{"_id":"MONDO:0009297","_version":1,"ctd":{"chemical_related_to_disease":[{"cas_registry_number":"107-09-5","chemical_name":"2-bromoethylamine","direct_evidence":"marker/mechanism","mesh_chemical_id":"C004504","pubmed":"2918855","source":"CTD"},{"chemical_name":"5-aminoisoquinoline","direct_evidence":"therapeutic","mesh_chemical_id":"C549098","pubmed":"29599129","source":"CTD"},{"cas_registry_number":"15663-27-1","chemical_name":"Cisplatin","direct_evidence":"marker/mechanism","mesh_chemical_id":"D002945","pubmed":"29599129","source":"CTD"},{"chemical_name":"Gentamicins","direct_evidence":"marker/mechanism","mesh_chemical_id":"D005839","pubmed":"7354245","source":"CTD"},{"cas_registry_number":"87-68-3","chemical_name":"hexachlorobutadiene","direct_evidence":"marker/mechanism","mesh_chemical_id":"C001335","pubmed":"2918855","source":"CTD"},{"cas_registry_number":"7487-94-7","chemical_name":"Mercuric Chloride","direct_evidence":"marker/mechanism","mesh_chemical_id":"D008627","pubmed":"2918855","source":"CTD"},{"cas_registry_number":"1404-26-8","chemical_name":"Polymyxin B","direct_evidence":"marker/mechanism","mesh_chemical_id":"D011112","pubmed":"4292201","source":"CTD"},{"cas_registry_number":"75-55-8","chemical_name":"propyleneimine","direct_evidence":"marker/mechanism","mesh_chemical_id":"C031132","pubmed":"2918855","source":"CTD"},{"cas_registry_number":"13292-46-1","chemical_name":"Rifampin","direct_evidence":"marker/mechanism","mesh_chemical_id":"D012293","pubmed":"946666","source":"CTD"},{"cas_registry_number":"7775-11-3","chemical_name":"sodium chromate(VI)","direct_evidence":"marker/mechanism","mesh_chemical_id":"C028982","pubmed":"2918855","source":"CTD"},{"cas_registry_number":"18883-66-4","chemical_name":"Streptozocin","direct_evidence":"marker/mechanism","mesh_chemical_id":"D013311","pubmed":"11219485","source":"CTD"}],"mesh":"D006030","pathway_related_to_disease":[{"inference_gene_symbol":"SLC5A2","pathway_name":"Metabolism","react_pathway_id":"R-HSA-1430728","source":"CTD"},{"inference_gene_symbol":"SLC5A2","pathway_name":"Hexose transport","react_pathway_id":"R-HSA-189200","source":"CTD"},{"inference_gene_symbol":"SLC5A2","pathway_name":"Transmembrane transport of small molecules","react_pathway_id":"R-HSA-382551","source":"CTD"},{"inference_gene_symbol":"SLC5A2","pathway_name":"Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds","react_pathway_id":"R-HSA-425366","source":"CTD"},{"inference_gene_symbol":"SLC5A2","pathway_name":"SLC-mediated transmembrane transport","react_pathway_id":"R-HSA-425407","source":"CTD"},{"inference_gene_symbol":"SLC5A2","pathway_name":"Na+-dependent glucose transporters","react_pathway_id":"R-HSA-428808","source":"CTD"},{"inference_gene_symbol":"SLC5A2","pathway_name":"Inositol transporters","react_pathway_id":"R-HSA-429593","source":"CTD"},{"inference_gene_symbol":"SLC5A2","pathway_name":"Metabolism of carbohydrates","react_pathway_id":"R-HSA-71387","source":"CTD"}]},"disease_ontology":{"_license":"https://github.com/DiseaseOntology/HumanDiseaseOntology/blob/master/DO_LICENSE.txt","ancestors":["DOID:0050736","DOID:557","DOID:9432","DOID:0050177","DOID:630","DOID:4","DOID:7","DOID:0050737","DOID:447","DOID:18","DOID:0050739"],"children":[],"def":"\"A renal glycosuria that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the SLC5A2 gene on chromosome 16p11.2.\" [url:https\\://pubmed.ncbi.nlm.nih.gov/19965550/, url:https\\://pubmed.ncbi.nlm.nih.gov/30942416/]","descendants":[],"doid":"DOID:0070613","name":"familial renal glucosuria","parents":["DOID:0050736","DOID:0050737","DOID:9432"],"synonyms":{"exact":["familial renal glycosuria","FRG","hereditary renal glycosuria","SGLT2 deficiency"]},"xrefs":{"gard":"7548","icd10":"E74.818","mesh":"D006030","mim":"233100","ordo":"69076","snomedct_us_2025_09_01":"226309007","umls_cui":"C3245525"}},"hpo":[{"clinical_modifier":{"biocuration":{"date":"2012-10-17","name":"HPO:skoehler"},"evidence":"TAS","hpo_id":"HP:0003828","hpo_name":"Variable expressivity","omim_refs":"OMIM:233100","original_disease_id":"OMIM:233100"},"disease_name":"Renal glucosuria","inheritance":[{"biocuration":{"date":"2009-02-17","name":"HPO:iea"},"evidence":"IEA","hpo_id":"HP:0000007","hpo_name":"Autosomal recessive inheritance","omim_refs":"OMIM:233100","original_disease_id":"OMIM:233100"},{"biocuration":{"date":"2012-10-17","name":"HPO:skoehler"},"evidence":"TAS","hpo_id":"HP:0000006","hpo_name":"Autosomal dominant inheritance","omim_refs":"OMIM:233100","original_disease_id":"OMIM:233100"}],"omim":"233100","phenotype_related_to_disease":[{"biocuration":{"date":"2009-02-17","name":"HPO:iea"},"evidence":"IEA","hpo_id":"HP:0001959","omim_refs":"OMIM:233100","original_disease_id":"OMIM:233100"},{"biocuration":{"date":"2009-02-17","name":"HPO:iea"},"evidence":"IEA","hpo_id":"HP:0002591","omim_refs":"OMIM:233100","original_disease_id":"OMIM:233100"},{"biocuration":{"date":"2009-02-17","name":"HPO:iea"},"evidence":"IEA","hpo_id":"HP:0003076","omim_refs":"OMIM:233100","original_disease_id":"OMIM:233100"},{"biocuration":{"date":"2009-02-17","name":"HPO:iea"},"evidence":"IEA","hpo_id":"HP:0000103","omim_refs":"OMIM:233100","original_disease_id":"OMIM:233100"},{"biocuration":{"date":"2010-06-18","name":"HPO:skoehler"},"evidence":"TAS","hp_freq":"HP:0040283","hpo_id":"HP:0010677","omim_refs":"OMIM:233100","original_disease_id":"OMIM:233100"}]},{"disease_name":"Familial renal glucosuria","orphanet":"69076","phenotype_related_to_disease":[{"biocuration":{"date":"2026-06-23","name":"ORPHA:orphadata"},"evidence":"TAS","hp_freq":"HP:0040280","hpo_id":"HP:0000112","orphanet_refs":"orphanet:69076"},{"biocuration":{"date":"2026-06-23","name":"ORPHA:orphadata"},"evidence":"TAS","hp_freq":"HP:0040280","hpo_id":"HP:0000124","orphanet_refs":"orphanet:69076"},{"biocuration":{"date":"2026-06-23","name":"ORPHA:orphadata"},"evidence":"TAS","hp_freq":"HP:0040280","hpo_id":"HP:0003076","orphanet_refs":"orphanet:69076"},{"biocuration":{"date":"2026-06-23","name":"ORPHA:orphadata"},"evidence":"TAS","hp_freq":"HP:0040283","hpo_id":"HP:0000010","orphanet_refs":"orphanet:69076"},{"biocuration":{"date":"2026-06-23","name":"ORPHA:orphadata"},"evidence":"TAS","hp_freq":"HP:0040283","hpo_id":"HP:0001944","orphanet_refs":"orphanet:69076"},{"biocuration":{"date":"2026-06-23","name":"ORPHA:orphadata"},"evidence":"TAS","hp_freq":"HP:0040283","hpo_id":"HP:0001946","orphanet_refs":"orphanet:69076"},{"biocuration":{"date":"2026-06-23","name":"ORPHA:orphadata"},"evidence":"TAS","hp_freq":"HP:0040283","hpo_id":"HP:0008855","orphanet_refs":"orphanet:69076"}]}],"mondo":{"ancestors":["MONDO:7770009","MONDO:0000001","MONDO:0037792","MONDO:0100191","MONDO:7770007","MONDO:0005240","MONDO:0019052","MONDO:7770008","MONDO:0019214","MONDO:0005066","MONDO:0045015","MONDO:7770006","MONDO:0019226","MONDO:0700096","MONDO:0006510","MONDO:0003847","MONDO:0017706","MONDO:0002118"],"definition":"Familial Renal Glucosuria (FRG) is characterized by the presence of persistent isolated glucosuria in the absence of both generalized proximal tubular dysfunction and hyperglycemia. FRG is usually considered a benign entity as most patients are not affected by severe clinical consequences. Polyuria and enuresis and later a mild growth and pubertal maturation delay are the only manifestations that have been reported during a follow-up period of 30 years. Episodic dehydration and ketosis during pregnancy and starvation and an increased incidence of urinary tract infections have occasionally been reported in severe cases. FRG is caused by loss-of-function mutations in the gene SLC5A2 (16p11.2). [Orphanet:69076]","disease_has_feature":{"hp":["HP:0003076"]},"excluded_subClassOf":{"mondo":["MONDO:0019743"]},"has_material_basis_in_germline_mutation_in":{"http":["http://identifiers.org/hgnc/11037"]},"label":"familial renal glucosuria","mondo":"MONDO:0009297","parents":["MONDO:0006510","MONDO:0019226","MONDO:0100191"],"synonym":{"exact":["familial renal glucosuria","Renal Glycosuria","SGLT2 deficiency"],"related":["GLYS","renal glucosuria","renal glycosuria"]},"xrefs":{"doid":["DOID:0070613","DOID:9432"],"gard":["0007548"],"icd11":["foundation:381783069"],"icd9":["271.4"],"meddra":["10038457"],"medgen":["757652"],"mesh":["D006030"],"nord":["1658"],"omim":["233100"],"orphanet":["69076"],"sctid":["267430007"],"umls":["C3245525"]}},"original_id":["orphanet:69076","UMLS:C0017980","UMLS:C3245525"],"umls":[{"_license":"https://www.nlm.nih.gov/research/umls/knowledge_sources/metathesaurus/release/license_agreement.html","icd9cm":{"preferred":"271.4"},"snomed":{"non-preferred":["190759004","367418000","236367002","154737003","267430007","1913007"],"preferred":["190759004","367418000","1913007","267430007","154737003"]},"umls":"C0017980"},{"_license":"https://www.nlm.nih.gov/research/umls/knowledge_sources/metathesaurus/release/license_agreement.html","icd10cm":{"non-preferred":"E74.818"},"mesh":{"non-preferred":"D006030"},"snomed":{"non-preferred":"226309007","preferred":["226309007","1913007"]},"umls":"C3245525"}]}