Disease #02635 (CDG-1G (glycosylation, congenital disorder of, type Ig (CDG-1G)), OMIM:607143)

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Official abbreviation	CDG-1G
Name	glycosylation, congenital disorder of, type Ig (CDG-1G)
OMIM ID	607143
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ALG12
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A