Glycosuria
Description
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.
Data source
| FinnGen phenocode | R18_GLYCOSURIA |
| Hospital Discharge registry | ICD-10: R81 |
| Cause of Death registry | ICD-10: R81 |
| Level in the ICD-hierarchy | 3 |
| First defined in version | DF4 |
Key figures
| Sex | All | Female | Male |
| Number of individuals | 16 | 11 | - |
| Unadjusted prevalence (%) | 0.01 | 0.01 | - |
| Mean age at first event (years) | 39.83 | 38.25 | - |
| Case fatality at 5-years (%) | 12.5 | 0.0 | - |
Longitudinal metrics
| Sex | All | Female | Male |
| Median nb. of events per indiv. | 1 | 1 | - |
| Recurrence at 6 months (%) | - | - | - |
Associations
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