorders of arteries and arterioles ("collagen (vascular) diseases (M30-M36)")J82 Pulmonary eosinophilia, not elsewhere classified ("pulmonary eosinophilia due to systemic connective tissue disorders (M30-M36)")J84.170 Interstitial lung disease with progressive fibrotic phenotype in diseases classified elsewhere ("systemic connective tissue disorders (M30-M36)")L94 Other localized connective tissue disorders ("systemic connective tissue disorders (M30-M36)")M35.0A Sjogren syndrome with glomerular diseaseM35.0B Sjogren syndrome with vasculitisM35.0C Sjogren syndrome with dental involvementM35.09 Sjogren syndrome with other organ involvementM35.1 Other overlap syndromesM35.2 Behcet's disease (this code)M35.3 Polymyalgia rheumaticaM35.4 Diffuse (eosinophilic) fasciitisM35.5 Multifocal fibrosclerosisM35.6 Relapsing panniculitis [Weber-Christian]M35.7 Hypermobility syndrome