Behçet disease (Q44396): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Doença de Behçet é uma doença de etiopatogenia não completamente compreendida caracterizada por úlceras aftosas orais e/ou genitais recorrentes acompanhadas de lesões inflamatórias cutâneas, oculares, articulares, gastrointestinais e/ou do sistema nervoso central. Podem ocorrer vasculites de pequenos vasos, vasculopatia trombótica, arterites e aneurismas arteriais. Tem uma alta prevalência do Mediterrâneo Oriental através de toda a Ásia Central até a China e Japão.
@@ description / en / description / en @@
+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.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1668927157
@@ Property / Canonical URI: https://id.who.int/icd/entity/1668927157 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:4A62
@@ Property / CURIE: CID11:4A62 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-4A62
@@ Property / Canary Token: dki-india-4A62 / rank @@
+Normal rank
@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
+Normal rank
@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
@@ Property / Collection date @@
+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-13T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 13 August 2026 / rank @@
+Normal rank
@@ Property / Linked ICD 10 @@
+M35.2
@@ Property / Linked ICD 10: M35.2 / rank @@
+Normal rank

Latest revision as of 11:50, 13 August 2026

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.

Language	Label	Description	Also known as
default for all languages	4A62
English	Behçet disease	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.