Congenital disorder of glycosylation type 2A
Other Names for this Disease
- Carbohydrate-deficient glycoprotein syndrome type 2
- CDG 2A
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- 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.
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