Epidermolytic hyperkeratosis 2b, autosomal recessive

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Subtype of: Epidermolytic ichthyosis
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Epidermolytic hyperkeratosis 2B, autosomal recessive
MONDO_0700245
KRT10 Causal
16505000 20302579 18219278 19474805
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Epidermolytic hyperkeratosis 2b, autosomal recessive.
5 View disease cluster →
Ichthyosis with confetti 1 shared geneKRT10 Related via 1 shared gene including KRT10. Ichthyosis histrix, lambert type 1 shared geneKRT10 Related via 1 shared gene including KRT10. Epidermolytic hyperkeratosis 2a 1 shared geneKRT10 Related via 1 shared gene including KRT10. Annular epidermolytic ichthyosis 1 shared geneKRT10 Related via 1 shared gene including KRT10. Epidermolytic ichthyosis 1 shared geneKRT10 Related via 1 shared gene including KRT10.