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

PheWeb

No definition available.

Endpoint definition

↥

FinnGen phenotype data

Filter registries Inpat., Oupat., Death

Hospital Discharge: ICD-10 Q86

Cause of death: ICD-10 Q86

Check pre-conditions None

Include endpoints None

Check conditions None

Apply sex-specific rule 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

↥

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

Show all endpoint correlations

Summary Statistics

↥

Key figures

	All	Female	Male
Number of individuals	18	10	8
Unadjusted prevalence (%)	0.01	0.01	0.01
Mean age at first event (years)	24.21	25.27	22.89

Mortality

Follow-up	Absolute risk	HR [95% CI]	p	N
1998–2019	-	-	-	-
15 years	-	-	-	-
5 years	-	-	-	-
1 year	-	-	-	-

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

↥

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

Loading survival analyses plot

Table

Loading survival analyses table

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

↥