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Keratosis follicularis et parafollicularis in cutem penetrans [Kyrle]

DOID EFO MESH SNOMED PheWeb

L12_KERATFOLLICULETPARA

skin disease: Any deviation from the normal structure or function of the skin or subcutaneous tissue that is manifested by a characteristic set of symptoms and signs.

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 L87.0
Hospital discharge: ICD-9 7011C
Hospital discharge: ICD-8 70112
Cause of death: ICD-10 L87.0
Cause of death: ICD-9 7011C
Cause of death: ICD-8 70112

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

16

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Check minimum number of events None

16

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Include endpoints None

16

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Remove individuals based on genotype QC

15

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L12_KERATFOLLICULETPARA

Control definitions

Control exclude L12_OTHERSKINSUBCUTIS

Extra metadata

Level in the ICD hierarchy 4
First used in FinnGen datafreeze DF2
Parent code in ICD-10 L87
Name in latin Keratosis follicularis et parafollicularis in cutem penetrans (Kyrle)

Not enough data for upset plot.

Or the full data table

Summary Statistics

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Key figures

All Female Male
Number of individuals 15 7 8
Unadjusted prevalence (%) 0.00 0.00 0.00
Mean age at first event (years) 56.29 52.24 59.84

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: L12_KERATFOLLICULETPARA – Keratosis follicularis et parafollicularis in cutem penetrans [Kyrle]
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 Keratosis follicularis et parafollicularis in cutem penetrans [Kyrle]

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Endpoint not on priority list, no data to show.