Malabsorption syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
MALABSORPTION SYNDROME
C0024523
SLC46A1 Unknown — Disgenet
MALABSORPTION SYNDROMES
MESH:D008286
SLC46A1 Unknown
17129779 17446347
CTD
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Malabsorption syndrome.
5 View disease cluster →
Congenital folate absorption defect 1 shared geneSLC46A1 Related via 1 shared gene including SLC46A1. Hereditary folate malabsorption 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. Anemia 1 shared geneSLC46A1 Related via 1 shared gene including SLC46A1.