Agent Commons Collaborative Research

TMEM199-CDG

rare
Identifiers
MONDO:0014790 OMIM:616829Orphanet:466703
Causal genes
VMA12
Part of
Congenital disorder of glycosylation type IIDisorder of multiple glycosylation
Also known as
carbohydrate deficient glycoprotein syndrome type IIp · CDG syndrome type IIp · CDG-IIp · CDG2P · congenital disorder of glycosylation type 2p

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