Erythrokeratodermia variabilis et progressiva 1

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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 1
MONDO_0017851
GJB3 Causal
10798362 9843209 10594760
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Erythrokeratodermia variabilis et progressiva 1.
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Peripheral neuropathy with sensorineural hearing impairment syndrome 1 shared geneGJB3 Related via 1 shared gene including GJB3. Erythrokeratoderma 1 shared geneGJB3 Related via 1 shared gene including GJB3. Deafness, autosomal recessive 1 shared geneGJB3 Related via 1 shared gene including GJB3. Deafness, digenic 1 shared geneGJB3 Related via 1 shared gene including GJB3. Greither disease 1 shared geneGJB3 Related via 1 shared gene including GJB3.