Glycosuria

R18_GLYCOSURIA

renal glycosuria: An autosomal inherited disorder due to defective reabsorption of GLUCOSE by the PROXIMAL RENAL TUBULES. The urinary loss of glucose can reach beyond 50 g/day. It is attributed to the mutations in the SODIUM-GLUCOSE TRANSPORTER 2 encoded by the SLC5A2 gene.

Endpoint definition

FinnGen phenotype data

321302 individuals

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Apply sex-specific rule None

321302

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Check conditions None

321302

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Filter registries

Hospital Discharge: ICD-10 R81
Cause of death: ICD-10 R81

32

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Check pre-conditions, main-only, mode, ICD version

Look only at ICD versions H.D: 10 ; C.O.D: 10

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Check minimum number of events None

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Include endpoints None

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R18_GLYCOSURIA

Extra metadata

Level in the ICD hierarchy 3
First used in FinnGen datafreeze DF4
Parent code in ICD-10 R8[0-2]
Name in latin Glucosuria

Summary Statistics

Key figures

All Female Male
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Number of individuals
30 21 9
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Unadjusted prevalence (%)
0.01 0.01 0.01
?
Mean age at first event (years)
39.20 31.85 56.37

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Mortality

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

Age distribution of first events

Year distribution of first events

Cumulative Incidence

Correlations

Index endpoint: R18_GLYCOSURIA – Glycosuria
GWS hits:

Survival analyses between endpoints

Plot

before Glycosuria
after Glycosuria

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