AFG3L2-related optic atrophy and/or spastic ataxia spectrum

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
AFG3L2-related optic atrophy and/or spastic ataxia spectrum
AFG3L2 Unknown — ClinGen
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with AFG3L2-related optic atrophy and/or spastic ataxia spectrum.
5 View disease cluster →
Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome 1 shared geneAFG3L2 Related via 1 shared gene including AFG3L2. Chorea 1 shared geneAFG3L2 Related via 1 shared gene including AFG3L2. Hyperkinesia 1 shared geneAFG3L2 Related via 1 shared gene including AFG3L2. Glycogen storage disease 1 shared geneAFG3L2 Related via 1 shared gene including AFG3L2. Spastic ataxia 1 shared geneAFG3L2 Related via 1 shared gene including AFG3L2.