Cone dystrophy, x-linked

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CONE DYSTROPHY, X-LINKED, 1
C1844777
RPGR Unknown — 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.