Leber optic atrophy and dystonia

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Subtype of: Optic atrophy
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Leber optic atrophy and dystonia
MONDO_0020478
ND3 Unknown
19458970 30199507 39923090
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Leber optic atrophy and dystonia.
5 View disease cluster →
Neuropathy, ataxia, and retinitis pigmentosa 1 shared geneND3 Related via 1 shared gene including ND3. Cleft palate and bilateral cleft lip 1 shared geneND3 Related via 1 shared gene including ND3. Melas syndrome 1 shared geneND3 Related via 1 shared gene including ND3. Postaxial polydactyly 1 shared geneND3 Related via 1 shared gene including ND3. Leber hereditary optic neuropathy 1 shared geneND3 Related via 1 shared gene including ND3.