Search Ontology:
Human Disease

congenital disorder of glycosylation type IIg

Term ID
DOID:0070259
Synonyms
  • Carbohydrate deficient glycoprotein syndrome type IIg
  • CDG IIg
  • CDG2G
  • CDGII/COG1 cerebrocostomandibular-like syndrome
  • CDGIIg
Definition
A congenital disorder of glycosylation type II that has_material_basis_in a mutation of the COG1 gene on chromosome 17q25.1. https://www.ncbi.nlm.nih.gov/pubmed/16537452
References
Ontology
Human Disease   ( DOID:0070259 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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