Familial Renal Hypouricemia due to Tubular Hypersecretion
Fanconi syndrome +
Gitelman syndrome
Hypomagnesemia, Hypertension, and Hypercholesterolemia, Mitochondrial
HYPOMAGNESEMIA, SEIZURES, AND INTELLECTUAL DISABILITY +
hypophosphatemic nephrolithiasis/osteoporosis 2
Hypouricemia, Hypercalcinuria, and Decreased Bone Density
iminoglycinuria
Liddle syndrome +
nephrogenic syndrome of inappropriate antidiuresis
oculocerebrorenal syndrome +
pseudohypoaldosteronism +
Renal Aminoacidurias +
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.