Dermatopolymyositis

M13_DERMATOPOLY

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

Apply sex-specific rule None

321302

Check conditions None

321302

Filter registries

Hospital Discharge: ICD-10 M33

Cause of death: ICD-10 M33

304

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

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

304

Check minimum number of events None

304

Include endpoints

M13_JUVDERMATOMYO

M13_DERMATOMYOTH

M13_POLYMYO

M13_DERMATOPOLYNAS

331

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

Similar endpoints

↥

List of similar endpoints to Dermatopolymyositis based on the number of shared cases.

Broader endpoints:

Narrower endpoints:

Show all endpoint correlations

Summary Statistics

↥

Key figures

	All	Female	Male
Number of individuals	322	204	118
Unadjusted prevalence (%)	0.10	0.12	0.09
Mean age at first event (years)	50.81	50.07	52.09

Mortality

Follow-up	Absolute risk	HR [95% CI]	p	N
1998–2019	0.01	0.73 [0.15, 3.59]	7.0e-1	51
15 years	0.00	0.57 [0.13, 2.45]	4.5e-1	22
5 years	0.00	1.77 [0.52, 6.01]	3.6e-1	15
1 year	-	-	-	-

Age distribution of first events

Year distribution of first events

Cumulative Incidence

Correlations

↥

Index endpoint: M13_DERMATOPOLY – Dermatopolymyositis
GWS hits: 0

Survival analyses between endpoints

↥

Plot

before Dermatopolymyositis
after Dermatopolymyositis

Loading survival analyses plot

Table

Loading survival analyses table

Drugs most likely to be purchased after Dermatopolymyositis

↥