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Disease Ontology Browser
glucose-galactose malabsorption (DOID:0070563)
Alliance: disease page
Synonyms: GGM; monosaccharide malabsorption; SGLT1 deficiency
Alt IDs: OMIM:606824, MESH:C562602, ORDO:35710, UMLS_CUI:C0268186
Definition: A glucose metabolism disease characterized by a defect in glucose and galactose transport across the intestinal brush border, resulting in neonatal onset of life-threatening watery diarrhea and dehydration, that has_material_basis_in homozygous mutation in the SLC5A1 gene on chromosome 22q12.3.

Contributing Projects:
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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Send questions and comments to User Support. 		last database update
08/21/2024
MGI 6.24 		The Jackson Laboratory