This is a non-core endpoint: only basic statistics are computed.
Linear scleroderma
DOID EFO MESH Endpoint Browser
L12_LINEARSCLERODERMA
scleroderma: Scleroderma is a rare autoimmune connective tissue disorder characterized by abnormal hardening of the skin and, sometimes, other organs. It is classified into two main forms: localized scleroderma and systemic sclerosis (SSc), the latter comprising three subsets; diffuse cutaneous SSc (dcSSc), limited cutaneous SSc (lcSSc) and limited SSc (lSSc) (see these terms).
Endpoint definition
↥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.
30
Check minimum number of events None
30
Include endpoints None
30
Remove individuals based on genotype QC
29
Control definitions
Extra metadata
Show upset plot detailing case counts by codes
Or the full data table
Similar endpoints
↥List of similar endpoints to Linear scleroderma 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
- Any operation in hilmo
- Any event in hilmo or specialist outpatient
Narrower endpoints:
None
Summary Statistics
↥Key figures
All | Female | Male | |
---|---|---|---|
Number of individuals | 29 | 22 | 7 |
Unadjusted prevalence (%) | 0.01 | 0.01 | 0.00 |
Mean age at first event (years) | 38.88 | 37.09 | 44.52 |
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_LINEARSCLERODERMA – Linear scleroderma
GWS hits:
Survival analyses between endpoints
↥Not a core endpoint, no data to show.
Drugs most likely to be purchased after Linear scleroderma
↥Endpoint not on priority list, no data to show.