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

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

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

Index endpoint: M13_RELAPSPOLYCHONDR – Relapsing polychondritis
GWS hits:

Survival analyses between endpoints

Plot

before Relapsing polychondritis
after Relapsing polychondritis

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Relapsing polychondritis