Mowat-wilson syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
MOWAT-WILSON SYNDROME
235730C1856113MESH:C536990MONDO:0009341
ZEB2 Causal
15006694 17103451 17478475 16532472 9719364 11891681 11279515 16688751 12920073 12451214 11592033 16088920 11595972
CTD, ClinGen, ClinVar, Disgenet, GWAS catalog, HPO
MOWAT-WILSON SYNDROME DUE TO A ZEB2 POINT MUTATION
261552C5679681
ZEB2 Unknown
20301585
Disgenet, Orphanet
MOWAT-WILSON SYNDROME DUE TO MONOSOMY 2Q22
261537C5437617
ZEB2 Unknown
20301585 11279515 11592033 11595972 11891681 12451214 12920073 16088920 16532472 16688751 9719364
Orphanet, Disgenet, ClinGen
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Mowat-wilson syndrome.
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Cerebellar diseases 1 shared geneZEB2 Related via 1 shared gene including ZEB2. Lennox-gastaut syndrome 1 shared geneZEB2 Related via 1 shared gene including ZEB2. Papillary thyroid cancer 1 shared geneZEB2 Related via 1 shared gene including ZEB2. Pena-shokeir syndrome 1 shared geneZEB2 Related via 1 shared gene including ZEB2. Hirschsprung disease 1 shared geneZEB2 Related via 1 shared gene including ZEB2.