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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)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory