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Aortic arch syndrome [Takayasu]

DOID EFO MESH SNOMED PheWeb

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

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FinnGen phenotype data

392423 individuals

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Apply sex-specific rule None

392423

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Check conditions None

392423

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

Hospital Discharge: ICD-10 M31.4
Hospital discharge: ICD-9 4467
Cause of death: ICD-10 M31.4
Cause of death: ICD-9 4467

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

45

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Check minimum number of events None

45

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Include endpoints None

45

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Remove individuals based on genotype QC

44

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M13_TAKAYASU

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 M31
Name in latin Syndroma arcus aortae

Summary Statistics

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Key figures

All Female Male
Number of individuals 44 33 11
Unadjusted prevalence (%) 0.01 0.02 0.01
Mean age at first event (years) 45.67 46.56 43.02

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

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Index endpoint: M13_TAKAYASU – Aortic arch syndrome [Takayasu]
GWS hits:

Survival analyses between endpoints

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Plot

before Aortic arch syndrome [Takayasu]
after Aortic arch syndrome [Takayasu]

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Aortic arch syndrome [Takayasu]

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Endpoint not on priority list, no data to show.