OPA1-related optic atrophy with or without extraocular features

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
OPA1-related optic atrophy with or without extraocular features
OPA1 Causal — ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with OPA1-related optic atrophy with or without extraocular features.
5 View disease cluster →
Dominant hereditary optic atrophy 1 shared geneOPA1 Related via 1 shared gene including OPA1. Blepharoptosis 1 shared geneOPA1 Related via 1 shared gene including OPA1. Centronuclear myopathy 1 shared geneOPA1 Related via 1 shared gene including OPA1. Ventricular remodeling 1 shared geneOPA1 Related via 1 shared gene including OPA1. Stargardt disease 1 shared geneOPA1 Related via 1 shared gene including OPA1.