Other conditions related to polyarteritis nodosa

Polyarteritis Nodosa: ['A necrotizing vasculitis that affects medium-sized arteries, it is usually idiopathic, and may be triggered by viral infections (Hepatitis B, also others). A multisystem disease, it most commonly affects skin (nodules, livedo reticularis) and peripheral nerves; higher morbidity is associated with gastrointestinal, central nervous system, cardiac, and/or other organ involvement. Anti-neutrophil cytoplasmic antibodies (ANCA) are typically negative. [ NCI ]']

Endpoint definition

FinnGen phenotype data
diagram bullet diagram downward connector

Filter registries Inpat., Oupat., Death

Hospital Discharge: ICD-10 M30.8
Hospital discharge: ICD-9 4460C
Cause of death: ICD-10 M30.8
Cause of death: ICD-9 4460C

Check pre-conditions None

Include endpoints None

Check conditions None

Apply sex-specific rule None

diagram downward connector M13_POYARTOTH

Extra metadata

Level in the ICD hierarchy 4
First used in FinnGen datafreeze DF2
Parent code in ICD-10 M30
Name in latin Aliae condiciones polyarteritidi nodosae cognatae

Summary Statistics

Key figures

All Female Male
Number of individuals 40 28 12
Unadjusted prevalence (%) 0.02 0.02 0.01
Mean age at first event (years) 52.77 49.65 60.05

Mortality

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

Correlations

Index endpoint: M13_POYARTOTH – Other conditions related to polyarteritis nodosa
GWS hits:

Survival analyses between endpoints

Plot

before Other conditions related to polyarteritis nodosa
after Other conditions related to polyarteritis nodosa

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Drugs most likely to be purchased after Other conditions related to polyarteritis nodosa