Conditions / Genetic
familial renal glucosuria
info · Genetic · ICD-10: E74.818
A renal glycosuria that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the SLC5A2 gene on chromosome 16p11.2.
Signs and symptoms
- Polydipsia
- Polyphagia
- Glycosuria
- Polyuria
- Enuresis nocturna
Also known as: FRG; SGLT2 deficiency; familial renal glycosuria; hereditary renal glycosuria