Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026
Id http://purl.bioontology.org/ontology/OMIM/619525
http://purl.bioontology.org/ontology/OMIM/619525
Preferred Name

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIw
Synonyms
CDG2W
Type http://www.w3.org/2002/07/owl#Class

All Properties

altLabel
CDG2W
prefLabel
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIw
Gene Symbol
CDG2W
G6PT1
SLC37A4
Scope Statement
Caused by mutation solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene (SLC37A4, 602671.0017) [MOLECULAR BASIS]
type
Has manifestation
http://purl.bioontology.org/ontology/OMIM/MTHU057216
http://purl.bioontology.org/ontology/OMIM/MTHU048518
http://purl.bioontology.org/ontology/OMIM/MTHU000263
http://purl.bioontology.org/ontology/OMIM/MTHU000576
http://purl.bioontology.org/ontology/OMIM/MTHU042548
http://purl.bioontology.org/ontology/OMIM/MTHU000212
http://purl.bioontology.org/ontology/OMIM/MTHU002522
http://purl.bioontology.org/ontology/OMIM/MTHU001106
http://purl.bioontology.org/ontology/OMIM/MTHU036798
http://purl.bioontology.org/ontology/OMIM/MTHU005530
http://purl.bioontology.org/ontology/OMIM/MTHU000389
http://purl.bioontology.org/ontology/OMIM/MTHU037221
http://purl.bioontology.org/ontology/OMIM/MTHU000036
http://purl.bioontology.org/ontology/OMIM/MTHU008649
http://purl.bioontology.org/ontology/OMIM/MTHU036338
http://purl.bioontology.org/ontology/OMIM/MTHU000081
http://purl.bioontology.org/ontology/OMIM/MTHU011727
http://purl.bioontology.org/ontology/OMIM/MTHU011439
http://purl.bioontology.org/ontology/OMIM/MTHU074250
http://purl.bioontology.org/ontology/OMIM/MTHU002606
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tui
T047
Gene Locus
11q23
MIMTYPEMEANING
Phenotype description, molecular basis known.
notation
619525
Semantic type UMLS property
Has inheritance type
cui
C5561986
OMIM Entry Type
3
OMIM MimType Value
pound
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