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Disease Ontology Browser
congenital disorder of glycosylation type I (DOID:0050570)
Alliance: disease page
Synonyms: ALG1-CDG; ALG2-CDG; ALG3-CDG; ALG6-CDG; ALG8-CDG; ALG9-CDG; ALG11-CDG; ALG12-CDG; DOLK-CDG; DPAGT1-CDG; DPM1-CDG; DPM2-CDG; DPM3-CDG; MPDU1-CDG; MPI-CDG; PMM2-CDG; RFT1-CDG; SRD5A3-CDG
Alt IDs: OMIM:212065, OMIM:300884, OMIM:300934, OMIM:601110, OMIM:602579, OMIM:603147, OMIM:607143, OMIM:607906, OMIM:608093, OMIM:608104, OMIM:608540, OMIM:608776, OMIM:608799, OMIM:609180, OMIM:610768, OMIM:612015, OMIM:612379, OMIM:612937, OMIM:613661, OMIM:614507, OMIM:614921, OMIM:615042, OMIM:615596, OMIM:615597, OMIM:616457
Definition: A congenital disorder of glycosylation involve disrupted synthesis of the lipid-linked oligosaccharide precursor.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
02/05/2019
MGI 6.13
The Jackson Laboratory