Dermatopolymyositis, unspecified

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

Endpoint definition

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FinnGen phenotype data
diagram bullet diagram downward connector

Filter registries Inpat., Oupat., Death

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

Check pre-conditions None

Include endpoints None

Check conditions None

Apply sex-specific rule None

diagram downward connector M13_DERMATOPOLYNAS

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

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Key figures

All Female Male
Number of individuals 90 51 39
Unadjusted prevalence (%) 0.03 0.03 0.03
Mean age at first event (years) 56.63 56.34 57.00

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: M13_DERMATOPOLYNAS – Dermatopolymyositis, unspecified
GWS hits: 0

Survival analyses between endpoints

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Plot

before Dermatopolymyositis, unspecified
after Dermatopolymyositis, unspecified

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Dermatopolymyositis, unspecified

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