Sclerodactyly

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

392423 individuals

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Apply sex-specific rule None

392423

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Check conditions None

392423

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

Hospital Discharge: ICD-10 L94.3
Cause of death: ICD-10 L94.3

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

9

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Check minimum number of events None

9

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Include endpoints None

9

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Remove individuals based on genotype QC

9

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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

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

Follow-up Absolute risk HR [95% CI] p N
1998–2019 - - - -
15 years - - - -
5 years - - - -
1 year - - - -

Age distribution of first events

Year distribution of first events

Cumulative Incidence

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.