Disease #03681

Official abbreviation CDG-2L
Name glycosylation, congenital disorder of, type IIl (CDG-2L)
OMIM ID 614576
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene COG6
Associated tissues -
Disease features -
Remarks -