This is a non-core endpoint: only basic statistics are computed.
Sclerodactyly
DOID EFO MESH SNOMED Endpoint Browser
L12_SCLERODACTYLY
connective tissue disease: A disorder characterized by abnormalities in one or more of the elements of the connective tissues, typically associated with genetic defects.
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.
9
Check minimum number of events None
9
Include endpoints None
9
Remove individuals based on genotype QC
9
L12_SCLERODACTYLY
Control definitions
Control exclude
L12_OTHERSKINSUBCUTIS
Extra metadata
Level in the ICD hierarchy
4
First used in FinnGen datafreeze
DF2
Parent code in ICD-10
L94
Name in latin
Sclerodactylia
Not enough data for upset plot.
Or the full data table
Similar endpoints
↥List of similar endpoints to
Sclerodactyly
based on the number of shared cases.
Broader endpoints:
- Other localized connective tissue disorders
- Other disorders of skin and subcutaneous tissue
- Diseases of the skin and subcutaneous tissue
- Genitourinary diseases
- Diseases of the musculoskeletal system and connective tissue
Narrower endpoints:
None
Summary Statistics
↥Key figures
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 9 | 6 | - |
| Unadjusted prevalence (%) | 0.00 | 0.00 | - |
| Mean age at first event (years) | 52.12 | 48.99 | - |
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: L12_SCLERODACTYLY – Sclerodactyly
GWS hits:
Survival analyses between endpoints
↥Not a core endpoint, no data to show.
Drugs most likely to be purchased after Sclerodactyly
↥Endpoint not on priority list, no data to show.