Disease #02046 (CDG2C;LAD2 (glycosylation, congenital disorder of, type IIc), OMIM:266265)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CDG2C;LAD2
Name	glycosylation, congenital disorder of, type IIc
OMIM ID	266265
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SLC35C1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2022-08-15 16:10:25 +02:00 (CEST)

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