Disease #04022

Official abbreviation CDG-1W
Name glycosylation, congenital disorder of, type Iw (CDG-1W)
OMIM ID 615596
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene STT3A
Associated tissues -
Disease features -
Remarks -