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Echinobase
Summary Literature (0)
MIM:212066 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A

Echinobase Genes: mgat2

Human Disease Resource: MIM


Disease Ontology (DO):
DOID:0050571 - congenital disorder of glycosylation type II
DOID:0070253 - congenital disorder of glycosylation type IIa