Bile acid malabsorption

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
BILE ACID MALABSORPTION, PRIMARY
MESH:C567652
SLC10A2 Unknown — CTD
BILE ACID MALABSORPTION, PRIMARY, 1
613291C5561934MONDO:0013214
SLC10A2 Unknown
9109432
ClinVar, Disgenet, GWAS catalog, HPO
BILE ACID MALABSORPTION, PRIMARY, 2
619481C5561962MONDO:0859180
SLC51B Causal
28898457
ClinVar, Disgenet, HPO
RASL12 Unknown — Disgenet —
All3 Causal1 Unknown2
Related Diseases Diseases that share the most curated genes with Bile acid malabsorption.
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Diabetes complications 2 shared genesSLC10A2, SLC51B Related via 2 shared genes including SLC10A2, SLC51B. Intestinal disease 1 shared geneSLC10A2 Related via 1 shared gene including SLC10A2. Cognition disorder 2 shared genesSLC10A2, SLC51B Related via 2 shared genes including SLC10A2, SLC51B. Delirium, dementia, and cognitive disorders 2 shared genesSLC10A2, SLC51B Related via 2 shared genes including SLC10A2, SLC51B. Cholelithiasis 2 shared genesRASL12, SLC51B Related via 2 shared genes including RASL12, SLC51B.