Juvenile dermatomyositis

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
diagram bullet diagram downward connector

Filter registries Inpat., Oupat., Death

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

Check pre-conditions None

Include endpoints None

Check conditions None

Apply sex-specific rule None

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 27 15 12
Unadjusted prevalence (%) 0.01 0.01 0.01
Mean age at first event (years) 33.27 26.97 41.13

Mortality

Follow-up Absolute risk HR [95% CI] p N
1998–2019 - - - -
15 years - - - -
5 years - - - -
1 year - - - -

Correlations

Index endpoint: M13_JUVDERMATOMYO – Juvenile dermatomyositis
GWS hits:

Survival analyses between endpoints

Plot

before Juvenile dermatomyositis
after Juvenile dermatomyositis

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Drugs most likely to be purchased after Juvenile dermatomyositis