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

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FinnGen phenotype data

321302 individuals

Apply sex-specific rule None

321302

Check conditions None

321302

Filter registries

Hospital Discharge: ICD-10 R81

Cause of death: ICD-10 R81

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

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

Check minimum number of events None

Include endpoints None

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

Similar endpoints

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List of similar endpoints to Glycosuria based on the number of shared cases.

Broader endpoints:

Narrower endpoints:

None

Show all endpoint correlations

Summary Statistics

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Key figures

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

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

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Index endpoint: R18_GLYCOSURIA – Glycosuria
GWS hits:

Survival analyses between endpoints

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Plot

before Glycosuria
after Glycosuria

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Table

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Drugs most likely to be purchased after Glycosuria

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