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Benign neoplasm: Small intestine

DOID MESH Endpoint Browser PheWeb

CD2_BENIGN_SMALL_INTESTINE

No definition available.

Endpoint definition

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FinnGen phenotype data

429209 individuals

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Apply sex-specific rule None

429209

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Check conditions None

429209

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Check pre-conditions, main-only, mode, registry filters None

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

0

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Check minimum number of events None

0

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Include endpoints

1134

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Remove individuals based on genotype QC

1094

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CD2_BENIGN_SMALL_INTESTINE

Control definitions

Controls for this endpoint are individuals that are not cases.

Extra metadata

Level in the ICD hierarchy 3
First used in FinnGen datafreeze DF2

No data for upset plot.

No data for upset table.

Similar endpoints

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List of similar endpoints to Benign neoplasm: Small intestine based on the number of shared cases.

Venn diagram with an highlighted set fully inside another set Broader endpoints:

Venn diagram with a set fully inside an highlighted set Narrower endpoints:

Show all endpoint correlations

Summary Statistics

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Key figures

All Female Male
Number of individuals 1094 616 478
Unadjusted prevalence (%) 0.27 0.27 0.26
Mean age at first event (years) 61.73 60.20 63.71

Mortality

Follow-up Absolute risk HR [95% CI] p N
1998–2019 0.08 3.85 [2.55, 5.80] 1.3e-10 182
15 years 0.01 1.97 [1.30, 3.00] 1.4e-3 80
5 years 0.00 3.35 [2.11, 5.30] 2.7e-7 56
1 year 0.00 9.62 [5.85, 15.82] 4.9e-19 31

Age distribution of first events

Year distribution of first events

Cumulative Incidence

Correlations

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Index endpoint: CD2_BENIGN_SMALL_INTESTINE – Benign neoplasm: Small intestine
GWS hits: 1

Survival analyses between endpoints

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Plot

before Benign neoplasm: Small intestine
after Benign neoplasm: Small intestine

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Drugs most likely to be purchased after Benign neoplasm: Small intestine

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Endpoint not on priority list, no data to show.