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DO Term : familial renal glucosuria [DOID:0070613] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A renal glycosuria that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the SLC5A2 gene on chromosome 16p11.2.
  • synonyms:
  • GARD:7548,
  • SGLT2 deficiency,
  • FRG,
  • SNOMEDCT_US_2023_03_01:226309007,
  • UMLS_CUI:C3245525,
  • 233100,
  • MESH:D006030,
  • familial renal glycosuria,
  • OMIM:233100,
  • hereditary renal glycosuria,
  • ORDO:69076
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Disease

Diseases --> Human genes

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Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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