Dermatopolymyositis, unspecified

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
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

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

Index endpoint: M13_DERMATOPOLYNAS – Dermatopolymyositis, unspecified
GWS hits: 0

Survival analyses between endpoints

Plot

before Dermatopolymyositis, unspecified
after Dermatopolymyositis, unspecified

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Drugs most likely to be purchased after Dermatopolymyositis, unspecified