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Disease Ontology Browser
congenital disorder of glycosylation type I (DOID:0050570)
Synonyms: ALG1-CDG (CDG-1k); ALG2-CDG (CDG-1i); ALG3-CDG (CDG-1d); ALG6-CDG (CDG-1c); ALG8-CDG (CDG-1h); ALG9-CDG (CDG-1l); ALG11-CDG (CDG-1p); ALG12-CDG (CDG-1g); DOLK-CDG (CDG-1m); DPAGT1-CDG (CDG-1j); DPM1-CDG (CDG-1e); DPM2-CDG (CDG-1u); DPM3-CDG (CDG-1o); MPDU1-CDG (CDG-1f); MPI-CDG (CDG-1b); PMM2-CDG (CDG-1a); RFT1-CDG (CDG-1n); SRD5A3-CDG (CDG-1q)
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
04/18/2017
MGI 6.08
The Jackson Laboratory