Disease #02790 (CDG-1L (glycosylation, congenital disorder of, type Il (CDG-1L)), OMIM:608776)

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Official abbreviation	CDG-1L
Name	glycosylation, congenital disorder of, type Il (CDG-1L)
OMIM ID	608776
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ALG9
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A