Term Name: familial renal glucosuria
Synonyms: familial renal glycosuria, FRG, hereditary renal glycosuria, SGLT2 deficiency
Definition: A renal glycosuria that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the SLC5A2 gene on chromosome 16p11.2.
Ontology: Human Disease [DOID:0070613]   ( DOID:0070613 )

Relationships
is a type of: autosomal dominant disease autosomal recessive disease renal glycosuria