Mucocutaneous lymph node syndrome [Kawasaki]

mucocutaneous lymph node syndrome: Kawasaki disease (KD) is a febrile, systemic, self-limiting vasculitis affecting children and characterized by inflammation in the medium sized vessels associated with coronary arterial aneurysms (CAA) that may be life threatening when untreated. KD is the most common cause of acquired heart disease in children in developed countries and is a risk factor for ischemic heart disease in adulthood.

Endpoint definition

FinnGen phenotype data
diagram bullet diagram downward connector

Filter registries Inpat., Oupat., Death

Hospital Discharge: ICD-10 M30.3
Hospital discharge: ICD-9 4461
Cause of death: ICD-10 M30.3
Cause of death: ICD-9 4461

Check pre-conditions None

Include endpoints None

Check conditions None

Apply sex-specific rule None

diagram downward connector M13_KAWASAKI

Extra metadata

Level in the ICD hierarchy 4
First used in FinnGen datafreeze DF2
Parent code in ICD-10 M30
Name in latin Syndroma mucocutaneum lymphonodorum (Kawasaki)

Summary Statistics

Key figures

All Female Male
Number of individuals 31 19 12
Unadjusted prevalence (%) 0.01 0.01 0.01
Mean age at first event (years) 22.64 20.08 26.68

Mortality

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

Correlations

Index endpoint: M13_KAWASAKI – Mucocutaneous lymph node syndrome [Kawasaki]
GWS hits:

Survival analyses between endpoints

Plot

before Mucocutaneous lymph node syndrome [Kawasaki]
after Mucocutaneous lymph node syndrome [Kawasaki]

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Mucocutaneous lymph node syndrome [Kawasaki]