Riboflavin deficiency

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
RIBOFLAVIN DEFICIENCY
615026C0035528MESH:D012257
SLC52A1 Unknown
21089064
CTD, Disgenet, HPO
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Riboflavin deficiency.
5 View disease cluster →
maternal riboflavin deficiency 1 shared geneSLC52A1 Related via 1 shared gene including SLC52A1. Riboflavin transporter deficiency 1 shared geneSLC52A1 Related via 1 shared gene including SLC52A1. Ovarian epithelial cancer 1 shared geneSLC52A1 Related via 1 shared gene including SLC52A1. Peptic ulcer disease 1 shared geneSLC52A1 Related via 1 shared gene including SLC52A1. Ovarian cancer 1 shared geneSLC52A1 Related via 1 shared gene including SLC52A1.