SYSTSCLE_STRICT
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).
356077 individuals
Apply sex-specific rule None
356077
Check conditions
549
Check pre-conditions, main-only, mode, ICD version None
183
Check minimum number of events None
183
Include endpoints None
183
Extra metadata
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List of similar endpoints to
Systemic sclerosis,strict definition
based on the number of shared cases.
Broader endpoints:
Narrower endpoints:
None
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 183 | 160 | 23 |
| Unadjusted prevalence (%) | 0.05 | 0.08 | 0.01 |
| Mean age at first event (years) | 54.14 | 53.93 | 55.59 |
| Follow-up | Absolute risk | HR [95% CI] | p | N |
|---|---|---|---|---|
| 1998–2019 | - | - | - | - |
| 15 years | - | - | - | - |
| 5 years | - | - | - | - |
| 1 year | - | - | - | - |
Index endpoint: SYSTSCLE_STRICT – Systemic sclerosis,strict definition
GWS hits: 1
before Systemic sclerosis,strict definition
after Systemic sclerosis,strict definition
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