Link to this page
Regulation of Transcription Ontology
Last uploaded:
December 4, 2018
Jump to:
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 |
Add comment
Delete | Subject | Author | Type | Created |
---|---|---|---|---|
No notes to display |
Create mapping
Mapping To | Ontology | Source |
---|---|---|
http://identifiers.org/omim/606824 | REXO | SAME_URI |
http://identifiers.org/omim/606824 | GEXO | SAME_URI |
http://identifiers.org/omim/606824 | REXO | LOOM |
http://identifiers.org/omim/606824 | GEXO | 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 |