congenital disorder of glycosylation, type iit

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
congenital disorder of glycosylation, type iit
GALNT2 Causal
32293671 27508872
ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with congenital disorder of glycosylation, type iit.
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Lipoprotein lipase deficiency 1 shared geneGALNT2 Related via 1 shared gene including GALNT2. Fatty liver 1 shared geneGALNT2 Related via 1 shared gene including GALNT2. Congenital disorder of glycosylation 1 shared geneGALNT2 Related via 1 shared gene including GALNT2. Atherosclerosis 1 shared geneGALNT2 Related via 1 shared gene including GALNT2. Hyperlipidemia 1 shared geneGALNT2 Related via 1 shared gene including GALNT2.