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Dermatopolymyositis, unspecified

DOID EFO MESH SNOMED PheWeb

M13_DERMATOPOLYNAS

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 M33.9
Hospital discharge: ICD-9 $!$
Hospital discharge: ICD-8 $!$
Cause of death: ICD-10 M33.9
Cause of death: ICD-9 $!$
Cause of death: ICD-8 $!$

135

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

Look only at ICD versions H.D: 10, 8, 9 ; C.O.D: 10, 8, 9

135

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Check minimum number of events None

135

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Include endpoints None

135

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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 135 78 57
Unadjusted prevalence (%) 0.04 0.04 0.04
Mean age at first event (years) 54.77 54.84 54.66

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_DERMATOPOLYNAS – Dermatopolymyositis, unspecified
GWS hits:

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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