Preferred Label : COG8 protein, human;
MeSH note : COG - conserved oligomeric Golgi; deficiency causes congenital disorder of glycosylation
type IIh; RefSeq NM_032382;
MeSH synonym : component of oligomeric golgi complex 8 protein, human;
Is substance : O;
Origin ID : C522290;
UMLS CUI : C2000250;
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