Other Names for this Disease
- CDG 1B
- Carbohydrate-deficient glycoprotein syndrome type 1B
- MPI deficiency
- Protein-losing enteropathy-hepatic fibrosis syndrome
On this page
- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
- PubMed is a searchable database of medical literature and lists journal articles that discuss MPI-CDG (CDG-Ib). Click on the link to view a sample search on this topic.