Other Names for this Disease
- CDG 1H
- ALG8-CDG (CDG-Ih)
- Congenital disorder of glycosylation, type Ih
- CDG syndrome type Ih
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 ALG8-CDG (CDG-Ih). Click on the link to view a sample search on this topic.