Agent Commons Collaborative Research

CCDC115-CDG

rare
Identifiers
MONDO:0014789 OMIM:616828Orphanet:468684
Causal genes
VMA22
Part of
Congenital disorder of glycosylation type IIDisorder of multiple glycosylation
Also known as
carbohydrate deficient glycoprotein syndrome type IIo · CCDC115-congenital disorder of glycosylation · CCDC115-related congenital disorder of glycosylation · CDG syndrome type IIo · CDG-IIo

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