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Atrophoderma of Pasini and Pierini

DOID EFO MESH SNOMED PheWeb

L12_ATROPODERMAPASINI

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

356077 individuals

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Apply sex-specific rule None

356077

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Check conditions None

356077

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Filter registries

Hospital Discharge: ICD-10 L90.3
Hospital discharge: ICD-9 7019A
Hospital discharge: ICD-8 $!$
Cause of death: ICD-10 L90.3
Cause of death: ICD-9 7019A
Cause of death: ICD-8 $!$

13

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

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

13

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Check minimum number of events None

13

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Include endpoints None

13

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L12_ATROPODERMAPASINI

Extra metadata

Level in the ICD hierarchy 4
First used in FinnGen datafreeze DF2
Parent code in ICD-10 L90
Name in latin Atrophoderma Pasini-Pierini

Summary Statistics

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Key figures

All Female Male
Number of individuals 13 10 -
Unadjusted prevalence (%) 0.00 0.01 -
Mean age at first event (years) 43.66 43.37 -

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_ATROPODERMAPASINI – Atrophoderma of Pasini and Pierini
GWS hits:

Survival analyses between endpoints

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Plot

before Atrophoderma of Pasini and Pierini
after Atrophoderma of Pasini and Pierini

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Atrophoderma of Pasini and Pierini

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