optic atrophy 13 with retinal and foveal abnormalities

Log in to bookmark this disease

Bookmark This Disease

Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Optic atrophy 13 with retinal and foveal abnormalities
SSBP1 Causal
31550237 31298765 31550240
ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with optic atrophy 13 with retinal and foveal abnormalities.
5 View disease cluster →
Dermatologic disorder 1 shared geneSSBP1 Related via 1 shared gene including SSBP1. Cone-rod dystrophy 1 shared geneSSBP1 Related via 1 shared gene including SSBP1. Leigh syndrome 1 shared geneSSBP1 Related via 1 shared gene including SSBP1. Isolated sensorineural deafness 1 shared geneSSBP1 Related via 1 shared gene including SSBP1. Skin disease 1 shared geneSSBP1 Related via 1 shared gene including SSBP1.