Disease #03078

Official abbreviation CDG-1N
Name glycosylation, congenital disorder of, type In (CDG-1N)
OMIM ID 612015
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene RFT1
Associated tissues -
Disease features -
Remarks -