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Disease Ontology Browser
congenital disorder of glycosylation type IId (DOID:0070256)
Alliance: disease page
Synonyms: CDG2D; CDG IId; CDGIId
Alt IDs: OMIM:607091, MESH:C535753, ORDO:79332, UMLS_CUI:C2931009
Definition: A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of the B4GALT1 gene on chromosome 9p21.1.

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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Send questions and comments to User Support. 		last database update
04/16/2024
MGI 6.23 		The Jackson Laboratory