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Disease Ontology Browser
congenital disorder of glycosylation type IIe (DOID:0070257)
Alliance: disease page
Synonyms: Carbohydrate deficient glycoprotein syndrome type IIe; CDG2E; CDG IIe; CDG syndrome type IIe; CDGIIde; COG7-CDG
Alt IDs: OMIM:608779, ORDO:79333, UMLS_CUI:C2931010
Definition: A congenital disorder of glycosylation type II that has_material_basis_in a mutation of COG7 on chromosome 16p12.2.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
02/11/2020
MGI 6.14
The Jackson Laboratory