Atrophoderma of Pasini and Pierini

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

321302 individuals

Apply sex-specific rule None

321302

Check conditions None

321302

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 $!$

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

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

Check minimum number of events None

Include endpoints None

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

Similar endpoints

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List of similar endpoints to Atrophoderma of Pasini and Pierini 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	11	8	-
Unadjusted prevalence (%)	0.00	0.00	-
Mean age at first event (years)	43.79	43.49	-

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

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Table

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

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