Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome

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Subtype of: Global developmental delay · Optic atrophy
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome
MONDO_0034092
FDXR Causal
28965846 30250212 32499495 33938912
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome.
5 View disease cluster →
Optic atrophy mitochondrial dysfunction syndrome 1 shared geneFDXR Related via 1 shared gene including FDXR. Multiple mitochondrial dysfunctions syndrome 9b 1 shared geneFDXR Related via 1 shared gene including FDXR. Auditory neuropathy with optic atrophy 1 shared geneFDXR Related via 1 shared gene including FDXR. Auditory neuropathy 1 shared geneFDXR Related via 1 shared gene including FDXR. Optic atrophy 1 shared geneFDXR Related via 1 shared gene including FDXR.