Nephropathy with pretibial epidermolysis bullosa and deafness

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
NEPHROPATHY WITH PRETIBIAL EPIDERMOLYSIS BULLOSA AND DEAFNESS
C1836823MESH:C563798
CD151 Unknown
15265795
CTD, Disgenet
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Nephropathy with pretibial epidermolysis bullosa and deafness.
3 View disease cluster →
Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome 1 shared geneCD151 Related via 1 shared gene including CD151. Nephrotic syndrome-epidermolysis bullosa-sensorineural deafness syndrome 1 shared geneCD151 Related via 1 shared gene including CD151. Epidermolysis bullosa 1 shared geneCD151 Related via 1 shared gene including CD151.