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Dermatopolymyositis

DOID EFO MESH SNOMED PheWeb

M13_DERMATOPOLY

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

356077 individuals

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Apply sex-specific rule None

356077

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Check conditions None

356077

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Filter registries

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

358

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Check pre-conditions, main-only, mode, ICD version

Look only at ICD versions H.D: 10 ; C.O.D: 10

358

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Check minimum number of events None

358

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Include endpoints

387

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M13_DERMATOPOLY

Extra metadata

Level in the ICD hierarchy 3
First used in FinnGen datafreeze DF2
Parent code in ICD-10 M30-M36
Name in latin Dermato[poly]myositis

Summary Statistics

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Key figures

All Female Male
Number of individuals 387 243 144
Unadjusted prevalence (%) 0.11 0.12 0.09
Mean age at first event (years) 51.08 50.04 52.84

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

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Index endpoint: M13_DERMATOPOLY – Dermatopolymyositis
GWS hits:

Survival analyses between endpoints

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Plot

before Dermatopolymyositis
after Dermatopolymyositis

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Dermatopolymyositis

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