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

PheWeb

Q17_CONGEN_MALFO_SYNDR_KNOWN_EXOGE_CAUSES_NOT_ELSEW_CLASSIFIED

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 Q86

Cause of death: ICD-10 Q86

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_SYNDR_KNOWN_EXOGE_CAUSES_NOT_ELSEW_CLASSIFIED

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

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List of similar endpoints to Congenital malformation syndromes due to known exogenous causes, not elsewhere classified 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	23	13	10
Unadjusted prevalence (%)	0.01	0.01	0.01
Mean age at first event (years)	24.54	23.18	26.32

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

Survival analyses between endpoints

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Plot

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

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

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