Erythrokeratodermia variabilis et progressiva 7

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Subtype of: Erythrokeratodermia variabilis
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Erythrokeratodermia variabilis et progressiva 7
MONDO_0030941
PERP Causal
30321533 31898316
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Erythrokeratodermia variabilis et progressiva 7.
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Congenital palmoplantar and perioral keratoderma of olmsted 1 shared genePERP Related via 1 shared gene including PERP. Greither disease 1 shared genePERP Related via 1 shared gene including PERP. Olmsted syndrome 1 shared genePERP Related via 1 shared gene including PERP. Erythrokeratodermia variabilis 1 shared genePERP Related via 1 shared gene including PERP. Bulimia 1 shared genePERP Related via 1 shared gene including PERP.