Disease #02720 (CDG1I (glycosylation, congenital disorder of, type Ii (CDG-1I)), OMIM:607906)

Official abbreviation CDG1I
Name glycosylation, congenital disorder of, type Ii (CDG-1I)
OMIM ID 607906
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 ALG2
Associated tissues -
Disease features -
Remarks -