Dermatopolymyositis, unspecified

M13_DERMATOPOLYNAS

dermatomyositis: Dermatomyositis (DM) is a type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness.

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 M33.9
Cause of death: ICD-10 M33.9

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

157

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Check minimum number of events None

157

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Include endpoints None

157

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Remove individuals based on genotype QC

153

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M13_DERMATOPOLYNAS

Control definitions

Control exclude M13_SYSTCONNECT

Extra metadata

Level in the ICD hierarchy 4
First used in FinnGen datafreeze DF2
Parent code in ICD-10 M33
Name in latin Dermato[poly]myositis non specificata

Summary Statistics

Key figures

All Female Male
Number of individuals 153 88 65
Unadjusted prevalence (%) 0.04 0.04 0.04
Mean age at first event (years) 55.54 54.79 56.55

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: M13_DERMATOPOLYNAS – Dermatopolymyositis, unspecified
GWS hits:

Survival analyses between endpoints

Plot

before Dermatopolymyositis, unspecified
after Dermatopolymyositis, unspecified

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Drugs most likely to be purchased after Dermatopolymyositis, unspecified

Endpoint not on priority list, no data to show.