Retinal cone dystrophy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
RETINAL CONE DYSTROPHY 2
C1866293MESH:C538363
BEST1 Unknown — Disgenet
GUCY2D Unknown — CTD, Disgenet
KCNV2 Unknown — Disgenet
RETINAL CONE DYSTROPHY 3A
610024C1864900MESH:C566483MONDO:0012398
PDE6H Unknown
15629837 22901948
CTD, ClinVar, Disgenet, GenCC, HPO
RETINAL CONE DYSTROPHY 3B
610356C1835897MESH:C563678
KCNV2 Unknown
16909397 19952985
CTD, Disgenet, HPO
RETINAL CONE DYSTROPHY 4
610478C1864849MESH:C566470MONDO:0012507
CACNA2D4 Unknown
17033974 26560832
CTD, ClinVar, Disgenet, GWAS catalog, HPO
All5 Causal0 Unknown5
Related Diseases Diseases that share the most curated genes with Retinal cone dystrophy.
5 View disease cluster →
GUCY2D-related dominant retinopathy 1 shared geneGUCY2D Related via 1 shared gene including GUCY2D. GUCY2D-related recessive retinopathy 1 shared geneGUCY2D Related via 1 shared gene including GUCY2D. CACNA2D4-related retinopathy 1 shared geneCACNA2D4 Related via 1 shared gene including CACNA2D4. Vitreoretinochoroidopathy 1 shared geneBEST1 Related via 1 shared gene including BEST1. Choroidal dystrophy 1 shared geneGUCY2D Related via 1 shared gene including GUCY2D.