Summary

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.

All SNPs

Disease Hierarchy

Disease Interacts with Genes

Processes Associated With Trait

Pathways Associated With Trait

Symptoms Associated With Trait