CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G

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Summary

Literature (0)

OMIM:607143 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G

Xenbase Genes: alg12

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011783 - ALG12-CDG

MONDO:0011783 - ALG12-CDG

Disease Ontology (DO):

DOID:0050570 - congenital disorder of glycosylation type I
DOID:0080559 - congenital disorder of glycosylation Ig

DOID:0050570 - congenital disorder of glycosylation type I

DOID:0080559 - congenital disorder of glycosylation Ig