Search Ontology:
Human Disease

congenital disorder of glycosylation type IIi

Term ID
DOID:0070261
Synonyms
  • Carbohydrate deficient glycoprotein syndrome type IIi
  • CDG IIi
  • CDG syndrome type IIi
  • CDG2I
  • CDGIIi
  • COG5-CDG
  • Congenital disorder of glycosylation type 2i
Definition
A congenital disorder of glycosylation type II that has_material_basis_in a mutation of the COG5 gene on chromosome 7q22.3. https://www.ncbi.nlm.nih.gov/pubmed/19690088
References
Ontology
Human Disease   ( DOID:0070261 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models