Diarrhea 2, with microvillus atrophy

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Subtype of: Atrophy
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Diarrhea 2, with microvillus atrophy
MONDO_0009635
MYO5B Unknown
18724368 19006234 20186687 21206382 24014347 24138727 24892806 28027573 29266534 32304554 33525641 34816459
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Diarrhea 2, with microvillus atrophy.
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Congenital microvillous atrophy 1 shared geneMYO5B Related via 1 shared gene including MYO5B. Microvillus inclusion disease 1 shared geneMYO5B Related via 1 shared gene including MYO5B. Progressive intrahepatic cholestasis 1 shared geneMYO5B Related via 1 shared gene including MYO5B. Intestinal disease 1 shared geneMYO5B Related via 1 shared gene including MYO5B. Amphetamine or sympathomimetic abuse 1 shared geneMYO5B Related via 1 shared gene including MYO5B.