SELENON-related myopathy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
SELENON-related myopathy
SELENON Causal
20937510 23394784 31066047 17951086 11528383 30642275 32154989 15792869 26780752 29172004 12192640 28688748 15668457 16498447 29850975 15961312 25808192 21670436 28558865 28606403 26841830
ClinGen —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with SELENON-related myopathy.
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Multiminicore myopathy 1 shared geneSELENON Related via 1 shared gene including SELENON. Eichsfeld type congenital muscular dystrophy 1 shared geneSELENON Related via 1 shared gene including SELENON. Rigid spine muscular dystrophy 1 shared geneSELENON Related via 1 shared gene including SELENON. Congenital fiber type disproportion myopathy 1 shared geneSELENON Related via 1 shared gene including SELENON. Congenital myopathy 1 shared geneSELENON Related via 1 shared gene including SELENON.