Disease #02980

Official abbreviation CDG-1M
Name glycosylation, congenital disorder of, type Im (CDG-1M)
OMIM ID 610768
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene DOLK
Associated tissues -
Disease features -
Remarks -