Hereditary retinal dystrophy

DOID MESH PheWeb

H7_HEREDRETINADYST

No definition available.

Endpoint definition

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FinnGen phenotype data

321302 individuals

Apply sex-specific rule None

321302

Check conditions None

321302

Filter registries

Hospital Discharge: ICD-10 H35.5

Hospital discharge: ICD-9 3627

Hospital discharge: ICD-8 $!$

Cause of death: ICD-10 H35.5

Cause of death: ICD-9 3627

Cause of death: ICD-8 $!$

315

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

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

315

Check minimum number of events None

315

Include endpoints None

315

H7_HEREDRETINADYST

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

Similar endpoints

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List of similar endpoints to Hereditary retinal dystrophy based on the number of shared cases.

Broader endpoints:

Narrower endpoints:

None

Show all endpoint correlations

Summary Statistics

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Key figures

	All	Female	Male
Number of individuals	296	144	152
Unadjusted prevalence (%)	0.10	0.08	0.11
Mean age at first event (years)	46.47	46.98	45.98

Mortality

Follow-up	Absolute risk	HR [95% CI]	p	N
1998–2019	0.04	2.97 [1.29, 6.82]	1.0e-2	22
15 years	0.01	2.08 [0.85, 5.12]	1.1e-1	15
5 years	-	-	-	-
1 year	-	-	-	-

Age distribution of first events

Year distribution of first events

Cumulative Incidence

Correlations

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Index endpoint: H7_HEREDRETINADYST – Hereditary retinal dystrophy
GWS hits: 7

Survival analyses between endpoints

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Plot

before Hereditary retinal dystrophy
after Hereditary retinal dystrophy

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Table

Loading survival analyses table

Drugs most likely to be purchased after Hereditary retinal dystrophy

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