Congenital malformation syndromes due to known exogenous causes, not elsewhere classified

Q17_CONGEN_MALFO_SYNDR_KNOWN_EXOGE_CAUSES_NOT_ELSEW_CLASSIFIED

No definition available.

Endpoint definition

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 Q86
Cause of death: ICD-10 Q86

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

37

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Check minimum number of events None

37

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Include endpoints None

37

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Remove individuals based on genotype QC

34

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Q17_CONGEN_MALFO_SYNDR_KNOWN_EXOGE_CAUSES_NOT_ELSEW_CLASSIFIED

Control definitions

Control exclude Q17_OTHER_CONGEN_MALFO

Extra metadata

Level in the ICD hierarchy 3
First used in FinnGen datafreeze DF4
Parent code in ICD-10 Q8
Name in latin Syndromata malformationum congenitarum e causis externis notis non alibi classificata

Similar endpoints

Summary Statistics

Key figures

All Female Male
Number of individuals 34 17 17
Unadjusted prevalence (%) 0.01 0.01 0.01
Mean age at first event (years) 24.21 17.37 31.06

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

Index endpoint: Q17_CONGEN_MALFO_SYNDR_KNOWN_EXOGE_CAUSES_NOT_ELSEW_CLASSIFIED – Congenital malformation syndromes due to known exogenous causes, not elsewhere classified
GWS hits:

Survival analyses between endpoints

Not a core endpoint, no data to show.

Drugs most likely to be purchased after Congenital malformation syndromes due to known exogenous causes, not elsewhere classified

Endpoint not on priority list, no data to show.