This is a non-core endpoint: only basic statistics are computed.
Endpoint definition
↥
FinnGen phenotype data
429209 individuals
Apply sex-specific rule None
429209
Check conditions None
429209
Check pre-conditions, main-only, mode, registry filters
2 out of 7 registries used, show all original rules.
6
Check minimum number of events None
6
Include endpoints None
6
Remove individuals based on genotype QC
6
Q17_CONGEN_ECTRO
Control definitions
Controls for this endpoint are individuals that are not cases.
Extra metadata
First used in FinnGen datafreeze
DF6v3
Not enough data for upset plot.
Not enough data for upset table.
Similar endpoints
↥List of similar endpoints to
Congenital ectropion
based on the number of shared cases.
Broader endpoints:
- Congenital malformations of eyelid, lacrimal apparatus and orbit
- Congenital malformations of eye, ear, face and neck
- Congenital malformations, deformations and chromosomal abnormalities
- Factors influencing health status and contact with health services
- Any operation in hilmo
Narrower endpoints:
None
Summary Statistics
↥Key figures
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 6 | - | - |
| Unadjusted prevalence (%) | 0.00 | - | - |
| Mean age at first event (years) | 28.70 | - | - |
Mortality
Not a core endpoint, no data to show.
Age distribution of first events
Year distribution of first events
Cumulative Incidence
Not a core endpoint, no data to show.
Correlations
↥
Index endpoint: Q17_CONGEN_ECTRO – Congenital ectropion
GWS hits:
Survival analyses between endpoints
↥Not a core endpoint, no data to show.
Drugs most likely to be purchased after Congenital ectropion
↥Endpoint not on priority list, no data to show.