Cone dystrophy, x-linked

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
CONE DYSTROPHY 5, X-LINKED
C3887937
OPN1MW Causal — Disgenet
All2 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Cone dystrophy, x-linked.
5 View disease cluster →
red-green color blindness 1 shared geneOPN1MW Related via 1 shared gene including OPN1MW. Ciliary dyskinesia with retinitis pigmentosa 1 shared geneRPGR Related via 1 shared gene including RPGR. Retinitis pigmentosa, x-linked, and sinorespiratory infections with or without deafness 1 shared geneRPGR Related via 1 shared gene including RPGR. RPGR-related retinopathy 1 shared geneRPGR Related via 1 shared gene including RPGR. Cone monochromatism 1 shared geneOPN1MW Related via 1 shared gene including OPN1MW.