Retinal disorder

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
retinal disorder
MONDO_0005283
CYP2U1 Unknown
23176821 26914923 29034544 34546337 39605873 38058766 34828401 33107650
Open Targets
DYRK1A Unknown
40405340 33159716 19081073 36736451
Open Targets
GPATCH11 Unknown
39572588
Open Targets —
SPG11 Unknown
39391989 36343909 19194956 38613257
Open Targets
UNC119 Unknown
30910914 23563732 35947183 11006213 27079236
Open Targets —
VSX2 Unknown
24001013 20414678 36264558
Open Targets —
All6 Causal0 Unknown6
Related Diseases Diseases that share the most curated genes with Retinal disorder.
5 View disease cluster →
Hereditary spastic paraplegia 11 1 shared geneSPG11 Related via 1 shared gene including SPG11. Microphthalmia with cataracts and iris abnormalities 1 shared geneVSX2 Related via 1 shared gene including VSX2. Microphthalmia/coloboma 3 1 shared geneVSX2 Related via 1 shared gene including VSX2. Microphthalmia, isolated 2 1 shared geneVSX2 Related via 1 shared gene including VSX2. Spastic paraplegia 56, autosomal recessive 1 shared geneCYP2U1 Related via 1 shared gene including CYP2U1.