Microvillus inclusion disease

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
MICROVILLUS INCLUSION DISEASE
2290C0341306MESH:C537470MONDO:0009635
MYO5B Unknown
18724368 19006234 20186687
CTD, Disgenet, GWAS catalog, Orphanet
STX3 Unknown
24726755
Disgenet, GenCC, Orphanet
STXBP2 Unknown — Disgenet, GenCC
All3 Causal0 Unknown3
Related Diseases Diseases that share the most curated genes with Microvillus inclusion disease.
5 View disease cluster →
Congenital microvillous atrophy 1 shared geneMYO5B Related via 1 shared gene including MYO5B. Congenital lactic acidosis 1 shared geneSTXBP2 Related via 1 shared gene including STXBP2. Hereditary hemophagocytic lymphohistiocytosis 1 shared geneSTXBP2 Related via 1 shared gene including STXBP2. Carotid artery thrombosis 1 shared geneSTXBP2 Related via 1 shared gene including STXBP2. Hemophagocytic lymphohistiocytosis 1 shared geneSTXBP2 Related via 1 shared gene including STXBP2.