Term Name:	glucose-galactose malabsorption
Synonyms:	GGM, monosaccharide malabsorption, SGLT1 deficiency
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.
Ontology:	Human Disease [DOID:0070563]   ( DOID:0070563 )