Disease #02793 (CDG1E (glycosylation, congenital disorder of, type Ie (CDG-1E)), OMIM:608799)

Official abbreviation CDG1E
Name glycosylation, congenital disorder of, type Ie (CDG-1E)
OMIM ID 608799
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene DPM1
Associated tissues -
Disease features -
Remarks -