Disease #05919 (CDG2N (glycosylation, congenital disorder of, type IIn (CDG2N)), OMIM:616721)

Global Variome shared LOVD

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Official abbreviation	CDG2N
Name	glycosylation, congenital disorder of, type IIn (CDG2N)
OMIM ID	616721
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SLC39A8
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-04-08 10:29:27 +02:00 (CEST)
Date last edited	N/A

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