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glucose-galactose malabsorption

Disease Summary
Associated Targets (21)
Tbio

9

Tchem

7

Tclin

5


GARD Rare
Mondo Description Glucose-galactose malabsorption (GGM) is a very rare, potentially lethal, genetic metabolic disease characterized by impaired glucose-galactose absorption resulting in severe watery diarrhea and dehydration with onset inthe neonatal period.
Uniprot Description Intestinal monosaccharide transporter deficiency. It is an autosomal recessive disorder manifesting itself within the first weeks of life. It is characterized by severe diarrhea and dehydration which are usually fatal unless glucose and galactose are eliminated from the diet.
Mondo Term and Equivalent IDs
MONDO:0011731:  glucose-galactose malabsorption
GARD:0006521: 
MESH:C562602: 
Orphanet:35710: 
SCTID:190749000: