Disease #04022 (CDG1W (glycosylation, congenital disorder of, type Iw (CDG1W)), OMIM:615596)

Official abbreviation	CDG1W
Name	glycosylation, congenital disorder of, type Iw (CDG1W)
OMIM ID	615596
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant, Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	STT3A
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-10-14 19:09:07 +02:00 (CEST)

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Global Variome shared LOVD