≡ Risteys
R8

Documentation Changelog GitHub Contact & Feedback

Juvenile dermatomyositis

DOID EFO MESH SNOMED PheWeb

M13_JUVDERMATOMYO

juvenile dermatomyositis: Juvenile dermatomyositis (JDM) is the early-onset form of dermatomyositis (DM, see this term), a systemic, autoimmune inflammatory muscle disorder, characterized by proximal muscle weakness, evocative skin lesion, and systemic manifestations.

Endpoint definition

↥
FinnGen phenotype data

356077 individuals

diagram downward connector

Apply sex-specific rule None

356077

diagram downward connector

Check conditions None

356077

diagram downward connector
diagram bullet

Filter registries

Hospital Discharge: ICD-10 M33.0
Hospital discharge: ICD-9 7103A
Hospital discharge: ICD-8 $!$
Cause of death: ICD-10 M33.0
Cause of death: ICD-9 7103A
Cause of death: ICD-8 $!$

34

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

34

diagram downward connector

Check minimum number of events None

34

diagram downward connector

Include endpoints None

34

diagram downward connector
M13_JUVDERMATOMYO

Extra metadata

Level in the ICD hierarchy 4
First used in FinnGen datafreeze DF2
Parent code in ICD-10 M33
Name in latin Dermatomyositis juvenilis

Summary Statistics

↥

Key figures

All Female Male
Number of individuals 34 21 13
Unadjusted prevalence (%) 0.01 0.01 0.01
Mean age at first event (years) 30.81 24.66 40.74

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_JUVDERMATOMYO – Juvenile dermatomyositis
GWS hits:

Survival analyses between endpoints

↥

Plot

before Juvenile dermatomyositis
after Juvenile dermatomyositis

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Juvenile dermatomyositis

↥