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Summary Literature (0)
MIM:611182 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIh; CDG2H

Xenbase Genes: cog8

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012635 - COG8-congenital disorder of glycosylation

Disease Ontology (DO):
DOID:0050571 - congenital disorder of glycosylation type II
DOID:0070260 - congenital disorder of glycosylation type IIh