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This is a non-core endpoint: only basic statistics are computed.

Benign neoplasm: Oesophagus

Endpoint Browser

CD2_BENIGN_OESOPHAGUS_EXALLC

Endpoint definition

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Endpoint definition steps

FinnGen

Phenotype data

1. Apply sex-specific rule

None

-

2. Check conditions

None

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

Registry filters:

  • Hospital discharge: ICD-10 — D13.0&
  • Hospital discharge: ICD-9 — 2110
  • Hospital discharge: ICD-8 — 2110
  • Cause of death: ICD-10 — D13.0&
  • Cause of death: ICD-9 — 2110
  • Cause of death: ICD-8 — 2110

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

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4. Check minimum number of events

None

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5. Include endpoints

None

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6. Filter based on genotype QC (FinnGen only)

None

-

Control definitions (FinnGen only)

Control exclude C3_CANCER, C3_CANCER_WIDE

Extra metadata

Level in the ICD hierarchy 3
First used in FinnGen datafreeze DF2
Parent code in ICD-10 D13
Name in latin Neoplasma benignum oesophagi

Case counts by codes

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FinnGen case counts by registry codes:

No upset plot: script not run.

No upset table: script not run.

Summary Statistics

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-FinRegistry-

This endpoint is excluded from FinRegistry analyses (omitted endpoint).

-FinnGen-

Key figures

All Female Male
Number of individuals 366 193 173
Unadjusted period prevalence (%) 0.08 0.08 0.09
Median age at first event (years) 60.88 58.60 63.43

-FinnGen-

Age distribution of first events

-FinnGen-

Year distribution of first events

-FinnGen-

Cumulative Incidence Function

Not a core endpoint, no data to show.

Mortality – FinRegistry

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This endpoint is excluded from FinRegistry analyses (omitted endpoint).

Relationships between endpoints

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Index endpoint: CD2_BENIGN_OESOPHAGUS_EXALLC – Benign neoplasm: Oesophagus

GWS hits: -

This endpoint is excluded from FinRegistry analyses (omitted endpoint).