≡ Risteys
R9

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

392423 individuals

diagram downward connector

Apply sex-specific rule None

392423

diagram downward connector

Check conditions None

392423

diagram downward connector
diagram bullet

Check pre-conditions, main-only, mode, registry filters

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

2 out of 7 registries used, show all original rules.

38

diagram downward connector

Check minimum number of events None

38

diagram downward connector

Include endpoints None

38

diagram downward connector
diagram bullet diagram downward connector

Remove individuals based on genotype QC

38

diagram downward connector
M13_JUVDERMATOMYO

Control definitions

Control exclude M13_SYSTCONNECT

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 38 23 15
Unadjusted prevalence (%) 0.01 0.01 0.01
Mean age at first event (years) 30.42 24.09 40.12

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

↥

Not a core endpoint, no data to show.

Drugs most likely to be purchased after Juvenile dermatomyositis

↥

Endpoint not on priority list, no data to show.