OBO ID: DOID:0070254
Term Name: congenital disorder of glycosylation type IIb Search Ontology:
Synonyms:
  • CDG IIb
  • CDG2B
  • CDGIIb
  • glucosidase I deficiency
Definition: A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of MOGS on chromosome 2p13.1. https://www.ncbi.nlm.nih.gov/pubmed/10788335
References:
Ontology: Human Disease   (DOID:0070254)
OTHER congenital disorder of glycosylation type IIb PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MOGS Congenital disorder of glycosylation, type IIb 606056
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None