Autosomal recessive optic atrophy, OPA7 type

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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
autosomal recessive optic atrophy, OPA7 type
227976MONDO:0013069
TMEM126A Causal — ClinGen —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Autosomal recessive optic atrophy, OPA7 type.
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Auditory neuropathy with optic atrophy 1 shared geneTMEM126A Related via 1 shared gene including TMEM126A. Optic atrophy 1 shared geneTMEM126A Related via 1 shared gene including TMEM126A. Mitochondrial disease 1 shared geneTMEM126A Related via 1 shared gene including TMEM126A. Retinitis pigmentosa 1 shared geneTMEM126A Related via 1 shared gene including TMEM126A. Melanoma 1 shared geneTMEM126A Related via 1 shared gene including TMEM126A.