Hereditary folate malabsorption

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
FOLATE MALABSORPTION, HEREDITARY
C0342705229050MESH:C562799
SARM1 Unknown — Disgenet
SLC46A1 Unknown
21346251
CTD, Disgenet, HPO, ClinGen
All2 Causal0 Unknown2
Related Diseases Diseases that share the most curated genes with Hereditary folate malabsorption.
5 View disease cluster →
Congenital folate absorption defect 1 shared geneSLC46A1 Related via 1 shared gene including SLC46A1. Malabsorption syndrome 1 shared geneSLC46A1 Related via 1 shared gene including SLC46A1. Hyperhomocysteinemia 1 shared geneSLC46A1 Related via 1 shared gene including SLC46A1. Pancytopenia 1 shared geneSLC46A1 Related via 1 shared gene including SLC46A1. Visual disorder 1 shared geneSARM1 Related via 1 shared gene including SARM1.