This is a non-core endpoint: only basic statistics are computed.
Aortic arch syndrome [Takayasu]
DOID EFO MESH SNOMED Endpoint Browser
M13_TAKAYASU
Takayasu arteritis: Takayasu arteritis (TAK) is a rare inflammatory large-vessel vasculitis primarily affecting the aorta and its major branches, but also other large vessels, causing stenosis, occlusion, or aneurysm.
Endpoint definition
↥429209 individuals
Apply sex-specific rule None
429209
Check conditions None
429209
Check pre-conditions, main-only, mode, registry filters
2 out of 7 registries used, show all original rules.
51
Check minimum number of events None
51
Include endpoints None
51
Remove individuals based on genotype QC
49
Control definitions
Extra metadata
Show upset plot detailing case counts by codes
Or the full data table
Similar endpoints
↥List of similar endpoints to Aortic arch syndrome [Takayasu] based on the number of shared cases.
Broader endpoints:
- Other necrotizing vasculopathies (FG)
- Other necrotizing vasculopathies
- Systemic connective tissue disorders
- Autoimmune diseases related-to ILD
- Finngen Rheumatological endpoints
Narrower endpoints:
None
Summary Statistics
↥Key figures
All | Female | Male | |
---|---|---|---|
Number of individuals | 49 | 37 | 12 |
Unadjusted prevalence (%) | 0.01 | 0.02 | 0.01 |
Mean age at first event (years) | 46.37 | 48.35 | 40.29 |
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_TAKAYASU – Aortic arch syndrome [Takayasu]
GWS hits:
Survival analyses between endpoints
↥Not a core endpoint, no data to show.
Drugs most likely to be purchased after Aortic arch syndrome [Takayasu]
↥Endpoint not on priority list, no data to show.