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This is a non-core endpoint: only basic statistics are computed.

Hereditary choroidal dystrophy

H7_CHORDYSTROPTHY

No definition available.

Endpoint definition

FinnGen phenotype data

429209 individuals

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Apply sex-specific rule None

429209

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Check conditions None

429209

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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.

27

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Check minimum number of events None

27

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Include endpoints None

27

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Remove individuals based on genotype QC

25

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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

Key figures

All Female Male
Number of individuals 25 13 12
Unadjusted prevalence (%) 0.01 0.01 0.01
Mean age at first event (years) 49.85 44.37 55.77

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: H7_CHORDYSTROPTHY – Hereditary choroidal dystrophy
GWS hits:

Survival analyses between endpoints

Not a core endpoint, no data to show.

Drugs most likely to be purchased after Hereditary choroidal dystrophy

Endpoint not on priority list, no data to show.