Gene Expression Ontology

Last uploaded: December 16, 2015

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

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://identifiers.org/omim/606824	REXO	SAME_URI
http://identifiers.org/omim/606824	RETO	SAME_URI
http://identifiers.org/omim/606824	REXO	LOOM
http://identifiers.org/omim/606824	RETO	LOOM
http://purl.obolibrary.org/obo/OMIM_606824	CCO	LOOM
http://purl.jp/bio/4/id/200906087043968860	IOBC	LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/27943000	SNOMEDCT	LOOM
http://purl.bioontology.org/ontology/SNMI/D6-54320	SNMI	LOOM