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DOID:0050570 - congenital disorder of glycosylation type I
Disease Ontology Definition:A congenital disorder of glycosylation characterized by under-glycosylated serum glycoproteins.
Synonyms: ALG1-CDG (CDG-1k), ALG11-CDG (CDG-1p), ALG12-CDG (CDG-1g), ALG2-CDG (CDG-1i), ALG3-CDG (CDG-1d), ALG6-CDG (CDG-1c), ALG8-CDG (CDG-1h), ALG9-CDG (CDG-1l), 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),
Xenbase Genes
:
alg2,
pgm1,
dpagt1,
dolk,
alg8,
ssr4,
stt3b,
mpi,
stt3a,
dpm3,
dpm1,
srd5a3,
alg3,
rtf1,
alg6,
| MONDO:0005500 - congenital disorder of glycosylation type I |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
congenital disorder of glycosylation (is_a)