Pyoderma gangrenosum

pyoderma gangrenosum: ['An idiopathic, rapidly evolving, and severely debilitating disease occurring most commonly in association with chronic ulcerative colitis. It is characterized by the presence of boggy, purplish ulcers with undermined borders, appearing mostly on the legs. The majority of cases are in people between 40 and 60 years old. Its etiology is unknown.']

Endpoint definition

FinnGen phenotype data
diagram bullet diagram downward connector

Filter registries Inpat., Oupat., Death

Hospital Discharge: ICD-10 L88
Cause of death: ICD-10 L88

Check pre-conditions None

Include endpoints None

Check conditions None

Apply sex-specific rule None

diagram downward connector L12_PYODERMAGANGRENOSUM

Extra metadata

Level in the ICD hierarchy 3
First used in FinnGen datafreeze DF2
Parent code in ICD-10 L80-L99
Name in latin Pyoderma gangraenosum

Summary Statistics

Key figures

All Female Male
Number of individuals 81 50 31
Unadjusted prevalence (%) 0.03 0.03 0.03
Mean age at first event (years) 51.61 49.78 54.56

Mortality

Follow-up Absolute risk HR [95% CI] p N
1998–2019 - - - -
15 years - - - -
5 years - - - -
1 year - - - -

Correlations

Index endpoint: L12_PYODERMAGANGRENOSUM – Pyoderma gangrenosum
GWS hits: 0

Survival analyses between endpoints

Plot

before Pyoderma gangrenosum
after Pyoderma gangrenosum

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Drugs most likely to be purchased after Pyoderma gangrenosum