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

321302 individuals

diagram downward connector

Apply sex-specific rule None

321302

diagram downward connector

Check conditions None

321302

diagram downward connector
diagram bullet

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 $!$

116

diagram downward connector
diagram bullet

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

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

116

diagram downward connector

Check minimum number of events None

116

diagram downward connector

Include endpoints None

116

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 112 64 48
Unadjusted prevalence (%) 0.04 0.04 0.04
Mean age at first event (years) 55.18 55.00 55.42

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: 0

Survival analyses between endpoints

Plot

before Dermatopolymyositis, unspecified
after Dermatopolymyositis, unspecified

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Dermatopolymyositis, unspecified