Congenital malformations of oesophagus

DOID PheWeb

Q17_CONGEN_MALFO_OESOPHAGUS

No definition available.

Endpoint definition

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FinnGen phenotype data

321302 individuals

Apply sex-specific rule None

321302

Check conditions None

321302

Filter registries

Hospital Discharge: ICD-10 Q39

Cause of death: ICD-10 Q39

Check pre-conditions, main-only, mode, ICD version

Look only at ICD versions H.D: 10 ; C.O.D: 10

Check minimum number of events None

Include endpoints None

Q17_CONGEN_MALFO_OESOPHAGUS

Extra metadata

Level in the ICD hierarchy 3

First used in FinnGen datafreeze DF4

Parent code in ICD-10 Q3[8-9]|Q4[0-5]

Name in latin Malformationes congenitae oesophagi

Similar endpoints

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List of similar endpoints to Congenital malformations of oesophagus based on the number of shared cases.

Broader endpoints:

Narrower endpoints:

None

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Summary Statistics

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Key figures

	All	Female	Male
Number of individuals	79	36	43
Unadjusted prevalence (%)	0.03	0.02	0.03
Mean age at first event (years)	45.91	43.34	48.06

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: Q17_CONGEN_MALFO_OESOPHAGUS – Congenital malformations of oesophagus
GWS hits:

Survival analyses between endpoints

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Plot

before Congenital malformations of oesophagus
after Congenital malformations of oesophagus

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Table

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Drugs most likely to be purchased after Congenital malformations of oesophagus

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