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Hereditary choroidal dystrophy

DOID MESH PheWeb

H7_CHORDYSTROPTHY

No definition available.

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 H31.2
Hospital discharge: ICD-9 3635
Cause of death: ICD-10 H31.2
Cause of death: ICD-9 3635

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

25

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Check minimum number of events None

25

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Include endpoints None

25

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Remove individuals based on genotype QC

23

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H7_CHORDYSTROPTHY

Control definitions

Control exclude H7_CHOROIDRETINA

Extra metadata

Level in the ICD hierarchy 4
First used in FinnGen datafreeze DF2
Parent code in ICD-10 H31
Name in latin Dystrophia chorioideae hereditaria

Summary Statistics

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Key figures

All Female Male
Number of individuals 23 13 10
Unadjusted prevalence (%) 0.01 0.01 0.01
Mean age at first event (years) 51.51 44.37 60.78

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: H7_CHORDYSTROPTHY – Hereditary choroidal dystrophy
GWS hits:

Survival analyses between endpoints

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Not a core endpoint, no data to show.

Drugs most likely to be purchased after Hereditary choroidal dystrophy

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Endpoint not on priority list, no data to show.