Hereditary retinal dystrophy

H7_HEREDRETINADYST

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 H35.5
Hospital discharge: ICD-9 3627
Cause of death: ICD-10 H35.5
Cause of death: ICD-9 3627

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

431

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Check minimum number of events None

431

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Include endpoints None

431

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Remove individuals based on genotype QC

409

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H7_HEREDRETINADYST

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 H35
Name in latin Dystrophia retinae hereditaria

Summary Statistics

Key figures

All Female Male
Number of individuals 409 214 195
Unadjusted prevalence (%) 0.10 0.09 0.11
Mean age at first event (years) 47.04 46.66 47.46

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

Index endpoint: H7_HEREDRETINADYST – Hereditary retinal dystrophy
GWS hits: 11

Survival analyses between endpoints

Plot

before Hereditary retinal dystrophy
after Hereditary retinal dystrophy

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Hereditary retinal dystrophy

Endpoint not on priority list, no data to show.