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Disease Ontology Browser
congenital disorder of glycosylation type IIl (DOID:0070264)
Alliance: disease page
Synonyms: CDG2L; CDG IIl; CDG syndrome type IIL; CDGIIdl; COG6-CGD; Congenital disorder of glycosylation type 2l
Alt IDs: OMIM:614576, ORDO:464443
Definition: A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of COG6 on chromosome 13q14.11.


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