Disease #04023

Official abbreviation CDG-1X
Name glycosylation, congenital disorder of, type Ix (CDG-1X)
OMIM ID 615597
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene STT3B
Associated tissues -
Disease features -
Remarks -