(Q55784972)
English
SLC39A8-CDG
human disease
- congenital disorder of glycosylation type IIn
- SLC39A8 deficiency
- Carbohydrate deficient glycoprotein syndrome type IIn
- Congenital Disorder of Glycosylation, Type Iin
- CDG IIn
- CDG2N
- Congenital disorder of glycosylation type IIn
- CDG-IIn
- CDGIIdn
- CDG syndrome type IIn
- Congenital disorder of glycosylation type 2n
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