Term Name: congenital disorder of glycosylation type IIg
Synonyms: Carbohydrate deficient glycoprotein syndrome type IIg, CDG IIg, CDG2G, CDGII/COG1 cerebrocostomandibular-like syndrome, CDGIIg
Definition: A congenital disorder of glycosylation type II that has_material_basis_in a mutation of the COG1 gene on chromosome 17q25.1.
Ontology: Human Disease [DOID:0070259]   ( DOID:0070259 )

Relationships
is a type of: autosomal recessive disease congenital disorder of glycosylation type II