Other congenital malformations

DOID MESH PheWeb

No definition available.

Endpoint definition

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Name	Q17_OTHER_CONGEN_MALFO
Long name	Other congenital malformations
Include	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
Level in the ICD-hierarchy	2
First defined in version	DF4
Latin name	Aliae malformationes congenitae

Summary Statistics

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Key figures

	All	Female	Male
Number of individuals	1309	883	426
Unadjusted prevalence (%)	0.60	0.72	0.45
Mean age at first event (years)	36.76	36.07	38.18
Case fatality at 5-years (%)	0.92	0.45	1.88

Longitudinal metrics

	All	Female	Male
Median nb. of events per indiv.	2.0	2.0	2.0
Recurrence at 6 months (%)	46.29	44.73	49.53

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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