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.
Check pre-conditions None
Include endpoints None
Check conditions None
Apply sex-specific rule None
R18_GLYCOSURIA
Extra metadata
List of similar endpoints to
Glycosuria
based on the number of shared cases.
Broader endpoints:
Narrower endpoints:
None
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 22 | 15 | 7 |
| Unadjusted prevalence (%) | 0.01 | 0.01 | 0.01 |
| Mean age at first event (years) | 40.06 | 34.74 | 51.45 |
| Follow-up | Absolute risk | HR [95% CI] | p | N |
|---|---|---|---|---|
| 1998–2019 | - | - | - | - |
| 15 years | - | - | - | - |
| 5 years | - | - | - | - |
| 1 year | - | - | - | - |
Index endpoint: R18_GLYCOSURIA – Glycosuria
GWS hits:
before Glycosuria
after Glycosuria
Loading survival analyses plot
Loading survival analyses table
