4A62 Behçet disease
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
Behçet disease is a disease of incompletely understood aetiopathogenesis characterised by recurrent oral and/or genital aphthous ulcers accompanied by cutaneous, ocular, articular, gastrointestinal, and/or central nervous system inflammatory lesions. Small vessel vasculitis, thrombotic vasculopathy, arteritis and arterial aneurysms may occur. It has a high prevalence from the Eastern Mediterranean across Central Asia to China and Japan.
inclusions
- Adamantiades-Behçet disease
code elsewhere
synonyms
- Behçet disease
- Adamantiades-Behçet disease
- Mucocutaneous Behçet disease
- Oropharyngeal ulceration due to Behçet disease
- Anogenital ulceration due to Behçet disease
- Ulceration of vulva due to Behçet disease
- Ulceration of penis or scrotum due to Behçet disease
- Penile or scrotal ulceration due to Behçet disease
- Cutaneous manifestations of Behçet disease
- Ocular Behçet disease
- Behçet arthritis
- Gastrointestinal complications of Behçet disease
- Primary ulcer of small intestine in Behçet disease
- Cardiovascular complications of Behçet disease
- Neurological complications of Behçet disease
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