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Summary Literature (0)
MIM:616829 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIp; CDG2P

Xenbase Genes: tmem199

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014790 - TMEM199-CDG

Disease Ontology (DO):
DOID:0070268 - congenital disorder of glycosylation type IIp