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 |
E4_CARBONAS |
| Hospital Discharge registry |
ICD-10: E748/E749, ICD-8: 271[8-9] |
| Cause of Death registry |
ICD-10: E749/E748, ICD-8: 271[8-9] |
| Level in the ICD-hierarchy |
4 |
| First defined in version |
DF2 |
Ontology