Retinal degeneration

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
RETINAL DEGENERATION
MESH:D012162
RPE65 Causal
24849605 32971638
CTD
All37 Causal1 Unknown36
Related Diseases Diseases that share the most curated genes with Retinal degeneration.
5 View disease cluster →
Cone-rod dystrophy 9 shared genesPDE6B, CRX, RPE65, NMNAT1, RHO, RPGR, RAX2, UBAP1L, RDH12 Related via 9 shared genes including PDE6B, CRX, RPE65. Leber congenital amaurosis 8 shared genesPDE6B, CRX, RPE65, NMNAT1, RPGRIP1L, AHI1, RPGR, RDH12 Related via 8 shared genes including PDE6B, CRX, RPE65. Night blindness, congenital stationary 4 shared genesPDE6B, RHO, GNAT1, RPGR Related via 4 shared genes including PDE6B, RHO, GNAT1. Stargardt disease 4 shared genesCRX, RPE65, RHO, RDH12 Related via 4 shared genes including CRX, RPE65, RHO. Congenital stationary night blindness 3 shared genesPDE6B, RHO, GNAT1 Related via 3 shared genes including PDE6B, RHO, GNAT1.