Regulation of Transcription Ontology

Last uploaded: December 4, 2018
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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