Disease #05241 (CDG2O (glycosylation, congenital disorder of, type IIo (CDG-2O)), OMIM:616828)

Global Variome shared LOVD

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Official abbreviation	CDG2O
Name	glycosylation, congenital disorder of, type IIo (CDG-2O)
OMIM ID	616828
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CCDC115
Associated tissues	-
Disease features	-
Remarks	-
Date created	2017-03-19 17:30:54 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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