Relapsing polychondritis

relapsing polychondritis: Relapsing polychondritis (RP) is a rare, clinically heterogeneous, multisystemic inflammatory disease characterized by inflammation of the cartilage and proteoglycan rich structures leading to cartilage damage with joint, ocular and cardiovascular involvement.

Endpoint definition

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FinnGen phenotype data
diagram bullet diagram downward connector

Filter registries Inpat., Oupat., Death

Hospital Discharge: ICD-10 M94.1
Cause of death: ICD-10 M94.1

Check pre-conditions None

Include endpoints None

Check conditions None

Apply sex-specific rule None

diagram downward connector M13_RELAPSPOLYCHONDR

Extra metadata

Level in the ICD hierarchy 4
First used in FinnGen datafreeze DF2
Parent code in ICD-10 M94
Name in latin Polychondritis recidiva

Summary Statistics

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Key figures

All Female Male
Number of individuals 36 25 11
Unadjusted prevalence (%) 0.01 0.02 0.01
Mean age at first event (years) 51.83 50.39 55.11

Mortality

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

Correlations

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Index endpoint: M13_RELAPSPOLYCHONDR – Relapsing polychondritis
GWS hits:

Survival analyses between endpoints

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Plot

before Relapsing polychondritis
after Relapsing polychondritis

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Relapsing polychondritis

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