About   Help   FAQ
Disease Ontology Browser
congenital disorder of glycosylation type IIk (DOID:0070263)
Alliance: disease page
Synonyms: Carbohydrate deficient glycoprotein syndrome type IIk; CDG2K; CDG IIk; CDG syndrome type IIk; CDGIIdk; Congenital disorder of glycosylation type 2k; TMEM165-CDG
Alt IDs: OMIM:614727, ORDO:314667
Definition: A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of the TMEM165 gene on chromosome 4q12.

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
MGI 6.13
The Jackson Laboratory