Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome

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Subtype of: Mitochondrial myopathy
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome
MONDO_0044714
MSTO1 Causal
29339779 28544275 31130378 28554942 31604776 37431817 31463572 30684668
Open Targets —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome.
5 View disease cluster →
Mitochondrial myopathy 1 shared geneMSTO1 Related via 1 shared gene including MSTO1. Neuromuscular disease 1 shared geneMSTO1 Related via 1 shared gene including MSTO1. Myopathy 1 shared geneMSTO1 Related via 1 shared gene including MSTO1. Mitochondrial disease 1 shared geneMSTO1 Related via 1 shared gene including MSTO1. Breast cancer 1 shared geneMSTO1 Related via 1 shared gene including MSTO1.