OntologiesdoidclassesDOID:0070259   
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congenital disorder of glycosylation type IIg
http://purl.obolibrary.org/obo/DOID_0070259

A congenital disorder of glycosylation type II that has_material_basis_in a mutation of the COG1 gene on chromosome 17q25.1.

Exact Synonyms
Carbohydrate deficient glycoprotein syndrome type IIg
CDG IIg
CDG2G
CDGII/COG1 cerebrocostomandibular-like syndrome
CDGIIg