congenital disorder of glycosylation type I
Go to external page http://purl.obolibrary.org/obo/MONDO_0005500
A congenital disorder of glycosylation involve disrupted synthesis of the lipid-linked oligosaccharide precursor. [ http://en.wikipedia.org/wiki/Congenital_disorder_of_glycosylation#Classification DOID:0050570 ]
Synonyms: congenital disorders of glycosylation, type I
Term information
- EFO:0005545 (MONDO:equivalentTo)
- DOID:0050570 (MONDO:equivalentTo)
- OMIMPS:212065 (MONDO:equivalentTo)
rare, inferred_rare
DPM3-CDG
PMM2-CDG (CDG-1a)
DOLK-CDG
DPM2-CDG (CDG-1u)
MPDU1-CDG (CDG-1f)
DPAGT1-CDG
ALG12-CDG (CDG-1g)
ALG6-CDG (CDG-1c)
DPM1-CDG (CDG-1e)
ALG6-CDG
ALG9-CDG
ALG12-CDG
DPAGT1-CDG (CDG-1j)
MPI-CDG (CDG-1b)
ALG3-CDG (CDG-1d)
ALG1-CDG
MPDU1-CDG
DPM3-CDG (CDG-1o)
SRD5A3-CDG
PMM2-CDG
ALG3-CDG
MPI-CDG
SRD5A3-CDG (CDG-1q)
DPM1-CDG
ALG2-CDG
ALG11-CDG
ALG8-CDG
ALG11-CDG (CDG-1p)
DOLK-CDG (CDG-1m)
ALG1-CDG (CDG-1k)
ALG2-CDG (CDG-1i)
DPM2-CDG
RFT1-CDG
ALG8-CDG (CDG-1h)
RFT1-CDG (CDG-1n)
ALG9-CDG (CDG-1l)