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Chorioretinal inflammation

DOID EFO MESH SNOMED PheWeb

H7_CHORIORETINFLAM

pars planitis: Form of granulomatous uveitis occurring in the region of the pars plana. This disorder is a common condition with no detectable focal pathology. It causes fibrovascular proliferation at the inferior ora serrata.

Endpoint definition

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FinnGen phenotype data

356077 individuals

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Apply sex-specific rule None

356077

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Check conditions None

356077

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Filter registries

Hospital Discharge: ICD-10 H30, H32.0*, H32.0*A18.5, H32.0*A52.79, H32.0*A69.2, H32.0*B58.0
Hospital discharge: ICD-9 363[0-2]
Hospital discharge: ICD-8 365|36700
Cause of death: ICD-9 363[0-2]
Cause of death: ICD-8 365|36700

1770

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Check pre-conditions, main-only, mode, ICD version

Look only at ICD versions H.D: 10, 8, 9 ; C.O.D: 10, 8, 9

669

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Check minimum number of events None

669

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Include endpoints None

669

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H7_CHORIORETINFLAM

Extra metadata

Level in the ICD hierarchy 3
First used in FinnGen datafreeze DF6

Summary Statistics

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Key figures

All Female Male
Number of individuals 669 394 275
Unadjusted prevalence (%) 0.19 0.20 0.17
Mean age at first event (years) 46.20 44.37 48.83

Mortality

Follow-up Absolute risk HR [95% CI] p N
1998–2019 0.02 1.04 [0.40, 2.70] 9.3e-1 61
15 years 0.01 0.73 [0.29, 1.81] 4.9e-1 24
5 years 0.00 2.22 [0.94, 5.23] 6.9e-2 17
1 year 0.00 7.81 [3.26, 18.73] 4.1e-6 11

Age distribution of first events

Year distribution of first events

Cumulative Incidence

Correlations

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Index endpoint: H7_CHORIORETINFLAM – Chorioretinal inflammation
GWS hits:

Survival analyses between endpoints

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Plot

before Chorioretinal inflammation
after Chorioretinal inflammation

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Chorioretinal inflammation

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