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
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

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

Index endpoint: L12_SCLERODACTYLY – Sclerodactyly
GWS hits:

Survival analyses between endpoints

Plot

before Sclerodactyly
after Sclerodactyly

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