Congenital reticular ichthyosiform erythroderma

Log in to bookmark this disease

Bookmark This Disease

Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CONGENITAL RETICULAR ICHTHYOSIFORM ERYTHRODERMA
281190MONDO:0012208C3665704
KRT1 Causal
25774499
GWAS catalog, Orphanet, Disgenet
KRT10 Causal
20798280
ClinVar, GenCC, Orphanet, Disgenet
All2 Causal2 Unknown0
Related Diseases Diseases that share the most curated genes with Congenital reticular ichthyosiform erythroderma.
5 View disease cluster →
Annular epidermolytic ichthyosis 2 shared genesKRT1, KRT10 Related via 2 shared genes including KRT1, KRT10. Epidermolytic ichthyosis 2 shared genesKRT1, KRT10 Related via 2 shared genes including KRT1, KRT10. Diffuse nonepidermolytic palmoplantar keratoderma 1 shared geneKRT1 Related via 1 shared gene including KRT1. Keratosis of greither 1 shared geneKRT1 Related via 1 shared gene including KRT1. Epidermolytic palmoplantar keratoderma 1 shared geneKRT1 Related via 1 shared gene including KRT1.