Dyschromatosis symmetrica hereditaria

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 1
127500C2675711MESH:C567273MONDO:0024524
SASH1 Causal — CTD, ClinVar, Disgenet, GenCC, HPO —
DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 3
615402C3809394MONDO:0014169OMIM:615402
ABCB6 Causal
24224009 23519333 29940187 25288164 24498303
CTD, ClinGen, ClinVar, Disgenet, HPO
All3 Causal2 Unknown3
Related Diseases Diseases that share the most curated genes with Dyschromatosis symmetrica hereditaria.
5 View disease cluster →
Cancer, alopecia, pigment dyscrasia, onychodystrophy, and keratoderma 1 shared geneSASH1 Related via 1 shared gene including SASH1. Dyschromatosis 1 shared geneSASH1 Related via 1 shared gene including SASH1. microphthalmia, isolated, with coloboma 7 1 shared geneABCB6 Related via 1 shared gene including ABCB6. Cleft eyelid 1 shared geneABCB6 Related via 1 shared gene including ABCB6. Congenital iris coloboma 1 shared geneABCB6 Related via 1 shared gene including ABCB6.