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

Apply sex-specific rule None

321302

Check conditions None

321302

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

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

Check minimum number of events None

116

Include endpoints None

116

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

Similar endpoints

↥

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

Broader endpoints:

Narrower endpoints:

None

Show all endpoint correlations

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 survival analyses plot

Table

Loading survival analyses table

Drugs most likely to be purchased after Dermatopolymyositis, unspecified

↥