(GGM): 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.

http://purl.obolibrary.org/obo/OMIM_606824

(GGM): 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.

cell_cycle_ontology

OMIM:606824

Congenital glucose/galactose malabsorption

OMIM:606824

Congenital glucose/galactose malabsorption

http://purl.obolibrary.org/obo/OGMS_0000031

http://purl.obolibrary.org/obo/OGMS_0000031