Disease #02197

Official abbreviation CDG-1S
Name glycosylation, congenital disorder of, type Is (CDG-1S)
OMIM ID 300884
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene ALG13
Associated tissues -
Disease features -
Remarks -