Disease #03383 (CDG-1P (glycosylation, congenital disorder of, type IP (CDG-1P)), OMIM:613661)

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	Curator: Johan T. den Dunnen

Official abbreviation	CDG-1P
Name	glycosylation, congenital disorder of, type IP (CDG-1P)
OMIM ID	613661
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ALG11
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A