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This is a non-core endpoint: only basic statistics are computed.

Linear scleroderma

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

FinnGen phenotype data

429209 individuals

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Apply sex-specific rule None

429209

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Check conditions None

429209

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Check pre-conditions, main-only, mode, registry filters

Hospital Discharge: ICD-10 L94.1
Cause of death: ICD-10 L94.1

2 out of 7 registries used, show all original rules.

30

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Check minimum number of events None

30

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Include endpoints None

30

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Remove individuals based on genotype QC

29

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L12_LINEARSCLERODERMA

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 Scleroderma lineare

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.