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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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last database update
10/15/2019
MGI 6.14
The Jackson Laboratory