Other congenital malformations

DOID MESH PheWeb

No definition available.

Endpoint definition

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FinnGen phenotype data

Filter registries Inpat., Oupat., Death

Hospital Discharge: ICD-10 Q80-Q89

Cause of death: ICD-10 Q80-Q89

Check pre-conditions None

Include endpoints

Q17_CONGEN_ICHTHYOSIS

Q17_EPIDERMOL_BULLOSA

Q17_OTHER_CONGEN_MALFO_SKIN

Q17_CONGEN_MALFO_BREAST

Q17_OTHER_CONGEN_MALFO_INTEG

Q17_PHAKOMATOSES_NOT_ELSEW_CLASSIFIED

Q17_CONGEN_MALFO_SYNDR_KNOWN_EXOGE_CAUSES_NOT_ELSEW_CLASSIFIED

Q17_OTHER_SPECIFE_CONGEN_MALFO_SYNDR_AFFECTING_MULTIPLE_SYSTEMS

Q17_OTHER_CONGEN_MALFO_NOT_ELSEW_CLASSIFIED

Check conditions None

Apply sex-specific rule None

Q17_OTHER_CONGEN_MALFO

Extra metadata

Level in the ICD hierarchy 2

First used in FinnGen datafreeze DF4

Parent code in ICD-10 Q

Name in latin Aliae malformationes congenitae

Similar endpoints

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List of similar endpoints to Other congenital malformations based on the number of shared cases.

Broader endpoints:

Narrower endpoints:

Show all endpoint correlations

Summary Statistics

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Key figures

	All	Female	Male
Number of individuals	1578	1063	515
Unadjusted prevalence (%)	0.61	0.72	0.46
Mean age at first event (years)	36.61	36.02	37.84

Mortality

Follow-up	Absolute risk	HR [95% CI]	p	N
1998–2019	0.03	2.00 [0.79, 5.04]	1.4e-1	70
15 years	0.02	2.59 [1.27, 5.29]	9.1e-3	57
5 years	0.00	3.66 [1.88, 7.14]	1.4e-4	19
1 year	-	-	-	-

Correlations

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Index endpoint: Q17_OTHER_CONGEN_MALFO – Other congenital malformations
GWS hits: 0

Survival analyses between endpoints

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Plot

before Other congenital malformations
after Other congenital malformations

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Table

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Drugs most likely to be purchased after Other congenital malformations

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