About   Help   FAQ
Disease Ontology Browser
congenital disorder of glycosylation type I (DOID:0050570)
Alliance: disease page
Alt IDs: OMIM:PS212065
Definition: A congenital disorder of glycosylation characterized by under-glycosylated serum glycoproteins.

Disease References using Mouse Models (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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/05/2024
MGI 6.24 		The Jackson Laboratory