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Echinobase
Summary Literature (0)
MIM:212065 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A

Echinobase Genes:

Human Disease Resource: MIM


Disease Ontology (DO):
DOID:0050570 - congenital disorder of glycosylation type I
DOID:0080552 - congenital disorder of glycosylation Ia