Diarrhea 12, 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 12, with microvillus atrophy
MONDO_0030335
STX3 Causal
29282386 29266534 25358429 24726755 33974130
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Diarrhea 12, with microvillus atrophy.
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Microvillus inclusion disease 1 shared geneSTX3 Related via 1 shared gene including STX3. Color vision deficiency 1 shared geneSTX3 Related via 1 shared gene including STX3.