Behcet's syndrome: Bechet disease (BD) is a chronic, relapsing, multisystemic vasculitis characterized by mucocutaneous lesions, as well as articular, vascular, ocular and central nervous system manifestations.
Filter registries Inpat., Oupat., Death
Check pre-conditions None
Include endpoints None
Check conditions None
Apply sex-specific rule None
M13_BEHCET
Extra metadata
List of similar endpoints to
Behçet disease
based on the number of shared cases.
Broader endpoints:
Narrower endpoints:
None
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 59 | 44 | 15 |
| Unadjusted prevalence (%) | 0.02 | 0.03 | 0.01 |
| Mean age at first event (years) | 48.81 | 47.27 | 53.30 |
| Follow-up | Absolute risk | HR [95% CI] | p | N |
|---|---|---|---|---|
| 1998–2019 | - | - | - | - |
| 15 years | - | - | - | - |
| 5 years | - | - | - | - |
| 1 year | - | - | - | - |
Index endpoint: M13_BEHCET – Behçet disease
GWS hits:
before Behçet disease
after Behçet disease
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