Your browser does not support javascript:   Search for gard hereSearch for news-and-events here.


Genetic and Rare Diseases Information Center (GARD)

Print friendly version

Congenital disorder of glycosylation type 1B

See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.

Other Names for Congenital disorder of glycosylation type 1B

  • Carbohydrate-deficient glycoprotein syndrome type 1B
  • CDG 1B
  • CDG gastrointestinal type
  • CDG1B
  • Mannosephosphate isomerase deficiency
  • MPI deficiency
  • Protein-losing enteropathy-hepatic fibrosis syndrome
  • Saguenay Lac Saint Jean syndrome
  • SLSJ syndrome