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Summary Literature (0)
MIM:607091 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IId; CDG2D

Xenbase Genes: b4galt1.2, b4galt1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011772 - lower jaw opening

Disease Ontology (DO):
DOID:0050571 - congenital disorder of glycosylation type II
DOID:0070256 - congenital disorder of glycosylation type IId