Other congenital malformations

Description

No definition available.

Data source
FinnGen phenocode Q17_OTHER_CONGEN_MALFO
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
Ontology
DOID 8433
MESH D000013

Key figures

Sex All Female Male
Number of individuals 963 655 308
Unadjusted prevalence (%) 0.55 0.66 0.41
Mean age at first event (years) 37.76 37.3 38.72
Case fatality at 5-years (%) 0.73 0.46 1.3

Longitudinal metrics

Sex All Female Male
Median nb. of events per indiv. 2 2 2
Recurrence at 6 months (%) 44.65 42.9 48.38

Associations

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