Disease #01690 (CDG-2A (glycosylation, congenital disorder of, type IIa (CDG-2A)), OMIM:212066)

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	Curator: Johan T. den Dunnen

Official abbreviation	CDG-2A
Name	glycosylation, congenital disorder of, type IIa (CDG-2A)
OMIM ID	212066
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MGAT2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A