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Disease Ontology Browser
familial renal glucosuria (DOID:0070613)
Alliance: disease page
Synonyms: familial renal glycosuria; FRG; hereditary renal glycosuria; SGLT2 deficiency
Alt IDs: OMIM:233100, MESH:D006030, ORDO:69076, UMLS_CUI:C3245525
Definition: A renal glycosuria that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the SLC5A2 gene on chromosome 16p11.2.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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12/10/2024
MGI 6.24 		The Jackson Laboratory