congenital disorder of glycosylation type i Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A congenital disorder of glycosylation involve disrupted synthesis of the lipid-linked oligosaccharide precursor. (Human Disease Ontology, DOID_0050570)
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Genes

6 genes co-occuring with the disease congenital disorder of glycosylation type i in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
PMM2 phosphomannomutase 2 1.19489
TF transferrin 1.10931
SERPINA1 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 1 0.789262
CP ceruloplasmin (ferroxidase) 0.569552
HP haptoglobin 0.559062
HPR haptoglobin-related protein 0.552463