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Behçet disease

DOID EFO MESH SNOMED PheWeb

M13_BEHCET

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.

Endpoint definition

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FinnGen phenotype data

392423 individuals

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Apply sex-specific rule None

392423

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Check conditions None

392423

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Check pre-conditions, main-only, mode, registry filters

Hospital Discharge: ICD-10 M35.2
Hospital discharge: ICD-9 1361
Cause of death: ICD-10 M35.2
Cause of death: ICD-9 1361

2 out of 7 registries used, show all original rules.

88

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Check minimum number of events None

88

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Include endpoints None

88

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Remove individuals based on genotype QC

85

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M13_BEHCET

Control definitions

Control exclude M13_SYSTCONNECT

Extra metadata

Level in the ICD hierarchy 4
First used in FinnGen datafreeze DF2
Parent code in ICD-10 M35
Name in latin Morbus Behçet

Summary Statistics

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Key figures

All Female Male
Number of individuals 85 64 21
Unadjusted prevalence (%) 0.02 0.03 0.01
Mean age at first event (years) 48.19 45.99 54.90

Mortality

Follow-up Absolute risk HR [95% CI] p N
1998–2019 - - - -
15 years - - - -
5 years - - - -
1 year - - - -

Age distribution of first events

Year distribution of first events

Cumulative Incidence

Correlations

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Index endpoint: M13_BEHCET – Behçet disease
GWS hits:

Survival analyses between endpoints

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Plot

before Behçet disease
after Behçet disease

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Behçet disease

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Endpoint not on priority list, no data to show.