This is a non-core endpoint: only basic statistics are computed.
See these related core endpoints for full statistics:
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
392423 individuals
Apply sex-specific rule None
392423
Check conditions None
392423
Check pre-conditions, main-only, mode, registry filters
2 out of 7 registries used, show all original rules.
403
Check minimum number of events None
403
Remove individuals based on genotype QC
421
M13_DERMATOPOLY
Control definitions
Control exclude
M13_SYSTCONNECT
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
Show upset plot detailing case counts by codes
Or the full data table
Similar endpoints
↥List of similar endpoints to
Dermatopolymyositis
based on the number of shared cases.
Broader endpoints:
- Systemic connective tissue disorders
- Autoimmune diseases related-to ILD
- Immune disease comorbidities
- Immune disease comorbidities
- Autoimmune diseases
Narrower endpoints:
Summary Statistics
↥Key figures
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 421 | 263 | 158 |
| Unadjusted prevalence (%) | 0.11 | 0.12 | 0.10 |
| Mean age at first event (years) | 51.71 | 50.57 | 53.60 |
Mortality
Not a core endpoint, no data to show.
Age distribution of first events
Year distribution of first events
Cumulative Incidence
Not a core endpoint, no data to show.
Correlations
↥
Index endpoint: M13_DERMATOPOLY – Dermatopolymyositis
GWS hits:
Survival analyses between endpoints
↥Not a core endpoint, no data to show.
Drugs most likely to be purchased after Dermatopolymyositis
↥Endpoint not on priority list, no data to show.