Regulation of Gene Expression Ontolology

Last uploaded: December 16, 2015
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Preferred Name

Congenital glucose|galactose malabsorption
Synonyms

GGM
Definitions

(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.
ID

http://identifiers.org/omim/606824
altLabel

GGM
definition

(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.
id

OMIM:606824
notation

OMIM:606824
prefLabel

Congenital glucose|galactose malabsorption
subClassOf

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