Cell Cycle Ontology

Last uploaded: June 26, 2014
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Preferred Name

Congenital glucose/galactose malabsorption
Synonyms
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://purl.obolibrary.org/obo/OMIM_606824
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.
has_obo_namespace

cell_cycle_ontology
id

OMIM:606824
label

Congenital glucose/galactose malabsorption
notation

OMIM:606824
prefLabel

Congenital glucose/galactose malabsorption
treeView

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

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