Congenital myopathy 3 with rigid spine

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Subtype of: Congenital myopathy
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Congenital myopathy 3 with rigid spine
MONDO_0011271
SELENON Unknown
20301467 32796131 30642275 18713863 11528383 15122708 15668457 16365872 19067361 12192640
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Congenital myopathy 3 with rigid spine.
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Multiminicore myopathy 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. Muscular dystrophy 1 shared geneSELENON Related via 1 shared gene including SELENON.