myopathy, centronuclear, 6, with fiber-type disproportion

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Myopathy, centronuclear, 6, with fiber-type disproportion
MAP3K20 Causal
27816943 30237576
ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with myopathy, centronuclear, 6, with fiber-type disproportion.
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Split hand-foot malformation 1 shared geneMAP3K20 Related via 1 shared gene including MAP3K20. Ectrodactyly 1 shared geneMAP3K20 Related via 1 shared gene including MAP3K20. Congenital fiber type disproportion myopathy 1 shared geneMAP3K20 Related via 1 shared gene including MAP3K20. Centronuclear myopathy 1 shared geneMAP3K20 Related via 1 shared gene including MAP3K20. Hemorrhoid 1 shared geneMAP3K20 Related via 1 shared gene including MAP3K20.