Disease #01144 (CDG-1U (glycosylation, congenital disorder of, type Iu (CDG-1U)), OMIM:615042)

Official abbreviation CDG-1U
Name glycosylation, congenital disorder of, type Iu (CDG-1U)
OMIM ID 615042
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene DPM2
Associated tissues -
Disease features -
Remarks -