Oguchi disease

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
OGUCHI DISEASE
75382C1306122MESH:C537743MONDO:0019152
SAG Causal
15295660 22419846 7670478 9565049
CTD, ClinVar, Disgenet, Orphanet
OGUCHI DISEASE-1
MONDO:0009775
SAG Causal
7670478 9565049 9452120 22665972 15234147
ClinVar, GWAS catalog
OGUCHI DISEASE-2
MONDO:0013259
GRK1 Causal
9020843 17070587 26349155
ClinVar, GWAS catalog, ClinGen
All14 Causal2 Unknown14
Related Diseases Diseases that share the most curated genes with Oguchi disease.
5 View disease cluster →
Congenital stationary night blindness 10 shared genesCACNA1F, PDE6B, TRPM1, RHO, GNB3, GNAT1, GRM6, LRIT3, NYX, SLC24A1 Related via 10 shared genes including CACNA1F, PDE6B, TRPM1. Night blindness, congenital stationary 13 shared genesCACNA1F, PDE6B, TRPM1, GUCY2D, RHO, GNB3, GNAT1, SAG, GRM6, LRIT3, NYX, SLC24A1 +1 more Related via 13 shared genes including CACNA1F, PDE6B, TRPM1. inherited retinal dystrophy 3 shared genesPDE6B, GNAT1, SLC24A1 Related via 3 shared genes including PDE6B, GNAT1, SLC24A1. Cone dystrophy 5 shared genesCACNA1F, PDE6B, GUCY2D, RHO, SAG Related via 5 shared genes including CACNA1F, PDE6B, GUCY2D. Aland island eye disease 1 shared geneCACNA1F Related via 1 shared gene including CACNA1F.