Dentin dysplasia

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
DENTIN DYSPLASIA TYPE I
MONDO:0007436
SMOC2 Causal
22152679 23317772
ClinVar, GenCC —
All17 Causal1 Unknown17
Related Diseases Diseases that share the most curated genes with Dentin dysplasia.
5 View disease cluster →
Dentinogenesis imperfecta 14 shared genesSLC24A4, AMBN, AMELX, DLX3, ENAM, FAM20A, FAM83H, ITGB6, KLK4, LAMB3, MMP20, ODAPH +2 more Related via 14 shared genes including SLC24A4, AMBN, AMELX. Amelogenesis imperfecta 13 shared genesSLC24A4, AMBN, AMELX, DLX3, ENAM, FAM20A, FAM83H, ITGB6, KLK4, LAMB3, MMP20, ODAPH +1 more Related via 13 shared genes including SLC24A4, AMBN, AMELX. Hypomaturation amelogenesis imperfecta 6 shared genesSLC24A4, AMELX, KLK4, MMP20, ODAPH, WDR72 Related via 6 shared genes including SLC24A4, AMELX, KLK4. Tricho-dento-osseous syndrome 1 shared geneDLX3 Related via 1 shared gene including DLX3. Enamel-renal syndrome 1 shared geneFAM20A Related via 1 shared gene including FAM20A.