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

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FinnGen phenotype data
diagram bullet diagram downward connector

Filter registries Inpat., Oupat., Death

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

Check pre-conditions None

Include endpoints None

Check conditions None

Apply sex-specific rule None

diagram downward connector L12_SCLERODACTYLY

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

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Key figures

All Female Male
Number of individuals 9 7 -
Unadjusted prevalence (%) 0.00 0.00 -
Mean age at first event (years) 50.63 50.51 -

Mortality

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

Correlations

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Index endpoint: L12_SCLERODACTYLY – Sclerodactyly
GWS hits:

Survival analyses between endpoints

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Plot

before Sclerodactyly
after Sclerodactyly

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