Search Ontology:
Human Disease

congenital disorder of glycosylation type II

Term ID
DOID:0050571
Synonyms
Definition
A congenital disorder of glycosylation that involves malfunctioning trimming or processing of the protein-bound oligosaccharide chain. http://en.wikipedia.org/wiki/Congenital_disorder_of_glycosylation#Classification
References
Ontology
Human Disease   ( DOID:0050571 )
Relationships
is a type of
has subtype
Other Pages
Genes Involved
Zebrafish Models