Congenital disorder of glycosylation with defective fucosylation 2

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Subtype of: Congenital disorder of glycosylation
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Congenital disorder of glycosylation with defective fucosylation 2
MONDO_0060720
FCSK Causal
30503518
ClinGen, Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Congenital disorder of glycosylation with defective fucosylation 2.
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Congenital disorder of glycosylation 1 shared geneFCSK Related via 1 shared gene including FCSK. Neurodevelopmental disorder 1 shared geneFCSK Related via 1 shared gene including FCSK. Obesity 1 shared geneFCSK Related via 1 shared gene including FCSK.