This is a non-core endpoint: only basic statistics are computed.
See these related core endpoints for full statistics:
This is a non-core endpoint: only basic statistics are computed.
See these related core endpoints for full statistics:
H7_CHORDYSTROPTHY
No definition available.
Endpoint definition steps |
FinnGen |
---|---|
Phenotype data |
429209 |
1. Apply sex-specific ruleNone |
429209 |
2. Check conditionsNone |
429209 |
3. Check pre-conditions, main-only, mode, registry filtersRegistry filters:
2 out of 7 registries used, show all original rules. |
27 |
4. Check minimum number of eventsNone |
27 |
5. Include endpointsNone |
27 |
6. Filter based on genotype QC (FinnGen only) |
25 |
Control definitions (FinnGen only)
Extra metadata
List of similar endpoints to Hereditary choroidal dystrophy based on the number of shared cases.
Broader endpoints:
Narrower endpoints:
None
All | Female | Male | |
---|---|---|---|
Number of individuals | |||
Whole population | 353 | 147 | 204 |
Only index persons | 326 | 139 | 187 |
Unadjusted period prevalence (%) | |||
Whole population | 0.01 | 0.00 | 0.01 |
Only index persons | 0.01 | 0.01 | 0.01 |
Median age at first event (years) | |||
Whole population | 49.47 | 52.15 | 47.46 |
Only index persons | 47.61 | 50.70 | 45.32 |
All | Female | Male | |
---|---|---|---|
Number of individuals | 25 | 13 | 12 |
Unadjusted period prevalence (%) | 0.01 | 0.01 | 0.01 |
Median age at first event (years) | 52.29 | 48.10 | 56.84 |
Not a core endpoint, no data to show.
Index endpoint: H7_CHORDYSTROPTHY – Hereditary choroidal dystrophy
GWS hits: -
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