Retinal dystrophy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
retinal dystrophy
MONDO_0019118
ASRGL1 Unknown
27106100
Open Targets
DTHD1 Unknown
23105016
Open Targets —
GUCA1B Unknown
15452722 21405999
Open Targets
MORC2 Unknown
26659848 32693025 39143067 40302207 36791574
Open Targets
POC5 Unknown
40590205 29272404
Open Targets —
SCLT1 Unknown
28005958 41963357 37734845
Open Targets
SGSH Unknown
31718697 32195255
Open Targets
TRNL1 Unknown
18332310 23806424
Open Targets
All17 Causal9 Unknown8
Related Diseases Diseases that share the most curated genes with Retinal dystrophy.
5 View disease cluster →
Dominant retinopathy 2 shared genesRPE65, SNRNP200 Related via 2 shared genes including RPE65, SNRNP200. Cone-rod dystrophy 6 shared genesRPGRIP1, RPE65, CLN3, SCLT1, ARL6, GUCA1B Related via 6 shared genes including RPGRIP1, RPE65, CLN3. Nystagmus 4 shared genesRPGRIP1, RPE65, SCLT1, SGSH Related via 4 shared genes including RPGRIP1, RPE65, SCLT1. Retinitis pigmentosa with choroidal involvement 1 shared geneRPE65 Related via 1 shared gene including RPE65. Abnormal muscle physiology 1 shared genePOC5 Related via 1 shared gene including POC5.