Disease #02341 (CDG-1D (glycosylation, congenital disorder of, type Id (CDG-1D)), OMIM:601110)

MyGenome LOVD - This database is for training purposes only

LOVD v.3.0 Build 30 [ Current LOVD status ]
Log in

	Curator: Johan T. den Dunnen

Official abbreviation	CDG-1D
Name	glycosylation, congenital disorder of, type Id (CDG-1D)
OMIM ID	601110
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ALG3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A