(Q18553314)
English
congenital disorder of glycosylation type II
congenital disorder of glycosylation that involves malfunctioning trimming/processing of the protein-bound oligosaccharide chain
- B4GALT1-CDG (CDG-2d)
- MGAT2-CDG (CDG-2a)
- MOGS-CDG (CDG-2b)
- MOGS-CDG
- B4GALT1-CDG
- MGAT2-CDG
- Congenital disorder of glycosylation type 2a
- CDG2A
- Carbohydrate-Deficient Glycoprotein Syndrome, Type Ii
- Carbohydrate deficient glycoprotein syndrome type IIa
- Mental Retardation, Growth Retardation, Prominent Columella, and Open Mouth
- CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A
- CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa
- N-acetylglucosaminyltransferase 2 deficiency
- CDG-IIa
- Alkuraya Syndrome
- Cdg Iia
- CDG syndrome type IIa
- Congenital disorder of glycosylation type IIa
- Carbohydrate-Deficient Glycoprotein Syndrome, Type Ii, Formerly
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